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Section 53

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References:

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Elnagar, A.Y.; Wali, V.B.; Sylvester, P.W.; El Sayed, K.A. 2010: Design and preliminary structure-activity relationship of redox-silent semisynthetic tocotrienol analogues as inhibitors for breast cancer proliferation and invasion. Bioorganic and Medicinal Chemistry 18(2): 755-768
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Piccinelli, R.; Pandelova, M.; Le Donne, C.; Ferrari, M.; Schramm, K-W.; Leclercq, C. 2010: Design and preparation of market baskets of European Union commercial baby foods for the assessment of infant exposure to food chemicals and to their effects. Food Additives and Contaminants. Part A Chemistry Analysis Control Exposure and Risk Assessment 27(10): 1337-1351
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Deslandes, S.; Baudet, A.; Berthelot, M.; Grancher, S.; Moissenet, F. 2012: Design and prototyping of a system for ankle spasticity quantification. Computer Methods in Biomechanics and Biomedical Engineering 15 Suppl. 1: 237-239
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Ordoñez, A.A.L.; Ordoñez, R.M.; Zampini, I.C.; Isla, M.ía.I. 2009: Design and quality control of a pharmaceutical formulation containing natural products with antibacterial, antifungal and antioxidant properties. International Journal of Pharmaceutics 378(1-2): 51-58
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Margolis, K.L.; Kerby, T.J.; Asche, S.E.; Bergdall, A.R.; Maciosek, M.V.; O'Connor, P.J.; Sperl-Hillen, J.M. 2012: Design and rationale for Home Blood Pressure Telemonitoring and Case Management to Control Hypertension (HyperLink): a cluster randomized trial. Contemporary Clinical Trials 33(4): 794-803
Klausen, S.H.; Mikkelsen, U.R.; Hirth, A.; Wetterslev, J.ør.; Kjærgaard, H.; Søndergaard, L.; Andersen, L.L. 2012: Design and rationale for the PREVAIL study: effect of e-Health individually tailored encouragements to physical exercise on aerobic fitness among adolescents with congenital heart disease--a randomized clinical trial. American Heart Journal 163(4): 549-556
Bonaca, M.P.; Bhatt, D.L.; Braunwald, E.; Cohen, M.; Steg, P.Gabriel.; Storey, R.F.; Held, P.; Jensen, E.C.; Sabatine, M.S. 2014: Design and rationale for the Prevention of Cardiovascular Events in Patients With Prior Heart Attack Using Ticagrelor Compared to Placebo on a Background of Aspirin-Thrombolysis in Myocardial Infarction 54 (PEGASUS-TIMI 54) trial. American Heart Journal 167(4): 437-444.E5
Lencioni, R.; Marrero, J.; Venook, A.; Ye, S.-L.; Kudo, M. 2010: Design and rationale for the non-interventional Global Investigation of Therapeutic DEcisions in Hepatocellular Carcinoma and of its Treatment with Sorafenib (GIDEON) study. International Journal of Clinical Practice 64(8): 1034-1041
Mehta, S.R.; Bassand, J.-P.; Chrolavicius, S.; Diaz, R.; Fox, K.A.A.; Granger, C.B.; Jolly, S.; Rupprecht, H.-J.; Widimsky, P.; Yusuf, S.; Mehta, S.R.; Ajani, A.; Avezum, A.; Bassand, J.P.; Boden, W.E.; Budaj, A.; Cardona, E.; Chrolavicius, S.; Col, J.; Commerford, P.; Di Pasquale, G.; Diaz, R.; Eha, J.; Eikelboom, J.W.; Faxon, D.P.; Flather, M.; Foley, D.; Fox, K.A.A.; Franzosi, M.G.; Granger, C.B.; Gupta, M.; Jolly, S.; Joyner, C.; Karatzas, N.; Kastrati, A.; Kim, J.H.; Koh, T.H.; Lanas, F.; Lewis, B.; Macaya, C.; Moccetti, T.; Montalescot, G.; Niemela, K.; Ongen, Z.; Orlandini, A.; Pais, P.; Peters, R.J.G.; Piegas, L.; Probstfield, J.; Rankin, J.; Ruda, M.; Rumboldt, Z.; Rupprecht, H.J.; Steg, P.G.; Tanguay, J.-F.; Valentin, V.; Varigos, 2008: Design and rationale of CURRENT-OASIS 7: a randomized, 2 x 2 factorial trial evaluating optimal dosing strategies for clopidogrel and aspirin in patients with ST and non-ST-elevation acute coronary syndromes managed with an early invasive strategy. American Heart Journal 156(6): 1080-1088.E1
Hájek, R.; Bryce, R.; Ro, S.; Klencke, B.; Ludwig, H. 2012: Design and rationale of FOCUS (PX-171-011): a randomized, open-label, phase 3 study of carfilzomib versus best supportive care regimen in patients with relapsed and refractory multiple myeloma (R/R MM). Bmc Cancer 12: 415
Huisman, M.V.; Lip, G.Y.H.; Diener, H.C.; Dubner, S.J.; Halperin, J.L.; Ma, C.S.; Rothman, K.J.; Teutsch, C.; Zint, K.; Ackermann, D.; Clemens, A.; Bartels, D.B. 2014: Design and rationale of Global Registry on Long-Term Oral Antithrombotic Treatment in Patients with Atrial Fibrillation: a global registry program on long-term oral antithrombotic treatment in patients with atrial fibrillation. American Heart Journal 167(3): 329-334
Ando, K.; Haneda, M.; Ito, S.; Kashihara, N.; Node, K.; Nangaku, M.; Shimosawa, T.; Kishimoto, J.; Fujita, T. 2011: Design and rationale of Japanese evaluation between Formula of Azelnidipine and amlodipine add on olmesartan to get antialbuminuric effect study (J-FLAG) : evaluation of the antialbuminuric effects between calcium channel blocker with sympatholytic action in hypertensive patients with diabetes and albuminuria. Cardiovascular Drugs and Therapy 25(4): 341-347
Dean, O.M.; Turner, A.; Malhi, G.S.; Ng, C.; Cotton, S.M.; Dodd, S.; Sarris, J.; Samuni, Y.; Tanious, M.; Dowling, N.; Waterdrinker, A.; Smith, D.; Berk, M. 2015: Design and rationale of a 16-week adjunctive randomized placebo-controlled trial of mitochondrial agents for the treatment of bipolar depression. Revista Brasileira de Psiquiatria 37(1): 3-12
Rutledge, T.; Nidich, S.; Schneider, R.H.; Mills, P.J.; Salerno, J.; Heppner, P.; Gomez, M.A.; Gaylord-King, C.; Rainforth, M. 2014: Design and rationale of a comparative effectiveness trial evaluating transcendental meditation against established therapies for PTSD. Contemporary Clinical Trials 39(1): 50-56
Dubé, M-Pierre.; Bigras, J-Luc.; Thibeault, M.; Bureau, N.; Chetaille, P.; Richter, A.; Mercier, J.; Bellavance, M.; Rohlicek, C.; Rozen, R.; Nemer, M.; Khairy, P.; Gendron, R.; Andelfinger, G. 2011: Design and rationale of a genetic cohort study on congenital cardiac disease: experiences from a multi-institutional platform in Quebec. Cardiology in the Young 21(6): 654-664
Goodrich, D.E.; Kilbourne, A.M.; Lai, Z.; Post, E.P.; Bowersox, N.W.; Mezuk, B.; Schumacher, K.; Bramlet, M.; Welsh, D.E.; Bauer, M.S. 2012: Design and rationale of a randomized controlled trial to reduce cardiovascular disease risk for patients with bipolar disorder. Contemporary Clinical Trials 33(4): 666-678
Ohye, R.G.; Gaynor, J.W.; Ghanayem, N.S.; Goldberg, C.S.; Laussen, P.C.; Frommelt, P.C.; Newburger, J.W.; Pearson, G.D.; Tabbutt, S.; Wernovsky, G.; Wruck, L.M.; Atz, A.M.; Colan, S.D.; Jaggers, J.; McCrindle, B.W.; Prakash, A.; Puchalski, M.D.; Sleeper, L.A.; Stylianou, M.P.; Mahony, L.; Pearson, G.; Pemberton, V.; Kavey, R.-E.; Massicot-Fisher, J.; Mathis, M.; Stylianou, M.; Mahony, L.; Sleeper, L.; Colan, S.D.; Connell, P.; Murtov, V.; Wruck, L.; Virzi, L.; Teitel, D.F.; Newburger, J.; Laussen, P.; del Nido, P.; Breitbart, R.; Levine, J.; McGrath, E.; Dunbar-Masterson, C.; Hsu, D.; Prakash, A.; Mosca, R.; Servedio, D.; Vetter, V.L.; Tabbutt, S.; Gaynor, J.W.; Nolan, M.; Piacentino, S.; Benson, D.W.; Dent, C.; Bogenschutz, L.; Barnard, T. 2008: Design and rationale of a randomized trial comparing the Blalock-Taussig and right ventricle-pulmonary artery shunts in the Norwood procedure. Journal of Thoracic and Cardiovascular Surgery 136(4): 968-975
Amann, B.; Lüdemann, C.; Rückert, R.; Lawall, H.; Liesenfeld, B.; Schneider, M.; Schmidt-Lucke, J. 2008: Design and rationale of a randomized, double-blind, placebo-controlled phase IIi study for autologous bone marrow cell transplantation in critical limb ischemia: the BONe Marrow Outcomes Trial in Critical Limb Ischemia (BONMOT-CLI). VASA. Zeitschrift für Gefasskrankheiten 37(4): 319-325
Zamorano, J.é; Erdine, S.; Lopez, A.P.; Kim, J.-H.; Al Khadra, A.; Westergaard, M.; Sutradhar, S.; Yunis, C.; Gamboa-Garro, R.; Moya-Rodriguez, J.; Ramirez, L.C.; Slon-Hitti, C.; Tortos-Guzman, J.E.; Vinocour-Fornieri, M.; Bokarica, D.; Bezdrov, M.; Car, I.; Cikac, T.; Cop, R.; Hrandek, B.H.; Javoric, J.; Kotur, G.; Kranjcevic, K.; Lazic, G.; Maravic, Z.; Margetic, S.; Primorac, L.; Prlina, M.; Smiciklas, N.F.; Stritof, M.; Vivoda, Z.B.; Vrdoljak, D.; Herle, P.; Kos, P.; Marek, V.; Miskovska, Z.; Moravcikova, D.; Motlikova, E.; Nejedla, A.; Seifert, B.; Skala, B.; Vecerek, M.; Winklerova, J.; Almonte, C.; Gonzalez-Medina, A.; Pichardo, R.; Chandradin, C.; Harahap, M.L.; Kusmana, D.; Lukito, A.A.; Makmun, L.H.; Martanto, E.; Rifqi, S.; Yogi 2010: Design and rationale of a real-life study to compare treatment strategies for cardiovascular risk factors: the CRUCIAL study. Postgraduate Medicine 122(2): 7-15
Curtis, L.H.; Mi, X.; Qualls, L.G.; Hammill, B.G.; Hammill, S.C.; Heidenreich, P.A.; Masoudi, F.A.; Setoguchi, S.; Hernandez, A.F.; Fonarow, G.C. 2012: Design and rationale of a retrospective clinical effectiveness study of aldosterone antagonist therapy in patients with heart failure. American Heart Journal 163(6): 946-953.E1
Ge, J.; Kim, Y.-J.; Jang, Y.-S.; Zhu, J.; Marschner, I.C.; Lam, W. 2010: Design and rationale of a study in Asia of atorvastatin pretreatment in patients undergoing percutaneous coronary intervention for non-ST elevation acute coronary syndromes. Journal of Cardiology 55(3): 303-308
Jhamb, M.; Tamura, M.K.; Gassman, J.; Garg, A.X.; Lindsay, R.M.; Suri, R.S.; Ting, G.; Finkelstein, F.O.; Beach, S.; Kimmel, P.L.; Unruh, M. 2011: Design and rationale of health-related quality of life and patient-reported outcomes assessment in the Frequent Hemodialysis Network trials. Blood Purification 31(1-3): 151-158
Gaies, M.G.; Langer, M.; Alexander, J.; Steil, G.M.; Ware, J.; Wypij, D.; Laussen, P.C.; Newburger, J.W.; Goldberg, C.S.; Pigula, F.A.; Shukla, A.C.; Duggan, C.P.; Agus, M.S.D.; Costello, J.M.; Curley, M.A.; Del Nido, P.J.; Sadhwani, A.; Gaies, M.G.; Goldberg, C.S.; Langer, M.; Alexander, J.; Steil, G.M.; Ware, J.; Wypij, D.; Laussen, P.C.; Newburger, J.W.; Pigula, F.A.; Shukla, A.C.; Duggan, C.P.; Agus, M.S.D. 2013: Design and rationale of safe pediatric euglycemia after cardiac surgery: a randomized controlled trial of tight glycemic control after pediatric cardiac surgery. Pediatric Critical Care Medicine: a Journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies 14(2): 148-156
Gibson, C.Michael.; Krucoff, M.; Kirtane, A.J.; Rao, S.V.; Mackall, J.A.; Matthews, R.; Saba, S.; Waksman, R.; Holmes, D. 2014: Design and rationale of the ANALYZE ST study: a prospective, nonrandomized, multicenter ST monitoring study to detect acute coronary syndrome events in implantable cardioverter-defibrillator patients. American Heart Journal 168(4): 424-429.E1
de Andrade, P.Beraldo.; E Mattos, L.Alberto.Piva.; Tebet, M.André.; Rinaldi, Fábio.Salerno.; Esteves, Vícius.Cardozo.; Nogueira, E.Ferreira.; França, Jão.Ítalo.Dias.; de Andrade, Mônica.Vieira.Athanazio.; Barbosa, R.Alves.; Labrunie, Aé.; Abizaid, A.Antônio.Cunha.; Sousa, A.Guerra.de.Moraes.Rego. 2013: Design and rationale of the AngioSeal versus the Radial approach In acute coronary SyndromE (ARISE) trial: a randomized comparison of a vascular closure device versus the radial approach to prevent vascular access site complications in non-ST-segment elevation acute coronary syndrome patients. Trials 14: 435
Melloni, C.; Fier, I.; Roach, J.; Kosinski, A.S.; Broderick, S.; Sigmon, K.; Myles, S.; Becker, R.C.; Rao, S.V. 2009: Design and rationale of the Evaluation of M118 IN pErcutaNeous Coronary int Ervention (EMINENCE) trial. American Heart Journal 158(5): 726-733
Cho, L.; Rocco, M.; Colquhoun, D.; Sullivan, D.; Rosenson, R.S.; Dent, R.; Xue, A.; Scott, R.; Wasserman, S.M.; Stroes, E. 2014: Design and rationale of the GAUSS-2 study trial: a double-blind, ezetimibe-controlled phase 3 study of the efficacy and tolerability of evolocumab (AMG 145) in subjects with hypercholesterolemia who are intolerant of statin therapy. Clinical Cardiology 37(3): 131-139
Kohli, P.; Desai, N.R.; Giugliano, R.P.; Kim, J.B.; Somaratne, R.; Huang, F.; Knusel, B.; McDonald, S.; Abrahamsen, T.; Wasserman, S.M.; Scott, R.; Sabatine, M.S. 2012: Design and rationale of the LAPLACE-TIMi 57 trial: a phase II, double-blind, placebo-controlled study of the efficacy and tolerability of a monoclonal antibody inhibitor of PCSK9 in subjects with hypercholesterolemia on background statin therapy. Clinical Cardiology 35(7): 385-391
Straka, Z.ěk.; Budera, P.; Osmančík, P.; Vaněk, T.áš; Hulman, M.; Smíd, M.; Malý, M.; Widimský, P. 2013: Design and rationale of the PRAGUE-12 trial: a large, prospective, randomized, multicenter trial that compares cardiac surgery with left atrial surgical ablation with cardiac surgery without ablation in patients with coronary and/or valvular heart disease plus atrial fibrillation. Clinical Cardiology 36(1): 1-5
Weatherley, B.D.; Cotter, G.; Dittrich, H.C.; DeLucca, P.; Mansoor, G.A.; Bloomfield, D.M.; Ponikowski, P.; O'Connor, C.M.; Metra, M.; Massie, B.M.; Adams, K.; Allall, O.; Ambrosia, A.; Amosova, K.; Amuchastegui, M.; Aronson, D.; Arutyunov, G.; Balbi, M.; Banerjee, P.; Bart, B.; Bellersen, L.; Belohlávek, J.; Bensimhon, D.; Billberg, E.B.; Bilsker, M.; Bleyer, F.L.; Böhm, M.; Boldueva, S.; Bourge, R.; Bozkurt, B.; Butnaru, A.; Cabuay, B.; Caccavo, A.; Chandrasekaran, S.; Chiong, J.; Chung, E.; Cleland, J.G.; Cohen-Solal, A.; Colque, R.M.A.; Colvin-Adams, M.; Convens, C.; Cooke, R.; Cornel, J.H.; Czerska, B.; Dahlström, U.; Diez, M.; Dluzniewski, M.; El Allaf, D.; Dorobantu C, M.; Ducharme, A.; Dunlap, M.; Dunlap, S.; Elkayam, U.; Ez 2010: Design and rationale of the PROTECT study: a placebo-controlled randomized study of the selective A1 adenosine receptor antagonist rolofylline for patients hospitalized with acute decompensated heart failure and volume overload to assess treatment effect on congestion and renal function. Journal of Cardiac Failure 16(1): 25-35
Alphs, L.; Mao, L.; Rodriguez, S.C.; Hulihan, J.; Starr, H.Lynn. 2014: Design and rationale of the Paliperidone Palmitate Research in Demonstrating Effectiveness (PRIDE) study: a novel comparative trial of once-monthly paliperidone palmitate versus daily oral antipsychotic treatment for delaying time to treatment failure in persons with schizophrenia. Journal of Clinical Psychiatry 75(12): 1388-1393
Melloni, C.; Rao, S.V.; Povsic, T.J.; Melton, L.; Kim, R.J.; Kilaru, R.; Patel, M.R.; Talan, M.; Ferrucci, L.; Longo, D.L.; Lakatta, E.G.; Najjar, S.S.; Harrington, R.A. 2010: Design and rationale of the Reduction of Infarct Expansion and Ventricular Remodeling with Erythropoietin after Large Myocardial Infarction (REVEAL) trial. American Heart Journal 160(5): 795-803.E2
Jolly, S.S.; Cairns, J.; Yusuf, S.; Meeks, B.; Shestakovska, O.; Thabane, L.; Niemelä, K.; Steg, P.G.; Bertrand, O.F.; Rao, S.V.; Avezum, A.; Cantor, W.J.; Pancholy, S.B.; Moreno, R.; Gershlick, A.; Bhindi, R.; Welsh, R.C.; Cheema, A.N.; Lavi, S.; Rokoss, M.; Džavík, V.ír. 2014: Design and rationale of the TOTAL trial: a randomized trial of routine aspiration ThrOmbecTomy with percutaneous coronary intervention (PCI) versus PCi ALone in patients with ST-elevation myocardial infarction undergoing primary PCi. American Heart Journal 167(3): 315-321.E1
Klomp, M.; Beijk, M.A.M.; Verouden, N.J.W.; Tijssen, J.G.P.; de Winter, R.J.; Debbas; Benit; Coussement; Ylitalo; Sia; Teiger; Grollier; Montalescot; Gommeaux; Machecourt; Bea; von Scheidt; Pfeifer; Khattab; Rittger; Sick; Radke; Wiemer; Braun; Manginas; Manolis; Tsui; Erglis; Sim; Varma; Ionescu; Menown; Koolen; den Heijer; Schotborgh; de Winter 2009: Design and rationale of the TRI-stent adjudication study (TRIAS) program. American Heart Journal 158(4): 527-532.E1
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Deng, X.-Q.; Wei, C.-X.; Li, F.-N.; Sun, Z.-G.; Quan, Z.-S. 2010: Design and synthesis of 10-alkoxy-5, 6-dihydro-triazolo[4,3-d]benzo[f][1,4]oxazepine derivatives with anticonvulsant activity. European Journal of Medicinal Chemistry 45(7): 3080-3086
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Kumar, A.; Sharma, S.; Tripathi, V.D.; Maurya, R.A.; Srivastava, S.P.; Bhatia, G.; Tamrakar, A.K.; Srivastava, A.K. 2010: Design and synthesis of 2,4-disubstituted polyhydroquinolines as prospective antihyperglycemic and lipid modulating agents. Bioorganic and Medicinal Chemistry 18(11): 4138-4148
Hsin, L.-W.; Chang, L.-T.; Rothman, R.B.; Dersch, C.M.; Jacobson, A.E.; Rice, K.C. 2008: Design and synthesis of 2- and 3-substituted-3-phenylpropyl analogs of 1-[2-[bis(4-fluorophenyl)methoxy]ethyl]-4-(3-phenylpropyl)piperazine and 1-[2-(diphenylmethoxy)ethyl]-4-(3-phenylpropyl)piperazine: role of amino, fluoro, hydroxyl, methoxyl, methyl, methylene, and oxo substituents on affinity for the dopamine and serotonin transporters. Journal of Medicinal Chemistry 51(9): 2795-2806
Nikalje, A.P.G.; Khan, F.K.; Ghodke, M. 2011: Design and synthesis of 2-(1, 3-dioxoisoindolin-2-yl)-N-(4-oxo-2-substitutedthiazolidin-3-yl) acetamide derivatives as potential anticonvulsant agents. European Journal of Medicinal Chemistry 46(11): 5448-5455
Rawal, R.K.; Tripathi, R.; Katti, S.B.; Pannecouque, C.; De Clercq, E. 2008: Design and synthesis of 2-(2,6-dibromophenyl)-3-heteroaryl-1,3-thiazolidin-4-ones as anti-HIV agents. European Journal of Medicinal Chemistry 43(12): 2800-2806
Huang, S.-M.; Cheng, Y.-Y.; Chen, M.-H.; Huang, C.-H.; Huang, L.-J.; Hsu, M.-H.; Kuo, S.-C.; Lee, K.-H. 2013: Design and synthesis of 2-(3-alkylaminophenyl)-6-(pyrrolidin-1-yl)quinolin-4-ones as potent antitumor agents. Bioorganic and Medicinal Chemistry Letters 23(3): 699-701
Chang, Y.-H.; Hsu, M.-H.; Wang, S.-H.; Huang, L.-J.; Qian, K.; Morris-Natschke, S.L.; Hamel, E.; Kuo, S.-C.; Lee, K.-H. 2009: Design and synthesis of 2-(3-benzo[b]thienyl)-6,7-methylenedioxyquinolin-4-one analogues as potent antitumor agents that inhibit tubulin assembly. Journal of Medicinal Chemistry 52(15): 4883-4891
Qian, Y.; Bolin, D.; Conde-Knape, K.; Gillespie, P.; Hayden, S.; Huang, K.-S.; Olivier, A.ée.R.; Sato, T.; Xiang, Q.; Yun, W.; Zhang, X. 2013: Design and synthesis of 2-N-substituted indazolone derivatives as non-carboxylic acid glycogen synthase activators. Bioorganic and Medicinal Chemistry Letters 23(10): 2936-2940
Gao, Q.; Wu, X.; Jia, F.; Liu, M.; Zhu, Y.; Cai, Q.; Wu, A. 2013: Design and synthesis of 2-acylbenzothiazoles via in situ cross-trapping strategy from benzothiazoles with aryl ketones. Journal of Organic Chemistry 78(6): 2792-2797
Zhou, D.; Lee, H.; Rothfuss, J.M.; Chen, D.L.; Ponde, D.E.; Welch, M.J.; Mach, R.H. 2009: Design and synthesis of 2-amino-4-methylpyridine analogues as inhibitors for inducible nitric oxide synthase and in vivo evaluation of [18F]6-(2-fluoropropyl)-4-methyl-pyridin-2-amine as a potential PET tracer for inducible nitric oxide synthase. Journal of Medicinal Chemistry 52(8): 2443-2453
Suda, A.; Kawasaki, K.-i.; Komiyama, S.; Isshiki, Y.; Yoon, D.-O.; Kim, S.-J.; Na, Y.-J.; Hasegawa, K.; Fukami, T.A.; Sato, S.; Miura, T.; Ono, N.; Yamazaki, T.; Saitoh, R.; Shimma, N.; Shiratori, Y.; Tsukuda, T. 2014: Design and synthesis of 2-amino-6-(1H,3H-benzo[de]isochromen-6-yl)-1,3,5-triazines as novel Hsp90 inhibitors. Bioorganic and Medicinal Chemistry 22(2): 892-905
Hanan, E.J.; Fucini, R.V.; Romanowski, M.J.; Elling, R.A.; Lew, W.; Purkey, H.E.; VanderPorten, E.C.; Yang, W. 2008: Design and synthesis of 2-amino-isoxazolopyridines as Polo-like kinase inhibitors. Bioorganic and Medicinal Chemistry Letters 18(19): 5186-5189
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Annadurai, S.; Martinez, R.; Canney, D.J.; Eidem, T.; Dunman, P.M.; Abou-Gharbia, M. 2012: Design and synthesis of 2-aminothiazole based antimicrobials targeting MRSA. Bioorganic and Medicinal Chemistry Letters 22(24): 7719-7725
Keurulainen, L.; Salin, O.; Siiskonen, A.; Kern, J.M.; Alvesalo, J.; Kiuru, P.; Maass, M.; Yli-Kauhaluoma, J.; Vuorela, P. 2010: Design and synthesis of 2-arylbenzimidazoles and evaluation of their inhibitory effect against Chlamydia pneumoniae. Journal of Medicinal Chemistry 53(21): 7664-7674
La Regina, G.; Bai, R.; Rensen, W.; Coluccia, A.; Piscitelli, F.; Gatti, V.; Bolognesi, A.; Lavecchia, A.; Granata, I.; Porta, A.; Maresca, B.; Soriani, A.; Iannitto, M.L.; Mariani, M.; Santoni, A.; Brancale, A.; Ferlini, C.; Dondio, G.; Varasi, M.; Mercurio, C.; Hamel, E.; Lavia, P.; Novellino, E.; Silvestri, R. 2011: Design and synthesis of 2-heterocyclyl-3-arylthio-1H-indoles as potent tubulin polymerization and cell growth inhibitors with improved metabolic stability. Journal of Medicinal Chemistry 54(24): 8394-8406
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Moradi, A.; Navidpour, L.; Amini, M.; Sadeghian, H.; Shadnia, H.; Firouzi, O.; Miri, R.; Ebrahimi, S.E.S.; Abdollahi, M.; Zahmatkesh, M.H.; Shafiee, A. 2010: Design and synthesis of 2-phenoxynicotinic acid hydrazides as anti-inflammatory and analgesic agents. Archiv der Pharmazie 343(9): 509-518
Fuse, S.; Inaba, K.; Takagi, M.; Tanaka, M.; Hirokawa, T.; Johmoto, K.; Uekusa, H.; Shin-Ya, K.; Takahashi, T.; Doi, T. 2013: Design and synthesis of 2-phenyl-1,4-dioxa-spiro[4.5]deca-6,9-dien-8-ones as potential anticancer agents starting from cytotoxic spiromamakone a. European Journal of Medicinal Chemistry 66: 180-184
El Kazzouli, S.ïd.; Griffon du Bellay, A.; Berteina-Raboin, S.; Delagrange, P.; Caignard, D.-H.; Guillaumet, G.ér. 2011: Design and synthesis of 2-phenylimidazo[1,2-a]pyridines as a novel class of melatonin receptor ligands. European Journal of Medicinal Chemistry 46(9): 4252-4257
Chen, W.; Shen, Y.; Li, Z.; Zhang, M.; Lu, C.; Shen, Y. 2014: Design and synthesis of 2-phenylnaphthalenoids as inhibitors of DNA topoisomeraseIIα and antitumor agents. European Journal of Medicinal Chemistry 86: 782-796
Duan, Y.-T.; Wang, Z.-C.; Sang, Y.-L.; Tao, X.-X.; Teraiya, S.B.; Wang, P.-F.; Wen, Q.; Zhou, X.-J.; Ding, L.; Yang, Y.-H.; Zhu, H.-L. 2014: Design and synthesis of 2-styryl of 5-Nitroimidazole derivatives and antimicrobial activities as FabH inhibitors. European Journal of Medicinal Chemistry 76: 387-396
Chandrasekharappa, A.P.; Badiger, S.E.; Dubey, P.K.; Panigrahi, S.K.; Manukonda, S.R.V.V.V. 2013: Design and synthesis of 2-substituted benzoxazoles as novel PTP1B inhibitors. Bioorganic and Medicinal Chemistry Letters 23(9): 2579-2584
Matsuo, M.; Hasegawa, A.; Takano, M.; Saito, H.; Kakuda, S.; Takagi, K.; Ochiai, E.; Horie, K.; Takimoto-Kamimura, M.; Takenouchi, K.; Sawada, D.; Kittaka, A. 2014: Design and synthesis of 2α-(tetrazolylethyl)-1α,25-dihydroxyvitamin D3 as a high affinity ligand for vitamin D receptor. Journal of Steroid Biochemistry and Molecular Biology 144 Pt A: 201-203
Choi, M.-H.; Lee, C.-K.; Kim, H.-D. 2010: Design and synthesis of 3'-fluoropenciclovir analogues as antiviral agents. Archives of Pharmacal Research 33(2): 197-202
Shi, L.-H.; Jin, D.-Z.; Zhou, W.-C.; Wang, J.; Chen, X.-H. 2009: Design and synthesis of 3'-methyl-furanonucleosides and their anti-tumor activities. Yao Xue Xue Bao 44(7): 747-753
Xu, J.; Ai, J.; Liu, S.; Peng, X.; Yu, L.; Geng, M.; Nan, F. 2014: Design and synthesis of 3,3'-biscoumarin-based c-Met inhibitors. Organic and Biomolecular Chemistry 12(22): 3721-3734
Choi, M.; Hwang, Y.-S.; Kumar, A.S.; Jo, H.; Jeong, Y.; Oh, Y.; Lee, J.; Yun, J.; Kim, Y.; Han, S.-B.; Jung, J.-K.; Cho, J.; Lee, H. 2014: Design and synthesis of 3,4-dihydro-2H-benzo[h]chromene derivatives as potential NF-κB inhibitors. Bioorganic and Medicinal Chemistry Letters 24(11): 2404-2407
Zhou, Z.; Zhuo, J.; Yan, S.; Ma, L. 2013: Design and synthesis of 3,5-diaryl-4,5-dihydro-1H-pyrazoles as new tyrosinase inhibitors. Bioorganic and Medicinal Chemistry 21(7): 2156-2162
Kumar, A.; Maurya, R.Awatar.; Sharma, S.; Ahmad, P.; Singh, A.B.; Tamrakar, A.K.; Srivastava, A.K. 2009: Design and synthesis of 3,5-diarylisoxazole derivatives as novel class of anti-hyperglycemic and lipid lowering agents. Bioorganic and Medicinal Chemistry 17(14): 5285-5292
Babu, M.; Pitchumani, K.; Ramesh, P. 2012: Design and synthesis of 3,5-diarylpiperidin-2,6-diones as anticonvulsant agents. Bioorganic and Medicinal Chemistry Letters 22(2): 1263-1266
Das, B.C.; Tang, X.-Y.; Rogler, P.; Evans, T. 2012: Design and synthesis of 3,5-disubstituted boron-containing 1,2,4-oxadiazoles as potential combretastatin A-4 (CA-4) analogs. Tetrahedron Letters 53(31): 3947-3950
Kumar, D.; Patel, G.; Vijayakrishnan, L.; Dastidar, S.G.; Ray, A. 2012: Design and synthesis of 3,5-disubstituted-1,2,4-oxadiazoles as potent inhibitors of phosphodiesterase4b2. Chemical Biology and Drug Design 79(5): 810-818
Han, S.-Y.; Choi, J.W.; Yang, J.; Chae, C.H.; Lee, J.; Jung, H.; Lee, K.; Ha, J.D.; Kim, H.R.; Cho, S.Y. 2012: Design and synthesis of 3-(4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridin-2-yl)-1H-quinolin-2-ones as VEGFR-2 kinase inhibitors. Bioorganic and Medicinal Chemistry Letters 22(8): 2837-2842
Alagarsamy, V.; Raja Solomon, V.; Murugan, M.; Dhanabal, K.; Parthiban, P.; Anjana, G.V. 2008: Design and synthesis of 3-(4-ethylphenyl)-2-substituted amino-3H-quinazolin-4-ones as a novel class of analgesic and anti-inflammatory agents. Journal of Enzyme Inhibition and Medicinal Chemistry 23(6): 839-847
Kumar, L.; Sarswat, A.; Lal, N.; Jain, A.; Kumar, S.; Kiran Kumar, S.T.V.S.; Maikhuri, J.P.; Pandey, A.K.; Shukla, P.K.; Gupta, G.; Sharma, V.L. 2011: Design and synthesis of 3-(azol-1-yl)phenylpropanes as microbicidal spermicides for prophylactic contraception. Bioorganic and Medicinal Chemistry Letters 21(1): 176-181
Solomon, V.R.; Haq, W.; Srivastava, K.; Puri, S.K.; Katti, S.B. 2013: Design and synthesis of 3-[(7-chloro-1-oxidoquinolin-4-ylamino)alkyl]-1,3-thiazolidin-4-ones as antimalarial agents. Journal of Enzyme Inhibition and Medicinal Chemistry 28(5): 1048-1053
Zebardast, T.; Zarghi, A.; Daraie, B.; Hedayati, M.; Dadrass, O.G. 2009: Design and synthesis of 3-alkyl-2-aryl-1,3-thiazinan-4-one derivatives as selective cyclooxygenase (COX-2) inhibitors. Bioorganic and Medicinal Chemistry Letters 19(12): 3162-3165
Aiello, F.; Shabaik, Y.; Esqueda, A.; Sanchez, T.W.; Grande, F.; Garofalo, A.; Neamati, N. 2012: Design and synthesis of 3-carbamoylbenzoic acid derivatives as inhibitors of human apurinic/apyrimidinic endonuclease 1 (APE1). Chemmedchem 7(10): 1825-1839
Abdelsayed, S.; Ha Duong, N.T.; Hai, J.; Hémadi, M.; El Hage Chahine, J.M.; Verbeke, P.; Serradji, N. 2014: Design and synthesis of 3-isoxazolidone derivatives as new Chlamydia trachomatis inhibitors. Bioorganic and Medicinal Chemistry Letters 24(16): 3854-3860
Hafez, H.N.; El-Gazzar, A.B.A. 2008: Design and synthesis of 3-pyrazolyl-thiophene, thieno[2,3-d]pyrimidines as new bioactive and pharmacological activities. Bioorganic and Medicinal Chemistry Letters 18(19): 5222-5227
Miyamoto, Y.; Banno, Y.; Yamashita, T.; Fujimoto, T.; Oi, S.; Moritoh, Y.; Asakawa, T.; Kataoka, O.; Takeuchi, K.; Suzuki, N.; Ikedo, K.; Kosaka, T.; Tsubotani, S.; Tani, A.; Funami, M.; Amano, M.; Yamamoto, Y.; Aertgeerts, K.; Yano, J.; Maezaki, H. 2011: Design and synthesis of 3-pyridylacetamide derivatives as dipeptidyl peptidase IV (DPP-4) inhibitors targeting a bidentate interaction with Arg125. Bioorganic and Medicinal Chemistry 19(1): 172-185
Hess, M.; Schulze Elfringhoff, A.; Lehr, M. 2008: Design and synthesis of 3-pyrrol-3-yl-3H-isobenzofuran-1-ones as inhibitors of human cytosolic phospholipase A2alpha. Journal of Enzyme Inhibition and Medicinal Chemistry 23(6): 946-957
Wei, Y.; Zhao, Z.; Liu, J.; Xu, C.; Jiang, G.; Duan, A. 2013: Design and synthesis of 3D ordered macroporous CeO₂-supported Pt@CeO(2-δ) core-shell nanoparticle materials for enhanced catalytic activity of soot oxidation. Small 9(23): 3957-3963
Duivenvoorden, B.A.; Ghauharali, K.; Scheij, S.; Boot, R.G.; Aerts, J.M.F.G.; van der Marel, G.A.; Overkleeft, H.S.; Codée, J.D.C. 2014: Design and synthesis of 4'-O-alkyl-chitobiosyl-4-methylumbelliferone as human chitinase fluorogenic substrates. Carbohydrate Research 399: 26-37
Li, H.-Q.; Li, D.-D.; Lu, X.; Xu, Y.-Y.; Zhu, H.-L. 2012: Design and synthesis of 4,6-substituted-(diaphenylamino)quinazolines as potent EGFR inhibitors with antitumor activity. Bioorganic and Medicinal Chemistry 20(1): 317-323
Zhu, L.; Li, Y.; Qiu, L.; Su, M.; Wang, X.; Xia, C.; Qu, Y.; Li, J.; Li, J.; Xiong, B.; Shen, J. 2013: Design and synthesis of 4-(2,4,5-trifluorophenyl)butane-1,3-diamines as dipeptidyl peptidase IV inhibitors. Chemmedchem 8(7): 1104-1116
Lee, B.; Kwak, J.-H.; Huang, S.-W.; Jang, J.-Y.; Lim, S.; Kwak, Y.-S.; Lee, K.; Kim, H.S.; Han, S.-B.; Hong, J.-T.; Lee, H.; Song, S.; Seo, S.-Y.; Jung, J.-K. 2012: Design and synthesis of 4-O-methylhonokiol analogs as inhibitors of cyclooxygenase-2 (COX-2) and PGF₁ production. Bioorganic and Medicinal Chemistry 20(9): 2860-2868
Xiao, H.-Y.; Balog, A.; Attar, R.M.; Fairfax, D.; Fleming, L.B.; Holst, C.L.; Martin, G.S.; Rossiter, L.M.; Chen, J.; Cvjic, M.-E.; Dell-John, J.; Geng, J.; Gottardis, M.M.; Han, W.-C.; Nation, A.; Obermeier, M.; Rizzo, C.A.; Schweizer, L.; Spires, T.; Shan, W.; Gavai, A.; Salvati, M.E.; Vite, G. 2010: Design and synthesis of 4-[3,5-dioxo-11-oxa-4,9-diazatricyclo[5.3.1.0(2,6)]undec-4-yl]-2-trifluoromethyl-benzonitriles as androgen receptor antagonists. Bioorganic and Medicinal Chemistry Letters 20(15): 4491-4495
Li, W.; Xia, L.; Hu, A.; Liu, A.; Peng, J.; Tan, W. 2013: Design and synthesis of 4-alkyl-2-amino(acetamino)-6-aryl-1,3-thiazine derivatives as influenza neuraminidase inhibitors. Archiv der Pharmazie 346(9): 635-644
Gorja, D.R.; Shiva Kumar, K.; Kandale, A.; Meda, C.L.T.; Parsa, K.V.L.; Mukkanti, K.; Pal, M. 2012: Design and synthesis of 4-alkynyl pyrazoles as inhibitors of PDE4: a practical access via Pd/C-Cu catalysis. Bioorganic and Medicinal Chemistry Letters 22(7): 2480-2487
Le, T.N.; Yang, S.H.; Khadka, D.B.; Van, H.T.M.; Cho, S.H.; Kwon, Y.; Lee, E.-S.; Lee, K.-T.; Cho, W.-J. 2011: Design and synthesis of 4-amino-2-phenylquinazolines as novel topoisomerase i inhibitors with molecular modeling. Bioorganic and Medicinal Chemistry 19(14): 4399-4404
Zhang, Y.; Jung, S.Y.; Jin, C.; Kim, N.D.; Gong, P.; Lee, Y.S. 2009: Design and synthesis of 4-aryl-4-oxobutanoic acid amides as calpain inhibitors. Bioorganic and Medicinal Chemistry Letters 19(2): 502-507
Li, G.; Zhou, H.; Jiang, Y.; Keim, H.; Topiol, S.W.; Poda, S.B.; Ren, Y.; Chandrasena, G.; Doller, D.ío. 2011: Design and synthesis of 4-arylpiperidinyl amide and N-arylpiperdin-3-yl-cyclopropane carboxamide derivatives as novel melatonin receptor ligands. Bioorganic and Medicinal Chemistry Letters 21(4): 1236-1242
Liu, S.; Zha, C.; Nacro, K.; Hu, M.; Cui, W.; Yang, Y.-L.; Bhatt, U.; Sambandam, A.; Isherwood, M.; Yet, L.; Herr, M.T.; Ebeltoft, S.; Hassler, C.; Fleming, L.; Pechulis, A.D.; Payen-Fornicola, A.; Holman, N.; Milanowski, D.; Cotterill, I.; Mozhaev, V.; Khmelnitsky, Y.; Guzzo, P.R.; Sargent, B.J.; Molino, B.F.; Olson, R.; King, D.; Lelas, S.; Li, Y.-W.; Johnson, K.; Molski, T.; Orie, A.; Ng, A.; Haskell, R.; Clarke, W.; Bertekap, R.; O'Connell, J.; Lodge, N.; Sinz, M.; Adams, S.; Zaczek, R.; Macor, J.E. 2014: Design and synthesis of 4-heteroaryl 1,2,3,4-tetrahydroisoquinolines as triple reuptake inhibitors. Acs Medicinal Chemistry Letters 5(7): 760-765
Malamas, M.S.; Erdei, J.; Gunawan, I.; Turner, J.; Hu, Y.; Wagner, E.; Fan, K.; Chopra, R.; Olland, A.; Bard, J.; Jacobsen, S.; Magolda, R.L.; Pangalos, M.; Robichaud, A.J. 2010: Design and synthesis of 5,5'-disubstituted aminohydantoins as potent and selective human beta-secretase (BACE1) inhibitors. Journal of Medicinal Chemistry 53(3): 1146-1158
Ramurthy, S.; Aikawa, M.; Amiri, P.; Costales, A.; Hashash, A.; Jansen, J.M.; Lin, S.; Ma, S.; Renhowe, P.A.; Shafer, C.M.; Subramanian, S.; Sung, L.; Verhagen, J. 2011: Design and synthesis of 5,6-fused heterocyclic amides as Raf kinase inhibitors. Bioorganic and Medicinal Chemistry Letters 21(11): 3286-3289
Ha, Y.M.; Park, Y.J.; Kim, J.-A.; Park, D.; Park, J.Y.; Lee, H.J.; Lee, J.Y.; Moon, H.R.; Chung, H.Y. 2012: Design and synthesis of 5-(substituted benzylidene)thiazolidine-2,4-dione derivatives as novel tyrosinase inhibitors. European Journal of Medicinal Chemistry 49: 245-252
Hasumi, K.; Sato, S.; Saito, T.; Kato, J.-y.; Shirota, K.; Sato, J.; Suzuki, H.; Ohta, S. 2014: Design and synthesis of 5-[(2-chloro-6-fluorophenyl)acetylamino]-3-(4-fluorophenyl)-4-(4-pyrimidinyl)isoxazole (AKP-001), a novel inhibitor of p38 MAP kinase with reduced side effects based on the antedrug concept. Bioorganic and Medicinal Chemistry 22(15): 4162-4176
Guo, L.-J.; Wei, C.-X.; Jia, J.-H.; Zhao, L.-M.; Quan, Z.-S. 2009: Design and synthesis of 5-alkoxy-[1,2,4]triazolo[4,3-a]quinoline derivatives with anticonvulsant activity. European Journal of Medicinal Chemistry 44(3): 954-958
Ramurthy, S.; Costales, A.; Jansen, J.M.; Levine, B.; Renhowe, P.A.; Shafer, C.M.; Subramanian, S. 2012: Design and synthesis of 6,6-fused heterocyclic amides as raf kinase inhibitors. Bioorganic and Medicinal Chemistry Letters 22(4): 1678-1681
Yadav, M.R.; Naik, P.P.; Gandhi, H.P.; Chauhan, B.S.; Giridhar, R. 2013: Design and synthesis of 6,7-dimethoxyquinazoline analogs as multi-targeted ligands for α1- and AII-receptors antagonism. Bioorganic and Medicinal Chemistry Letters 23(13): 3959-3966
Chen, Y.-F.; Lin, Y.-C.; Huang, P.-K.; Chan, H.-C.; Kuo, S.-C.; Lee, K.-H.; Huang, L.-J. 2013: Design and synthesis of 6,7-methylenedioxy-4-substituted phenylquinolin-2(1H)-one derivatives as novel anticancer agents that induce apoptosis with cell cycle arrest at G2/M phase. Bioorganic and Medicinal Chemistry 21(17): 5064-5075
Sato, I.; Morihira, K.; Inami, H.; Kubota, H.; Morokata, T.; Suzuki, K.; Iura, Y.; Nitta, A.; Imaoka, T.; Takahashi, T.; Takeuchi, M.; Ohta, M.; Tsukamoto, S.-I. 2008: Design and synthesis of 6-fluoro-2-naphthyl derivatives as novel CCR3 antagonists with reduced CYP2D6 inhibition. Bioorganic and Medicinal Chemistry 16(18): 8607-8618
Lou, J.; Yang, X.; Rao, Z.; Qi, W.; Li, J.; Wang, H.; Li, Y.; Li, J.; Wang, Z.; Hu, X.; Liu, P.; Hong, X. 2014: Design and synthesis of 6-oxo-1,4,5,6-tetrahydropyrimidine-5-carboxylate derivatives as neuraminidase inhibitors. European Journal of Medicinal Chemistry 83: 466-473
Kaller, M.R.; Zhong, W.; Henley, C.; Magal, E.; Nguyen, T.; Powers, D.; Rzasa, R.M.; Wang, W.; Xiong, X.; Norman, M.H. 2009: Design and synthesis of 6-oxo-1,6-dihydropyridines as CDK5 inhibitors. Bioorganic and Medicinal Chemistry Letters 19(23): 6591-6594
Westaway, S.M.; Thompson, M.; Rami, H.K.; Stemp, G.; Trouw, L.S.; Mitchell, D.J.; Seal, J.T.; Medhurst, S.J.; Lappin, S.C.; Biggs, J.; Wright, J.; Arpino, S.; Jerman, J.C.; Cryan, J.E.; Holland, V.; Winborn, K.Y.; Coleman, T.; Stevens, A.J.; Davis, J.B.; Gunthorpe, M.J. 2008: Design and synthesis of 6-phenylnicotinamide derivatives as antagonists of TRPV1. Bioorganic and Medicinal Chemistry Letters 18(20): 5609-5613
Han, Q.; Li, Q.-J.; He, J.; Hu, B.; Tan, H.; Abliz, Z.; Wang, C.-H.; Yu, Y.; Yang, H.-B. 2011: Design and synthesis of 60° dendritic donor ligands and their coordination-driven self-assembly into supramolecular rhomboidal metallodendrimers. Journal of Organic Chemistry 76(23): 9660-9669
Shin, D.; Lee, S-Chul.; Heo, Y-Seok.; Lee, W-Young.; Cho, Y-Soon.; Kim, Y.Eun.; Hyun, Y-Lan.; Cho, J.Myung.; Lee, Y.Sup.; Ro, S. 2007: Design and synthesis of 7-hydroxy-1H-benzoimidazole derivatives as novel inhibitors of glycogen synthase kinase-3beta. Bioorganic and Medicinal Chemistry Letters 17(20): 5686-5689
Ariyasu, S.; Sawa, A.; Morita, A.; Hanaya, K.; Hoshi, M.; Takahashi, I.; Wang, B.; Aoki, S. 2014: Design and synthesis of 8-hydroxyquinoline-based radioprotective agents. Bioorganic and Medicinal Chemistry 22(15): 3891-3905
Song, B.; Xiao, T.; Qi, X.; Li, L.-N.; Qin, K.; Nian, S.; Hu, G.-X.; Yu, Y.; Liang, G.; Ye, F. 2012: Design and synthesis of 8-substituted benzamido-phenylxanthine derivatives as MAO-B inhibitors. Bioorganic and Medicinal Chemistry Letters 22(4): 1739-1742
Altiparmak, B.; Lambrecht, F.Y.; Bayrak, E.; Durkan, K. 2010: Design and synthesis of 99mTc-citro-folate for use as a tumor-targeted radiopharmaceutical. International Journal of Pharmaceutics 400(1-2): 8-14
Hu, Y.; Li, X.; Sebti, S.M.; Chen, J.; Cai, J. 2011: Design and synthesis of AApeptides: a new class of peptide mimics. Bioorganic and Medicinal Chemistry Letters 21(5): 1469-1471
Wolters, J.C.; Roelfes, G.; Poolman, B. 2011: Design and synthesis of ATP-based nucleotide analogues and profiling of nucleotide-binding proteins. Bioconjugate Chemistry 22(7): 1345-1353
Liu, Y.; Wu, J.; Weissig, H.; Betancort, J.M.; Gai, W.Z.; Leventhal, P.S.; Patricelli, M.P.; Samii, B.; Szardenings, A.K.; Shreder, K.R.; Kozarich, J.W. 2008: Design and synthesis of AX4697, a bisindolylmaleimide exo-affinity probe that labels protein kinase C alpha and beta. Bioorganic and Medicinal Chemistry Letters 18(22): 5955-5958
Wångsell, F.; Russo, F.; Sävmarker, J.; Rosenquist, A.; Samuelsson, B.; Larhed, M. 2009: Design and synthesis of BACE-1 inhibitors utilizing a tertiary hydroxyl motif as the transition state mimic. Bioorganic and Medicinal Chemistry Letters 19(16): 4711-4714
Chorell, E.; Pinkner, J.S.; Phan, G.; Edvinsson, S.; Buelens, F.; Remaut, H.; Waksman, G.; Hultgren, S.J.; Almqvist, F. 2010: Design and synthesis of C-2 substituted thiazolo and dihydrothiazolo ring-fused 2-pyridones: pilicides with increased antivirulence activity. Journal of Medicinal Chemistry 53(15): 5690-5695
Singh, P.; Faridi, U.; Srivastava, S.; Kumar, J.K.; Darokar, M.P.; Luqman, S.; Shanker, K.; Chanotiya, C.S.; Gupta, A.; Gupta, M.M.; Negi, A.S. 2010: Design and synthesis of C-ring lactone- and lactam-based podophyllotoxin analogues as anticancer agents. Chemical and Pharmaceutical Bulletin 58(2): 242-246
Wang, L.; Gagey-Eilstein, N.; Broussy, S.; Reille-Seroussi, M.; Huguenot, F.; Vidal, M.; Liu, W.-Q. 2014: Design and synthesis of C-terminal modified cyclic peptides as VEGFR1 antagonists. Molecules 19(10): 15391-15407
Albright, A.; Eddings, D.; Black, R.; Welch, C.J.; Gerasimchuk, N.N.; Gawley, R.E. 2011: Design and synthesis of C2-symmetric N-heterocyclic carbene precursors and metal carbenoids. Journal of Organic Chemistry 76(18): 7341-7351
Kamal, A.; Srinivasulu, V.; Nayak, V.L.; Sathish, M.; Shankaraiah, N.; Bagul, C.; Reddy, N.V.S.; Rangaraj, N.; Nagesh, N. 2014: Design and synthesis of C3-pyrazole/chalcone-linked beta-carboline hybrids: antitopoisomerase I, DNA-interactive, and apoptosis-inducing anticancer agents. Chemmedchem 9(9): 2084-2098
Kojima, N.; Suga, Y.; Hayashi, H.; Yamori, T.; Yoshimitsu, T.; Tanaka, T. 2011: Design and synthesis of C35-fluorinated solamins and their growth inhibitory activities against human cancer cell lines. Bioorganic and Medicinal Chemistry Letters 21(19): 5745-5749
Hoque, M.A.; Islam, M.N.; Islam, M.S.; Kato, T.; Nishino, N.; Ito, A.; Yoshida, M. 2014: Design and synthesis of CHAP31, trapoxin B and HC-toxin based bicyclic tetrapeptides disulfide as potent histone deacetylase inhibitors. Bioorganic and Medicinal Chemistry 22(15): 3850-3855
Makowska, M.łg.; Łukowska-Chojnacka, E.; Wińska, P.; Kuś, A.; Bilińska-Chomik, A.; Bretner, M. 2011: Design and synthesis of CK2 inhibitors. Molecular and Cellular Biochemistry 356(1-2): 91-96
Banday, A.H.; Giri, A.K.; Parveen, R.; Bashir, N. 2014: Design and synthesis of D-ring steroidal isoxazolines and oxazolines as potential antiproliferative agents against LNCaP, PC-3 and DU-145 cells. Steroids 87: 93-98
Rangnekar, A.; Gothelf, K.V.; LaBean, T.H. 2011: Design and synthesis of DNA four-helix bundles. Nanotechnology 22(23): 235601
Giovanni, A.; Roehr, J.; Dwyer, S.; Neuenschwander, K.; Scotese, A.; Moorcroft, N.D.; Davis, L.; Gao, Z. 2013: Design and synthesis of D₁ agonist/D₂ antagonist for treatment of schizophrenia. Bioorganic and Medicinal Chemistry Letters 23(5): 1498-1501
Petch, D.; Anderson, R.J.; Cunningham, A.; George, S.E.; Hibbs, D.E.; Liu, R.; Mackay, S.P.; Paul, A.; Small, D.A.P.; Groundwater, P.W. 2012: Design and synthesis of EGFR dimerization inhibitors and evaluation of their potential in the treatment of psoriasis. Bioorganic and Medicinal Chemistry 20(19): 5901-5914
Chen, J.; Zhang, P.; Fang, G.; Yi, P.; Zeng, F.; Wu, S. 2012: Design and synthesis of FRET-mediated multicolor and photoswitchable fluorescent polymer nanoparticles with tunable emission properties. Journal of Physical Chemistry. B 116(14): 4354-4362
Qian, W.-J.; Lai, C.C.; Kelley, J.A.; Burke, T.R. 2014: Design and synthesis of Fmoc-Thr[PO(OH)(OPOM)] for the preparation of peptide prodrugs containing phosphothreonine in fully protected form. Chemistry and Biodiversity 11(5): 784-791
Zhu, T.; Fawzi, M.B.; Flint, M.; Kong, F.; Szeliga, J.; Tsao, R.; Howe, A.Y.M.; Pan, W. 2010: Design and synthesis of HCV agents with sequential triple inhibitory potentials. Bioorganic and Medicinal Chemistry Letters 20(17): 5212-5216
Kesteleyn, B.; Amssoms, K.; Schepens, W.; Hache, G.; Verschueren, W.; Van De Vreken, W.; Rombauts, K.; Meurs, G.; Sterkens, P.; Stoops, B.; Baert, L.; Austin, N.; Wegner, J.ör.; Masungi, C.; Dierynck, I.; Lundgren, S.; Jönsson, D.; Parkes, K.; Kalayanov, G.; Wallberg, H.; Rosenquist, A.; Samuelsson, B.; Van Emelen, K.; Thuring, J.W. 2013: Design and synthesis of HIV-1 protease inhibitors for a long-acting injectable drug application. Bioorganic and Medicinal Chemistry Letters 23(1): 310-317
Sellers, R.P.; Alexander, L.D.; Johnson, V.A.; Lin, C.-C.; Savage, J.; Corral, R.; Moss, J.; Slugocki, T.S.; Singh, E.K.; Davis, M.R.; Ravula, S.; Spicer, J.E.; Oelrich, J.L.; Thornquist, A.; Pan, C.-M.; McAlpine, S.R. 2010: Design and synthesis of Hsp90 inhibitors: exploring the SAR of Sansalvamide a derivatives. Bioorganic and Medicinal Chemistry 18(18): 6822-6856
Suzuki, Y.; Yokoyama, K. 2008: Design and synthesis of ICT-based fluorescent probe for high-sensitivity protein detection and application to rapid protein staining for SDS-PAGE. Proteomics 8(14): 2785-2790
Nagase, H.; Nemoto, T.; Matsubara, A.; Saito, M.; Yamamoto, N.; Osa, Y.; Hirayama, S.; Nakajima, M.; Nakao, K.; Mochizuki, H.; Fujii, H. 2010: Design and synthesis of KNT-127, a δ-opioid receptor agonist effective by systemic administration. Bioorganic and Medicinal Chemistry Letters 20(21): 6302-6305
Patel, B.A.; Krishnan, R.; Khadtare, N.; Gurukumar, K.R.; Basu, A.; Arora, P.; Bhatt, A.; Patel, M.R.; Dana, D.; Kumar, S.; Kaushik-Basu, N.; Talele, T.T. 2013: Design and synthesis of L- and D-phenylalanine derived rhodanines with novel C5-arylidenes as inhibitors of HCV NS5B polymerase. Bioorganic and Medicinal Chemistry 21(11): 3262-3271
Sharma, V.K.; Singh, S.K.; Bohra, K.; L, C.Shekhar.Reddy.; Khatri, V.; Olsen, C.E.; Prasad, A.K. 2013: Design and synthesis of LNA-based mercaptoacetamido-linked nucleoside dimers. Nucleosides Nucleotides and Nucleic Acids 32(5): 256-272
Lyu, A.; Fang, L.; Gou, S. 2014: Design and synthesis of Lapatinib derivatives containing a branched side chain as HER1/HER2 targeting antitumor drug candidates. European Journal of Medicinal Chemistry 87: 631-642
Freskos, J.N.; Asmelash, B.; Gaston, K.R.; Karwa, A.; Marzan, T.A.; Nickols, M.A.; Rogers, T.E.; Schoenstein, T.; Sympson, C.J.; Vu, B. 2013: Design and synthesis of MMP inhibitors with appended fluorescent tags for imaging and visualization of matrix metalloproteinase enzymes. Bioorganic and Medicinal Chemistry Letters 23(20): 5566-5570
Li, Q.; Wang, Z.-L.; Li, G.-R.; Guo, R.; Ding, L.-X.; Tong, Y.-X. 2012: Design and synthesis of MnO₂/Mn/MnO₂ sandwich-structured nanotube arrays with high supercapacitive performance for electrochemical energy storage. Nano Letters 12(7): 3803-3807
Choi, W.J.; Lee, H.W.; Kim, H.O.; Chinn, M.; Gao, Z.-G.; Patel, A.; Jacobson, K.A.; Moon, H.R.; Jung, Y.H.; Jeong, L.S. 2009: Design and synthesis of N(6)-substituted-4'-thioadenosine-5'-uronamides as potent and selective human A(3) adenosine receptor agonists. Bioorganic and Medicinal Chemistry 17(23): 8003-8011
Alexiou, P.; Nicolaou, I.; Stefek, M.; Kristl, A.; Demopoulos, V.J. 2008: Design and synthesis of N-(3,5-difluoro-4-hydroxyphenyl)benzenesulfonamides as aldose reductase inhibitors. Bioorganic and Medicinal Chemistry 16(7): 3926-3932
Chen, C.-N.; Lv, L.-L.; Ji, F.-Q.; Chen, Q.; Xu, H.; Niu, C.-W.; Xi, Z.; Yang, G.-F. 2009: Design and synthesis of N-2,6-difluorophenyl-5-methoxyl-1,2,4-triazolo[1,5-a]-pyrimidine-2-sulfonamide as acetohydroxyacid synthase inhibitor. Bioorganic and Medicinal Chemistry 17(8): 3011-3017
Barcelos, R.C.; Pastre, J.C.; Vendramini-Costa, D.éb.B.; Caixeta, V.; Longato, G.B.; Monteiro, P.A.új.; de Carvalho, J.ão.E.; Pilli, R.A. 2014: Design and synthesis of N-acylated aza-goniothalamin derivatives and evaluation of their in vitro and in vivo antitumor activity. Chemmedchem 9(12): 2725-2743
Liu, X.; Zhang, L.; Tan, J.-G.; Xu, H.-H. 2013: Design and synthesis of N-alkyl-N'-substituted 2,4-dioxo-3,4-dihydropyrimidin-1-diacylhydrazine derivatives as ecdysone receptor agonist. Bioorganic and Medicinal Chemistry 21(15): 4687-4697
Du, Y.; Ye, H.; Guo, F.; Wang, L.; Gill, T.; Khan, N.; Cuconati, A.; Guo, J.-T.; Block, T.M.; Chang, J.; Xu, X. 2013: Design and synthesis of N-alkyldeoxynojirimycin derivatives with improved metabolic stability as inhibitors of BVDV and Tacaribe virus. Bioorganic and Medicinal Chemistry Letters 23(14): 4258-4262
Ma, C.; Wu, A.; Wu, Y.; Ren, X.; Cheng, M. 2013: Design and synthesis of N-aryl isothioureas as a novel class of gastric H(+) /K(+) -ATPase inhibitors. Archiv der Pharmazie 346(12): 891-900
Liu, X.-H.; Ruan, B.-F.; Liu, J.-X.; Song, B.-A.; Jing, L.-H.; Li, J.; Yang, Y.; Zhu, H.-L.; Qi, X.-B. 2011: Design and synthesis of N-phenylacetyl (sulfonyl) 4,5-dihydropyrazole derivatives as potential antitumor agents. Bioorganic and Medicinal Chemistry Letters 21(10): 2916-2920
Patel, M.R.; Pandya, K.G.; Lau-Cam, C.A.; Singh, S.; Pino, M.A.; Billack, B.; Degenhardt, K.; Talele, T.T. 2012: Design and synthesis of N-substituted indazole-3-carboxamides as poly(ADP-ribose)polymerase-1 (PARP-1) inhibitors(†). Chemical Biology and Drug Design 79(4): 488-496
Soltan, M.K.; Ghonaim, H.M.; El Sadek, M.; Kull, M.A.; El-aziz, L.A.; Blagbrough, I.S. 2009: Design and synthesis of N4,N9-disubstituted spermines for non-viral siRNA delivery--structure-activity relationship studies of si Fection efficiency versus toxicity. Pharmaceutical Research 26(2): 286-295
Kode, N.R.; Vanden Eynde, J.J.; Mayence, A.; Wang, G.; Huang, T.L. 2013: Design and synthesis of N¹,N⁵-bis[4-(5-alkyl-1,2,4-oxadiazol-3-yl)phenyl]glutaramides as potential antifungal prodrugs. Molecules 18(9): 11250-11263
Monforte, A.-M.; Ferro, S.; De Luca, L.; Lo Surdo, G.; Morreale, F.; Pannecouque, C.; Balzarini, J.; Chimirri, A. 2014: Design and synthesis of N₁-aryl-benzimidazoles 2-substituted as novel HIV-1 non-nucleoside reverse transcriptase inhibitors. Bioorganic and Medicinal Chemistry 22(4): 1459-1467
Li, T.; Guo, L.; Zhang, Y.; Wang, J.; Li, Z.; Lin, L.; Zhang, Z.; Li, L.; Lin, J.; Zhao, W.; Li, J.; Wang, P.G. 2011: Design and synthesis of O-GlcNAcase inhibitors via 'click chemistry' and biological evaluations. Carbohydrate Research 346(9): 1083-1092
Joshi, A.; Véron, J.-B.; Unge, J.; Rosenquist, Ås.; Wallberg, H.; Samuelsson, B.; Hallberg, A.; Larhed, M. 2013: Design and synthesis of P1-P3 macrocyclic tertiary-alcohol-comprising HIV-1 protease inhibitors. Journal of Medicinal Chemistry 56(22): 8999-9007
Huang, H.; Wang, X. 2013: Design and synthesis of Pd-MnO2 nanolamella-graphene composite as a high-performance multifunctional electrocatalyst towards formic acid and methanol oxidation. Physical Chemistry Chemical Physics: Pccp 15(25): 10367-10375
Skouta, R.; Hayano, M.; Shimada, K.; Stockwell, B.R. 2012: Design and synthesis of Pictet-Spengler condensation products that exhibit oncogenic-RAS synthetic lethality and induce non-apoptotic cell death. Bioorganic and Medicinal Chemistry Letters 22(17): 5707-5713
Schütz, M.; Müller, C.I.; Salehi, M.; Lambert, C.; Schlücker, S. 2011: Design and synthesis of Raman reporter molecules for tissue imaging by immuno-SERS microscopy. Journal of Biophotonics 4(6): 453-463
Tao, H.; Weng, Y.; Zhuo, R.; Chang, G.; Urbatsch, I.L.; Zhang, Q. 2011: Design and synthesis of Selenazole-containing peptides for cocrystallization with P-glycoprotein. Chembiochem: a European Journal of Chemical Biology 12(6): 868-873
Papanastasiou, I.; Tsotinis, A.; Zoidis, G.; Kolocouris, N.; Prathalingam, S.R.; Kelly, J.M. 2009: Design and synthesis of Trypanosoma brucei active 1-alkyloxy and 1-benzyloxyadamantano 2-guanylhydrazones. Chemmedchem 4(7): 1059-1062
Bhaskar Reddy, M.; Shailaja, M.; Manjula, A.; Premkumar, J.R.; Sastry, G.N.; Sirisha, K.; Sarma, A.V.S. 2015: Design and synthesis of Tröger's base ditopic receptors: host-guest interactions, a combined theoretical and experimental study. Organic and Biomolecular Chemistry 13(4): 1141-1149
Werner, S.; Kasi, D.; Brummond, K.M. 2007: Design and synthesis of a 3,4-dehydroproline amide discovery library. Journal of Combinatorial Chemistry 9(4): 677-683
Fujii, T.; Shindo, Y.; Hotta, K.; Citterio, D.; Nishiyama, S.; Suzuki, K.; Oka, K. 2014: Design and synthesis of a FlAsH-type Mg2+ fluorescent probe for specific protein labeling. Journal of the American Chemical Society 136(6): 2374-2381
Roberge, J.Y.; Harikrishnan, L.S.; Kamau, M.G.; Ruan, Z.; Van Kirk, K.; Liu, Y.; Cooper, C.B.; Poss, M.A.; Dickson, J.K.; Gavai, A.V.; Chao, S.T.; Leith, L.W.; Bednarz, M.S.; Mathur, A.; Kakarla, R.; Schnur, D.M.; Vaz, R.; Lawrence, R.Michael. 2009: Design and synthesis of a G-protein-coupled receptor antagonist library of aryloxyalkanolamines using a polymer-supported acyclic acetal linker. Journal of Combinatorial Chemistry 11(1): 72-82
Fan, B.; Li, N. 2009: Design and synthesis of a Magainin2 fusion protein gene suitable for a mammalian expression system. Transgenic Research 18(1): 99-112
Phelan, R.M.; Ostermeier, M.; Townsend, C.A. 2009: Design and synthesis of a beta-lactamase activated 5-fluorouracil prodrug. Bioorganic and Medicinal Chemistry Letters 19(4): 1261-1263
Baker, Y.R.; Galloway, W.R.J.D.; Hodgkinson, J.T.; Spring, D.R. 2013: Design and synthesis of a biotinylated chemical probe for detecting the molecular targets of an inhibitor of the production of the Pseudomonas aeruginosa virulence factor pyocyanin. Molecules 18(10): 11783-11796
Zhong, B.; Lama, R.; Smith, K.M.; Xu, Y.; Su, B. 2011: Design and synthesis of a biotinylated probe of COX-2 inhibitor nimesulide analog JCC76. Bioorganic and Medicinal Chemistry Letters 21(18): 5324-5327
Yuan, Y.; Arnatt, C.K.; Li, G.; Haney, K.M.; Ding, D.; Jacob, J.C.; Selley, D.E.; Zhang, Y. 2012: Design and synthesis of a bivalent ligand to explore the putative heterodimerization of the mu opioid receptor and the chemokine receptor CCR5. Organic and Biomolecular Chemistry 10(13): 2633-2646
Kannan, R.; Pillarsetty, N.; Gali, H.; Hoffman, T.J.; Barnes, C.L.; Jurisson, S.S.; Smith, C.J.; Volkert, W.A. 2011: Design and synthesis of a bombesin peptide-conjugated tripodal phosphino dithioether ligand topology for the stabilization of the fac-[M(CO)3]+ core (M=(99 m)Tc or Re). Inorganic Chemistry 50(13): 6210-6219
Aoki, S.; Sakurama, K.; Ohshima, R.; Matsuo, N.; Yamada, Y.; Takasawa, R.; Tanuma, S.-i.; Takeda, K.; Kimura, E. 2008: Design and synthesis of a caged Zn2+ probe, 8-benzenesulfonyloxy-5-N,N-dimethylaminosulfonylquinolin-2-ylmethyl-pendant 1,4,7,10-tetraazacyclododecane, and its hydrolytic uncaging upon complexation with Zn2+. Inorganic Chemistry 47(7): 2747-2754
Srinivasrao, G.; Park, J.-E.; Kim, S.; Ahn, M.; Cheong, C.; Nam, K.-Y.; Gunasekaran, P.; Hwang, E.; Kim, N.-H.; Shin, S.Y.; Lee, K.S.; Ryu, E.; Bang, J.K. 2014: Design and synthesis of a cell-permeable, drug-like small molecule inhibitor targeting the polo-box domain of polo-like kinase 1. Plos one 9(9): E107432
Lin, S.-L.; Kuo, P.-Y.; Yang, D.-Y. 2007: Design and synthesis of a coumarin-based acidichromic colorant. Molecules 12(7): 1316-1324
Katsara, M.; Deraos, G.; Tselios, T.; Matsoukas, M.-T.; Friligou, I.; Matsoukas, J.; Apostolopoulos, V. 2009: Design and synthesis of a cyclic double mutant peptide (cyclo(87-99)[A91,A96]MBP87-99) induces altered responses in mice after conjugation to mannan: implications in the immunotherapy of multiple sclerosis. Journal of Medicinal Chemistry 52(1): 214-218
Léo, P.-M.; Morin, C.; Philouze, C. 2010: Design and synthesis of a cyclitol-derived scaffold with axial pyridyl appendages and its encapsulation of the silver(I) cation. Beilstein Journal of Organic Chemistry 6: 1022-1024
Wang, S.; Fang, W. 2011: Design and synthesis of a dual linker for solid phase synthesis of oleanolic acid derivatives. Molecules 16(6): 4748-4763
Ohshima, R.; Kitamura, M.; Morita, A.; Shiro, M.; Yamada, Y.; Ikekita, M.; Kimura, E.; Aoki, S. 2010: Design and synthesis of a fluorescent probe for Zn2+, 5,7-bis(N,N-dimethylaminosulfonyl)-8-hydroxyquinoline-pendant 1,4,7,10-tetraazacyclododecane and Zn2+-dependent hydrolytic and Zn2+-independent photochemical reactivation of its benzenesulfonyl-caged derivative. Inorganic Chemistry 49(3): 888-899
Zhan, Y.; Jia, G.; Wu, D.; Xu, Y.; Xu, L. 2009: Design and synthesis of a gossypol derivative with improved antitumor activities. Archiv der Pharmazie 342(4): 223-229
Li, X.; Qian, S.; He, Q.; Yang, B.; Li, J.; Hu, Y. 2010: Design and synthesis of a highly selective fluorescent turn-on probe for thiol bioimaging in living cells. Organic and Biomolecular Chemistry 8(16): 3627-3630
Kinoshita, K.; Asoh, K.; Furuichi, N.; Ito, T.; Kawada, H.; Hara, S.; Ohwada, J.; Miyagi, T.; Kobayashi, T.; Takanashi, K.; Tsukaguchi, T.; Sakamoto, H.; Tsukuda, T.; Oikawa, N. 2012: Design and synthesis of a highly selective, orally active and potent anaplastic lymphoma kinase inhibitor (CH5424802). Bioorganic and Medicinal Chemistry 20(3): 1271-1280
Hanaoka, K.; Muramatsu, Y.; Urano, Y.; Terai, T.; Nagano, T. 2010: Design and synthesis of a highly sensitive off-on fluorescent chemosensor for zinc ions utilizing internal charge transfer. Chemistry 16(2): 568-572
Hirano, K.; Macmillan, D.; Tezuka, K.; Tsuji, T.; Kajihara, Y. 2009: Design and synthesis of a homogeneous erythropoietin analogue with two human complex-type sialyloligosaccharides: combined use of chemical and bacterial protein expression methods. Angewandte Chemie 48(50): 9557-9560
Mills, A.D.; Yoo, C.; Butler, J.D.; Yang, B.; Verkman, A.S.; Kurth, M.J. 2010: Design and synthesis of a hybrid potentiator-corrector agonist of the cystic fibrosis mutant protein DeltaF508-CFTR. Bioorganic and Medicinal Chemistry Letters 20(1): 87-91
Nencini, A.; Castaldo, C.; Comery, T.A.; Dunlop, J.; Genesio, E.; Ghiron, C.; Haydar, S.; Maccari, L.; Micco, I.; Turlizzi, E.; Zanaletti, R.; Zhang, J. 2014: Design and synthesis of a hybrid series of potent and selective agonists of α7 nicotinic acetylcholine receptor. European Journal of Medicinal Chemistry 78: 401-418
Sunahara, H.; Urano, Y.; Kojima, H.; Nagano, T. 2007: Design and synthesis of a library of BODIPY-based environmental polarity sensors utilizing photoinduced electron-transfer-controlled fluorescence ON/OFF switching. Journal of the American Chemical Society 129(17): 5597-5604
Bhalay, G.; Albrecht, B.; Akhlaq, M.; Baettig, U.; Beer, D.; Brown, Z.; Charlton, S.; Dunstan, A.; Bradley, M.; Gedeck, P.; Glen, A.; Howe, T.; Keller, T.; Leighton-Davies, J.; Li, A.; McCarthy, C.; Mocquet, C.; Owen, C.; Nicklin, P.; Rosethorne, E. 2011: Design and synthesis of a library of chemokine antagonists. Bioorganic and Medicinal Chemistry Letters 21(21): 6249-6252
Schmitt, C.; Kail, D.; Mariano, M.; Empting, M.; Weber, N.; Paul, T.; Hartmann, R.W.; Engel, M. 2014: Design and synthesis of a library of lead-like 2,4-bisheterocyclic substituted thiophenes as selective Dyrk/Clk inhibitors. Plos one 9(3): E87851
Brummond, K.M.; Mao, S.; Shinde, S.N.; Johnston, P.J.; Day, B.W. 2009: Design and synthesis of a library of tetracyclic hydroazulenoisoindoles. Journal of Combinatorial Chemistry 11(3): 486-494
Huang, S.-T.; Teng, C.-J.; Lee, Y.-H.; Wu, J.-Y.; Wang, K.-L.; Lin, C.-M. 2010: Design and synthesis of a long-wavelength latent fluorogenic substrate for salicylate hydroxylase: a useful fluorimetric indicator for analyte determination by dehydrogenase-coupled biosensors. Analytical Chemistry 82(17): 7329-7334
Moromizato, S.; Hisamatsu, Y.; Suzuki, T.; Matsuo, Y.; Abe, R.; Aoki, S. 2012: Design and synthesis of a luminescent cyclometalated iridium(III) complex having N,N-diethylamino group that stains acidic intracellular organelles and induces cell death by photoirradiation. Inorganic Chemistry 51(23): 12697-12706
Yun, H.; Sim, J.; An, H.; Lee, J.; Lee, H.S.; Shin, Y.K.; Paek, S.-M.; Suh, Y.-G. 2014: Design and synthesis of a macrosphelide A-biotin chimera. Organic and Biomolecular Chemistry 12(36): 7127-7135
Sakami, S.; Kawai, K.; Maeda, M.; Aoki, T.; Fujii, H.; Ohno, H.; Ito, T.; Saitoh, A.; Nakao, K.; Izumimoto, N.; Matsuura, H.; Endo, T.; Ueno, S.; Natsume, K.; Nagase, H. 2008: Design and synthesis of a metabolically stable and potent antitussive agent, a novel delta opioid receptor antagonist, TRK-851. Bioorganic and Medicinal Chemistry 16(17): 7956-7967
Han, J.; Lee, T.H.; Tung, C.-H.; Lee, D.Y. 2014: Design and synthesis of a mitochondria-targeting carrier for small molecule drugs. Organic and Biomolecular Chemistry 12(48): 9793-9796
Malik, R.; Qian, S.; Law, B. 2011: Design and synthesis of a near-infrared fluorescent nanofiber precursor for detecting cell-secreted urokinase activity. Analytical Biochemistry 412(1): 26-33
Sharma, M.; Chauhan, K.; Srivastava, R.K.; Singh, S.V.; Srivastava, K.; Saxena, J.K.; Puri, S.K.; Chauhan, P.M.S. 2014: Design and synthesis of a new class of 4-aminoquinolinyl- and 9-anilinoacridinyl Schiff base hydrazones as potent antimalarial agents. Chemical Biology and Drug Design 84(2): 175-181
Tang, H.; Yan, Y.; Feng, Z.; de Jesus, R.K.; Yang, L.; Levorse, D.A.; Owens, K.A.; Akiyama, T.E.; Bergeron, R.; Castriota, G.A.; Doebber, T.W.; Ellsworth, K.P.; Lassman, M.E.; Li, C.; Wu, M.S.; Zhang, B.B.; Chapman, K.T.; Mills, S.G.; Berger, J.P.; Pasternak, A. 2010: Design and synthesis of a new class of malonyl-CoA decarboxylase inhibitors with anti-obesity and anti-diabetic activities. Bioorganic and Medicinal Chemistry Letters 20(20): 6088-6092
Hapuarachchige, S.; Montaño, G.; Ramesh, C.; Rodriguez, D.; Henson, L.H.; Williams, C.C.; Kadavakkollu, S.; Johnson, D.L.; Shuster, C.B.; Arterburn, J.B. 2011: Design and synthesis of a new class of membrane-permeable triazaborolopyridinium fluorescent probes. Journal of the American Chemical Society 133(17): 6780-6790
Wong, H-Lai.; Ko, C-Chiu.; Lam, W.Han.; Zhu, N.; Yam, V.Wing-Wah. 2009: Design and synthesis of a new class of photochromic diarylethene-containing dithieno[3,2-b:2',3'-d]pyrroles and their switchable luminescence properties. Chemistry 15(39): 10005-10009
Stragies, R.; Osterkamp, F.; Zischinsky, G.; Vossmeyer, D.; Kalkhof, H.; Reimer, U.; Zahn, G. 2007: Design and synthesis of a new class of selective integrin alpha5beta1 antagonists. Journal of Medicinal Chemistry 50(16): 3786-3794
Franceschin, M.; Nocioni, D.; Biroccio, A.; Micheli, E.; Cacchione, S.; Cingolani, C.; Venditti, A.; Zizza, P.; Bianco, A.; Altieri, A. 2014: Design and synthesis of a new dimeric xanthone derivative: enhancement of G-quadruplex selectivity and telomere damage. Organic and Biomolecular Chemistry 12(47): 9572-9582
Nenajdenko, V.G.; Goldberg, A.A.; Muzalevskiy, V.M.; Balenkova, E.S.; Shastin, A.V. 2013: Design and synthesis of a new family of fluorinated liquid crystals. Chemistry 19(7): 2370-2383
Sun, Y.-L.; Ablimit, A.; Zhai, H.-F.; Bao, J.-K.; Tang, Z.-T.; Wang, X.-B.; Wang, N.-L.; Feng, C.-M.; Cao, G.-H. 2014: Design and synthesis of a new layered thermoelectric material LaPbBiS3O. Inorganic Chemistry 53(20): 11125-11129
Liu, Y.; Meng, G.; Zheng, A.; Chen, F.; Chen, W.; De Clercq, E.; Pannecouque, C.; Balzarini, J. 2014: Design and synthesis of a new series of cyclopropylamino-linking diarylpyrimidines as HIV non-nucleoside reverse transcriptase inhibitors. European Journal of Pharmaceutical Sciences: Official Journal of the European Federation for Pharmaceutical Sciences 62: 334-341
Meng, G.; Liu, Y.; Zheng, A.; Chen, F.; Chen, W.; De Clercq, E.; Pannecouque, C.; Balzarini, J. 2014: Design and synthesis of a new series of modified CH-diarylpyrimidines as drug-resistant HIV non-nucleoside reverse transcriptase inhibitors. European Journal of Medicinal Chemistry 82: 600-611
Ye, Z.; Xiao, Y.; Song, B.; Yuan, J. 2014: Design and synthesis of a new terbium complex-based luminescent probe for time-resolved luminescence sensing of zinc ions. Journal of Fluorescence 24(5): 1537-1544
Buller, F.; Mannocci, L.; Zhang, Y.; Dumelin, C.E.; Scheuermann, Jörg.; Neri, D. 2008: Design and synthesis of a novel DNA-encoded chemical library using Diels-Alder cycloadditions. Bioorganic and Medicinal Chemistry Letters 18(22): 5926-5931
Mishra, A.; Pootrakulchote, N.; Fischer, M.K.R.; Klein, C.; Nazeeruddin, M.K.; Zakeeruddin, S.M.; Bäuerle, P.; Grätzel, M. 2009: Design and synthesis of a novel anchoring ligand for highly efficient thin film dye-sensitized solar cells. Chemical Communications 46: 7146-7148
Kotha, S.; Shah, V.R.; Mishra, P.P.; Datta, A. 2008: Design and synthesis of a novel anthracene-based fluorescent probe through the application of the Suzuki-Miyaura cross-coupling reaction. Amino Acids 35(1): 169-173
Rahmat, D.; Sakloetsakun, D.; Shahnaz, G.; Perera, G.; Kaindl, R.; Bernkop-Schnürch, A. 2011: Design and synthesis of a novel cationic thiolated polymer. International Journal of Pharmaceutics 411(1-2): 10-17
Suzuki, Y.; Oishi, S.; Takei, Y.; Yasue, M.; Misu, R.; Naoe, S.; Hou, Z.; Kure, T.; Nakanishi, I.; Ohno, H.; Hirasawa, A.; Tsujimoto, G.; Fujii, N. 2012: Design and synthesis of a novel class of CK2 inhibitors: application of copper- and gold-catalysed cascade reactions for fused nitrogen heterocycles. Organic and Biomolecular Chemistry 10(25): 4907-4915
Sasaki, H.; Hanaoka, K.; Urano, Y.; Terai, T.; Nagano, T. 2011: Design and synthesis of a novel fluorescence probe for Zn2+ based on the spirolactam ring-opening process of rhodamine derivatives. Bioorganic and Medicinal Chemistry 19(3): 1072-1078
Suzuki, Y.; Takagi, N.; Sano, T.; Chimuro, T. 2013: Design and synthesis of a novel fluorescent protein probe for easy and rapid electrophoretic gel staining by using a commonly available UV-based fluorescent imaging system. Electrophoresis 34(17): 2464-2472
Nohara, T.; Imamura, A.; Yamaguchi, M.; Hidari, K.I.P.J.; Suzuki, T.; Komori, T.; Ando, H.; Ishida, H.; Kiso, M. 2012: Design and synthesis of a novel ganglioside ligand for influenza a viruses. Molecules 17(8): 9590-9620
Le, P.T.; Cheng, H.; Ninkovic, S.; Plewe, M.; Huang, X.; Wang, H.; Bagrodia, S.; Sun, S.; Knighton, D.R.; LaFleur Rogers, C.M.; Pannifer, A.; Greasley, S.; Dalvie, D.; Zhang, E. 2012: Design and synthesis of a novel pyrrolidinyl pyrido pyrimidinone derivative as a potent inhibitor of PI3Kα and mTOR. Bioorganic and Medicinal Chemistry Letters 22(15): 5098-5103
Diaz, P.; Xu, J.; Astruc-Diaz, F.; Pan, H.-M.; Brown, D.L.; Naguib, M. 2008: Design and synthesis of a novel series of N-alkyl isatin acylhydrazone derivatives that act as selective cannabinoid receptor 2 agonists for the treatment of neuropathic pain. Journal of Medicinal Chemistry 51(16): 4932-4947
Bischoff, F.; Berthelot, D.; De Cleyn, M.; Macdonald, G.; Minne, G.; Oehlrich, D.; Pieters, S.; Surkyn, M.; Trabanco, A.és.A.; Tresadern, G.; Van Brandt, S.; Velter, I.; Zaja, M.; Borghys, H.; Masungi, C.; Mercken, M.; Gijsen, H.J.M. 2012: Design and synthesis of a novel series of bicyclic heterocycles as potent γ-secretase modulators. Journal of Medicinal Chemistry 55(21): 9089-9106
Jiménez-Alonso, S.; Orellana, H.C.áv.; Estévez-Braun, A.; Ravelo, A.G.; Pérez-Sacau, E.; Machín, F. 2008: Design and synthesis of a novel series of pyranonaphthoquinones as topoisomerase Ii catalytic inhibitors. Journal of Medicinal Chemistry 51(21): 6761-6772
Huang, K.; Zhang, X.; Emge, T.J.; Hou, G.; Cao, B.; Zhang, X. 2010: Design and synthesis of a novel three-hindered quadrant bisphosphine ligand and its application in asymmetric hydrogenation. Chemical Communications 46(45): 8555-8557
Li, Y.; Cao, R.; Lippard, S.J. 2011: Design and synthesis of a novel triptycene-based ligand for modeling carboxylate-bridged diiron enzyme active sites. Organic Letters 13(19): 5052-5055
Bowers, S.; Truong, A.P.; Neitz, R.J.; Neitzel, M.; Probst, G.D.; Hom, R.K.; Peterson, B.; Galemmo, R.A.; Konradi, A.W.; Sham, H.L.; Tóth, G.; Pan, H.; Yao, N.; Artis, D.R.; Brigham, E.F.; Quinn, K.P.; Sauer, J.-M.; Powell, K.; Ruslim, L.; Ren, Z.; Bard, F.éd.ér.; Yednock, T.A.; Griswold-Prenner, I. 2011: Design and synthesis of a novel, orally active, brain penetrant, tri-substituted thiophene based JNK inhibitor. Bioorganic and Medicinal Chemistry Letters 21(6): 1838-1843
Hagiwara, Y.; Mesch, R.A.; Kawakami, T.; Okazaki, M.; Jockusch, S.; Li, Y.; Turro, N.J.; Grant Willson, C. 2013: Design and synthesis of a photoaromatization-based two-stage photobase generator for pitch division lithography. Journal of Organic Chemistry 78(5): 1730-1734
Aoki, S.; Matsuo, N.; Hanaya, K.; Yamada, Y.; Kageyama, Y. 2009: Design and synthesis of a photocleavable biotin-linker for the photoisolation of ligand-receptor complexes based on the photolysis of 8-quinolinyl sulfonates in aqueous solution. Bioorganic and Medicinal Chemistry 17(9): 3405-3413
Viehmann, P.; Hecht, S. 2012: Design and synthesis of a photoswitchable guanidine catalyst. Beilstein Journal of Organic Chemistry 8: 1825-1830
Lai, Y.; Xie, C.; Zhang, Z.; Lu, W.; Ding, J. 2010: Design and synthesis of a potent peptide containing both specific and non-specific cell-adhesion motifs. Biomaterials 31(18): 4809-4817
Marian, C.; Huang, R.; Borch, R.F. 2011: Design and synthesis of a potential SH2 domain inhibitor bearing a stereodiversified 1,4-cis-enediol scaffold. Tetrahedron 67(52): 10216-10221
Hansen, L.H.; Bentzon-Tilia, M.; Bentzon-Tilia, S.; Norman, A.; Rafty, L.; Sørensen, S.ør.J. 2011: Design and synthesis of a quintessential self-transmissible IncX1 plasmid, pX1.0. Plos one 6(5): E19912
Liu, Z.; Zhang, C.; Wang, X.; He, W.; Guo, Z. 2012: Design and synthesis of a ratiometric fluorescent chemosensor for Cu(II) with a fluorophore hybridization approach. Organic Letters 14(17): 4378-4381
Qian, W.-J.; Burke, T.R. 2013: Design and synthesis of a reagent for solid-phase incorporation of the phosphothreonine mimetic (2S,3R)-2-amino-3-methyl-4-phosphonobutyric acid (Pmab) into peptides in a bio-reversible phosphonyl-bis-pivaloyloxymethyl (POM) prodrug form. Amino Acids 45(5): 1143-1148
Yu, X.; Zhang, R.; Ye, Z.; Song, B.; Yuan, J. 2013: Design and synthesis of a ruthenium(II) complex-based luminescent probe for highly selective and sensitive luminescence detection of nitric oxide. Journal of Fluorescence 23(6): 1113-1120
Chini, M.G.; De Simone, R.; Bruno, I.; Riccio, R.; Dehm, F.; Weinigel, C.; Barz, D.; Werz, O.; Bifulco, G. 2012: Design and synthesis of a second series of triazole-based compounds as potent dual mPGES-1 and 5-lipoxygenase inhibitors. European Journal of Medicinal Chemistry 54: 311-323
Guckian, K.M.; Lin, E.Y.-S.; Silvian, L.; Friedman, J.E.; Chin, D.; Scott, D.M. 2008: Design and synthesis of a series of meta aniline-based LFA-1 ICAM inhibitors. Bioorganic and Medicinal Chemistry Letters 18(19): 5249-5251
Chen, S.; Zhang, X.; Wang, J.; Wan, S.; Geng, M.; Jiang, T. 2011: Design and synthesis of a series of novel bisquinazoline glycosides as epidermal growth factor receptor inhibitors. Chemical Biology and Drug Design 78(6): 1006-1013
François, I.E.; Thevissen, K.; Pellens, K.; Meert, E.M.; Heeres, J.; Freyne, E.; Coesemans, E.; Viellevoye, M.; Deroose, F.; Martinez Gonzalez, S.; Pastor, J.; Corens, D.; Meerpoel, L.; Borgers, M.; Ausma, J.; Dispersyn, G.D.; Cammue, B.P. 2009: Design and synthesis of a series of piperazine-1-carboxamidine derivatives with antifungal activity resulting from accumulation of endogenous reactive oxygen species. Chemmedchem 4(10): 1714-1721
Gong, H.; Qi, H.; Sun, W.; Zhang, Y.; Jiang, D.; Xiao, J.; Yang, X.; Wang, Y.; Li, S. 2012: Design and synthesis of a series of pyrido[2,3-d]pyrimidine derivatives as CCR4 antagonists. Molecules 17(8): 9961-9970
Ohashi, M.; Oyama, T.; Putranto, E.W.; Waku, T.; Nobusada, H.; Kataoka, K.; Matsuno, K.; Yashiro, M.; Morikawa, K.; Huh, N.-H.; Miyachi, H. 2013: Design and synthesis of a series of α-benzyl phenylpropanoic acid-type peroxisome proliferator-activated receptor (PPAR) gamma partial agonists with improved aqueous solubility. Bioorganic and Medicinal Chemistry 21(8): 2319-2332
Crisóstomo, F.R.P.; Feng, Y.; Zhu, X.; Welsh, K.; An, J.; Reed, J.C.; Huang, Z. 2009: Design and synthesis of a simplified inhibitor for XIAP-BIR3 domain. Bioorganic and Medicinal Chemistry Letters 19(22): 6413-6418
Turner, W.W.; Hartvigsen, K.; Boullier, A.; Montano, E.N.; Witztum, J.L.; VanNieuwenhze, M.S. 2012: Design and synthesis of a stable oxidized phospholipid mimic with specific binding recognition for macrophage scavenger receptors. Journal of Medicinal Chemistry 55(18): 8178-8182
Zulkefeli, M.; Sogon, T.; Takeda, K.; Kimura, E.; Aoki, S. 2009: Design and synthesis of a stable supramolecular trigonal prism formed by the self-assembly of a linear tetrakis(Zn2+-cyclen) complex and trianionic trithiocyanuric acid in aqueous solution and its complexation with DNA (cyclen = 1,4,7,10-tetraazacyclododecane). Inorganic Chemistry 48(19): 9567-9578
Cui, G.; Ye, Z.; Zhang, R.; Wang, G.; Yuan, J. 2012: Design and synthesis of a terbium(III) complex-based luminescence probe for time-gated luminescence detection of mercury(II) ions. Journal of Fluorescence 22(1): 261-267
Dungan, V.J.; Ortin, Y.; Mueller-Bunz, H.; Rutledge, P.J. 2010: Design and synthesis of a tetradentate '3-amine-1-carboxylate' ligand to mimic the metal binding environment at the non-heme iron(II) oxidase active site. Organic and Biomolecular Chemistry 8(7): 1666-1673
Zhang, Y.; Liu, C.; Chou, C.J.; Wang, X.; Jia, Y.; Xu, W. 2013: Design and synthesis of a tetrahydroisoquinoline-based hydroxamate derivative (ZYJ-34v), an oral active histone deacetylase inhibitor with potent antitumor activity. Chemical Biology and Drug Design 82(2): 125-130
Guiard, J.; Paszkiewicz, E.; Sadowska, J.; Bundle, D.R. 2013: Design and synthesis of a universal antigen to detect brucellosis. Angewandte Chemie 52(28): 7181-7185
Ye, Y.Q.; Onose, J.-i.; Abe, N.; Koshino, H.; Takahashi, S. 2012: Design and synthesis of a vialinin a analog with a potent inhibitory activity of TNF-α production and its transformation into a couple of bioprobes. Bioorganic and Medicinal Chemistry Letters 22(7): 2385-2387
Cendret, V.; François-Heude, M.; Méndez-Ardoy, A.; Moreau, V.; Fernández, J.é M.G.ía.; Djedaïni-Pilard, F. 2012: Design and synthesis of a "click" high-mannose oligosaccharide mimic emulating Man8 binding affinity towards Con a. Chemical Communications 48(31): 3733-3735
Li, H.; Marcelo, F.; Bello, C.; Vogel, P.; Butters, T.D.; Rauter, A.él.P.; Zhang, Y.; Sollogoub, M.; Blériot, Y. 2009: Design and synthesis of acetamido tri- and tetra-hydroxyazepanes: potent and selective beta-N-acetylhexosaminidase inhibitors. Bioorganic and Medicinal Chemistry 17(15): 5598-5604
Lin, Y.-S.; Park, J.; De Schutter, J.W.; Huang, X.F.; Berghuis, A.M.; Sebag, M.; Tsantrizos, Y.S. 2012: Design and synthesis of active site inhibitors of the human farnesyl pyrophosphate synthase: apoptosis and inhibition of ERK phosphorylation in multiple myeloma cells. Journal of Medicinal Chemistry 55(7): 3201-3215
Eduardo-Canosa, S.; Fraga, R.ón.; Sigüeiro, R.; Marco, M.; Rochel, N.; Moras, D.; Mouriño, A. 2010: Design and synthesis of active vitamin D analogs. Journal of Steroid Biochemistry and Molecular Biology 121(1-2): 7-12
Ye, L.; Xu, A.; Cheng, C.; Zhang, L.; Huo, C.; Huang, F.; Xu, H.; Li, R. 2011: Design and synthesis of affinity ligands and relation of their structure with adsorption of proteins. Journal of Separation Science 34(22): 3145-3150
Gim, H.J.; Li, H.; Lee, E.; Ryu, J.-H.; Jeon, R. 2013: Design and synthesis of alkoxyindolyl-3-acetic acid analogs as peroxisome proliferator-activated receptor-γ/δ agonists. Bioorganic and Medicinal Chemistry Letters 23(2): 513-517
Cluzeau, J.ér.ôm.; Oishi, S.; Ohno, H.; Wang, Z.; Evans, B.; Peiper, S.C.; Fujii, N. 2007: Design and synthesis of all diastereomers of cyclic pseudo-dipeptides as mimics of cyclic CXCR4 pentapeptide antagonists. Organic and Biomolecular Chemistry 5(12): 1915-1923
Garner, J.; Harding, M.M. 2007: Design and synthesis of alpha-helical peptides and mimetics. Organic and Biomolecular Chemistry 5(22): 3577-3585
Chen, J.-C.; Uang, B.-J.; Lyu, P.-C.; Chang, J.-Y.; Liu, K.-J.; Kuo, C.-C.; Hsieh, H.-P.; Wang, H.-C.; Cheng, C.-S.; Chang, Y.-H.; Chang, M.D.-T.; Chang, W.-S.W.; Lin, C.-C. 2010: Design and synthesis of alpha-ketoamides as cathepsin S inhibitors with potential applications against tumor invasion and angiogenesis. Journal of Medicinal Chemistry 53(11): 4545-4549
Tan, X.; Wang, P.; Nian, S.; Wang, G. 2014: Design and synthesis of amide derivatives as S-adenosyl-L-homocysteine hydrolase inhibitors. Chemical and Pharmaceutical Bulletin 62(1): 112-117
Inokuchi, E.; Yamada, A.; Hozumi, K.; Tomita, K.; Oishi, S.; Ohno, H.; Nomizu, M.; Fujii, N. 2011: Design and synthesis of amidine-type peptide bond isosteres: application of nitrile oxide derivatives as active ester equivalents in peptide and peptidomimetics synthesis. Organic and Biomolecular Chemistry 9(9): 3421-3427
Malamas, M.S.; Robichaud, A.; Erdei, J.; Quagliato, D.; Solvibile, W.; Zhou, P.; Morris, K.; Turner, J.; Wagner, E.; Fan, K.; Olland, A.; Jacobsen, S.; Reinhart, P.; Riddell, D.; Pangalos, M. 2010: Design and synthesis of aminohydantoins as potent and selective human β-secretase (BACE1) inhibitors with enhanced brain permeability. Bioorganic and Medicinal Chemistry Letters 20(22): 6597-6605
Kamal, A.; Kumar, G.B.; Polepalli, S.; Shaik, A.B.; Reddy, V.S.; Reddy, M.K.; Reddy, C.R.; Mahesh, R.; Kapure, J.S.; Jain, N. 2014: Design and synthesis of aminostilbene-arylpropenones as tubulin polymerization inhibitors. Chemmedchem 9(11): 2565-2579
Zou, H.; Koh, J.-J.; Li, J.; Qiu, S.; Aung, T.T.; Lin, H.; Lakshminarayanan, R.; Dai, X.; Tang, C.; Lim, F.H.; Zhou, L.; Tan, A.L.; Verma, C.; Tan, D.T.H.; Chan, H.S.O.; Saraswathi, P.; Cao, D.; Liu, S.; Beuerman, R.W. 2013: Design and synthesis of amphiphilic xanthone-based, membrane-targeting antimicrobials with improved membrane selectivity. Journal of Medicinal Chemistry 56(6): 2359-2373
Hakamata, W.; Machida, A.; Oku, T.; Nishio, T. 2011: Design and synthesis of an ER-specific fluorescent probe based on carboxylesterase activity with quinone methide cleavage process. Bioorganic and Medicinal Chemistry Letters 21(11): 3206-3209
Eerland, M.F.; Hedberg, C. 2012: Design and synthesis of an Fmoc-SPPS-compatible amino acid building block mimicking the transition state of phosphohistidine phosphatase. Journal of Organic Chemistry 77(4): 2047-2052
Kumar, N.S.; Young, R.N. 2009: Design and synthesis of an all-in-one 3-(1,1-difluoroprop-2-ynyl)-3H-diazirin-3-yl functional group for photo-affinity labeling. Bioorganic and Medicinal Chemistry 17(15): 5388-5395
Kobayashi, T.; Iwama, S.; Fusano, A.; Kato, Y.; Ikeda, A.; Teranishi, Y.; Nishihara, A.; Tobe, M. 2014: Design and synthesis of an aminopiperidine series of γ-secretase modulators. Bioorganic and Medicinal Chemistry Letters 24(1): 378-381
Yoshino, H.; Sato, H.; Shiraishi, T.; Tachibana, K.; Emura, T.; Honma, A.; Ishikura, N.; Tsunenari, T.; Watanabe, M.; Nishimoto, A.; Nakamura, R.; Nakagawa, T.; Ohta, M.; Takata, N.; Furumoto, K.; Kimura, K.; Kawata, H. 2010: Design and synthesis of an androgen receptor pure antagonist (CH5137291) for the treatment of castration-resistant prostate cancer. Bioorganic and Medicinal Chemistry 18(23): 8150-8157
Rutledge, R.D.; Huffman, B.J.; Cliffel, D.E.; Wright, D.W. 2008: Design and synthesis of an antigenic mimic of the Ebola glycoprotein. Journal of Materials Research 23(12): 3161-3168
Chen, J.-R.; Yang, D.-Y. 2009: Design and synthesis of an o-hydroxyphenyl-containing spiropyran thermochromic colorant. Organic Letters 11(8): 1769-1772
Midya, G.C.; Paladhi, S.; Bhowmik, S.; Saha, S.; Dash, J. 2013: Design and synthesis of an on-off "click" fluorophore that executes a logic operation and detects heavy and transition metal ions in water and living cells. Organic and Biomolecular Chemistry 11(18): 3057-3063
Dhanya, R.-P.; Sidique, S.; Sheffler, D.J.; Nickols, H.H.; Herath, A.; Yang, L.; Dahl, R.; Ardecky, R.; Semenova, S.; Markou, A.; Conn, P.J.; Cosford, N.D.P. 2011: Design and synthesis of an orally active metabotropic glutamate receptor subtype-2 (mGluR2) positive allosteric modulator (PAM) that decreases cocaine self-administration in rats. Journal of Medicinal Chemistry 54(1): 342-353
Zhou, H.-J.; Aujay, M.A.; Bennett, M.K.; Dajee, M.; Demo, S.D.; Fang, Y.; Ho, M.N.; Jiang, J.; Kirk, C.J.; Laidig, G.J.; Lewis, E.R.; Lu, Y.; Muchamuel, T.; Parlati, F.; Ring, E.; Shenk, K.D.; Shields, J.; Shwonek, P.J.; Stanton, T.; Sun, C.M.; Sylvain, C.; Woo, T.M.; Yang, J. 2009: Design and synthesis of an orally bioavailable and selective peptide epoxyketone proteasome inhibitor (PR-047). Journal of Medicinal Chemistry 52(9): 3028-3038
Marton, J.án.; Henriksen, G. 2012: Design and synthesis of an ¹⁸F-labeled version of phenylethyl orvinol ([¹⁸F]FE-PEO) for PET-imaging of opioid receptors. Molecules 17(10): 11554-11569
Zhou, J.; Geng, G.; Shi, Q.; Sauriol, F.; Wu, J.H. 2009: Design and synthesis of androgen receptor antagonists with bulky side chains for overcoming antiandrogen resistance. Journal of Medicinal Chemistry 52(17): 5546-5550
Goto, T.; Ohta, K.; Fujii, S.; Ohta, S.; Endo, Y. 2010: Design and synthesis of androgen receptor full antagonists bearing a p-carborane cage: promising ligands for anti-androgen withdrawal syndrome. Journal of Medicinal Chemistry 53(13): 4917-4926
González-Chávez, M.M.ín.; Méndez, F.; Martínez, R.; Pérez-González, C.úh.; Martínez-Gutiérrez, F. 2010: Design and synthesis of anti-MRSA benzimidazolylbenzene-sulfonamides. QSAR studies for prediction of antibacterial activity. Molecules 16(1): 175-189
Solomon, V.R.; Hu, C.; Lee, H. 2010: Design and synthesis of anti-breast cancer agents from 4-piperazinylquinoline: a hybrid pharmacophore approach. Bioorganic and Medicinal Chemistry 18(4): 1563-1572
Tahoori, F.; Balalaie, S.; Sheikhnejad, R.; Sadjadi, M.; Boloori, P. 2014: Design and synthesis of anti-cancer cyclopeptides containing triazole skeleton. Amino Acids 46(4): 1033-1046
Garner, J.; Harding, M.M. 2010: Design and synthesis of antifreeze glycoproteins and mimics. Chembiochem: a European Journal of Chemical Biology 11(18): 2489-2498
Sheng, C.; Che, X.; Wang, W.; Wang, S.; Cao, Y.; Yao, J.; Miao, Z.; Zhang, W. 2011: Design and synthesis of antifungal benzoheterocyclic derivatives by scaffold hopping. European Journal of Medicinal Chemistry 46(5): 1706-1712
Koufaki, M.; Detsi, A. 2010: Design and synthesis of antioxidant alpha-lipoic acid hybrids. Methods in Molecular Biology 594: 297-309
Li, J.-q.; Huang, L.-y.; Chen, J.-x.; Weng, Z.-j.; Zhang, C.-n. 2007: Design and synthesis of aralkyl-ketone piperazine derivatives and their antalgic activities. Yao Xue Xue Bao 42(11): 1166-1175
Pabba, C.; Gregg, B.T.; Kitchen, D.B.; Chen, Z.J.; Judkins, A. 2011: Design and synthesis of aryl ether and sulfone hydroxamic acids as potent histone deacetylase (HDAC) inhibitors. Bioorganic and Medicinal Chemistry Letters 21(1): 324-328
Tipparaju, S.K.; Mulhearn, D.C.; Klein, G.M.; Chen, Y.; Tapadar, S.; Bishop, M.H.; Yang, S.; Chen, J.; Ghassemi, M.; Santarsiero, B.D.; Cook, J.L.; Johlfs, M.; Mesecar, A.D.; Johnson, M.E.; Kozikowski, A.P. 2008: Design and synthesis of aryl ether inhibitors of the Bacillus anthracis enoyl-ACP reductase. Chemmedchem 3(8): 1250-1268
Futatsugi, K.; Piotrowski, D.W.; Casimiro-Garcia, A.; Robinson, S.; Sammons, M.; Loria, P.M.; Banker, M.E.; Petersen, D.N.; Schmidt, N.J. 2013: Design and synthesis of aryl sulfonamide-based nonsteroidal mineralocorticoid receptor antagonists. Bioorganic and Medicinal Chemistry Letters 23(23): 6239-6242
Ali, S.; Rasool, N.; Ullah, A.; Nasim, F.-u.-H.; Yaqoob, A.; Zubair, M.; Rashid, U.; Riaz, M. 2013: Design and synthesis of arylthiophene-2-carbaldehydes via Suzuki-Miyaura reactions and their biological evaluation. Molecules 18(12): 14711-14725
Dhiman, R.; Sharma, S.; Singh, G.; Nepali, K.; Singh Bedi, P.M. 2013: Design and synthesis of aza-flavones as a new class of xanthine oxidase inhibitors. Archiv der Pharmazie 346(1): 7-16
Gim, H.J.; Li, H.; Jung, S.R.; Park, Y.J.; Ryu, J.-H.; Chung, K.H.; Jeon, R. 2014: Design and synthesis of azaisoflavone analogs as phytoestrogen mimetics. European Journal of Medicinal Chemistry 85: 107-118
El-Gazzar, A.B.A.; Youssef, M.M.; Youssef, A.M.S.; Abu-Hashem, A.A.; Badria, F.A. 2009: Design and synthesis of azolopyrimidoquinolines, pyrimidoquinazolines as anti-oxidant, anti-inflammatory and analgesic activities. European Journal of Medicinal Chemistry 44(2): 609-624
Qvit, N.; Hatzubai, A.; Shalev, D.E.; Ben-Neriah, Y.; Gilon, C. 2009: Design and synthesis of backbone cyclic phosphopeptides: the IkappaB model. Advances in Experimental Medicine and Biology 611: 139-140
Qvit, N.; Hatzubai, A.; Shalev, D.E.; Friedler, A.; Ben-Neriah, Y.; Gilon, C. 2009: Design and synthesis of backbone cyclic phosphorylated peptides: the IkappaB model. Biopolymers 91(2): 157-168
Tang, G.; Lin, X.; Qiu, Z.; Li, W.; Zhu, L.; Wang, L.; Li, S.; Li, H.; Lin, W.; Yang, M.; Guo, T.; Chen, L.; Lee, D.; Wu, J.Z.; Yang, W. 2011: Design and synthesis of benzenesulfonamide derivatives as potent anti-influenza hemagglutinin inhibitors. Acs Medicinal Chemistry Letters 2(8): 603-607
Rathore, A.; Rahman, M.U.; Siddiqui, A.A.; Ali, A.; Shaharyar, M. 2014: Design and synthesis of benzimidazole analogs endowed with oxadiazole as selective COX-2 inhibitor. Archiv der Pharmazie 347(12): 923-935
Kamal, A.; Ramakrishna, G.; Lakshma Nayak, V.; Raju, P.; Subba Rao, A.V.; Viswanath, A.; Vishnuvardhan, M.V.P.S.; Ramakrishna, S.; Srinivas, G. 2012: Design and synthesis of benzo[c,d]indolone-pyrrolobenzodiazepine conjugates as potential anticancer agents. Bioorganic and Medicinal Chemistry 20(2): 789-800
Wei, L.; Gao, X.; Warne, R.; Hao, X.; Bussiere, D.; Gu, X.-j.; Uno, T.; Liu, Y. 2010: Design and synthesis of benzoazepin-2-one analogs as allosteric binders targeting the PIF pocket of PDK1. Bioorganic and Medicinal Chemistry Letters 20(13): 3897-3902
Kotha, S.; Chavan, A.S. 2010: Design and synthesis of benzosultine-sulfone as a o-xylylene precursor via cross-enyne metathesis and rongalite: further expansion to polycyclics via regioselective Diels-Alder reaction. Journal of Organic Chemistry 75(12): 4319-4322
Gim, H.J.; Cheon, Y.-J.; Ryu, J.-H.; Jeon, R. 2011: Design and synthesis of benzoxazole containing indole analogs as peroxisome proliferator-activated receptor-γ/δ dual agonists. Bioorganic and Medicinal Chemistry Letters 21(10): 3057-3061
Sun, R.; Liu, Y.; Zhang, Y.; Xiong, L.; Wang, Q. 2011: Design and synthesis of benzoylphenylureas with fluorinated substituents on the aniline ring as insect growth regulators. Journal of Agricultural and Food Chemistry 59(6): 2471-2477
Kumar, A.S.; Reddy, M.A.; Jain, N.; Kishor, C.; Murthy, T.R.; Ramesh, D.; Supriya, B.; Addlagatta, A.; Kalivendi, S.V.; Sreedhar, B. 2013: Design and synthesis of biaryl aryl stilbenes/ethylenes as antimicrotubule agents. European Journal of Medicinal Chemistry 60: 305-324
Oehlrich, D.; Rombouts, F.J.R.; Berthelot, D.; Bischoff, F.ço.P.; De Cleyn, M.A.J.; Jaroskova, L.; Macdonald, G.; Mercken, M.; Surkyn, M.; Trabanco, A.és.A.; Tresadern, G.; Van Brandt, S.; Velter, A.I.; Wu, T.; Gijsen, H.J.M. 2013: Design and synthesis of bicyclic heterocycles as potent γ-secretase modulators. Bioorganic and Medicinal Chemistry Letters 23(17): 4794-4800
Zhang, X.; Glunz, P.W.; Jiang, W.; Schmitt, A.; Newman, M.; Barbera, F.A.; Bozarth, J.M.; Rendina, A.R.; Wei, A.; Wen, X.; Rossi, K.A.; Luettgen, J.M.; Wong, P.C.; Knabb, R.M.; Wexler, R.R.; Scott Priestley, E. 2013: Design and synthesis of bicyclic pyrazinone and pyrimidinone amides as potent TF-FVIIa inhibitors. Bioorganic and Medicinal Chemistry Letters 23(6): 1604-1607
Aher, N.G.; Pore, V.S.; Mishra, N.N.; Shukla, P.K.; Gonnade, R.G. 2009: Design and synthesis of bile acid-based amino sterols as antimicrobial agents. Bioorganic and Medicinal Chemistry Letters 19(18): 5411-5414
Sokolova, N.V.; Latyshev, G.V.; Lukashev, N.V.; Nenajdenko, V.G. 2011: Design and synthesis of bile acid-peptide conjugates linked via triazole moiety. Organic and Biomolecular Chemistry 9(13): 4921-4926
Wang, C.; Chi, M.; Li, D.; Strmcnik, D.; van der Vliet, D.; Wang, G.; Komanicky, V.; Chang, K.-C.; Paulikas, A.P.; Tripkovic, D.; Pearson, J.; More, K.L.; Markovic, N.M.; Stamenkovic, V.R. 2011: Design and synthesis of bimetallic electrocatalyst with multilayered Pt-skin surfaces. Journal of the American Chemical Society 133(36): 14396-14403
Tada, S.; Kitajima, T.; Ito, Y. 2012: Design and synthesis of binding growth factors. International Journal of Molecular Sciences 13(5): 6053-6072
Zoidis, G.; Kolocouris, N.; Kelly, J.M.; Prathalingam, S.R.; Naesens, L.; De Clercq, E. 2010: Design and synthesis of bioactive adamantanaminoalcohols and adamantanamines. European Journal of Medicinal Chemistry 45(11): 5022-5030
Lim, E.-K.; Haam, S.; Lee, K.; Huh, Y.-M. 2011: Design and synthesis of biofunctionalized metallic/magnetic nanomaterials. Methods in Molecular Biology 751: 583-595
Bryan, A.; Joseph, L.; Bennett, J.A.; Jacobson, H.I.; Andersen, T.T. 2011: Design and synthesis of biologically active peptides: a 'tail' of amino acids can modulate activity of synthetic cyclic peptides. Peptides 32(12): 2504-2510
Biswas, A.; Bayer, I.S.; Zhao, H.; Wang, T.; Watanabe, F.; Biris, A.S. 2010: Design and synthesis of biomimetic multicomponent all-bone-minerals bionanocomposites. Biomacromolecules 11(10): 2545-2549
Mizuhara, T.; Oishi, S.; Ohno, H.; Shimura, K.; Matsuoka, M.; Fujii, N. 2013: Design and synthesis of biotin- or alkyne-conjugated photoaffinity probes for studying the target molecules of PD 404182. Bioorganic and Medicinal Chemistry 21(7): 2079-2087
Gu, M.; Yan, J.; Bai, Z.; Chen, Y.-T.; Lu, W.; Tang, J.; Duan, L.; Xie, D.; Nan, F.-J. 2010: Design and synthesis of biotin-tagged photoaffinity probes of jasmonates. Bioorganic and Medicinal Chemistry 18(9): 3012-3019
Saitoh, T.; Takeiri, M.; Gotoh, Y.; Ishikawa, Y.; Umezawa, K.; Nishiyama, S. 2011: Design and synthesis of biotinylated DHMEQ for direct identification of its target NF-κB components. Bioorganic and Medicinal Chemistry Letters 21(21): 6293-6296
Anraku, K.; Inoue, T.; Sugimoto, K.; Kudo, K.; Okamoto, Y.; Morii, T.; Mori, Y.; Otsuka, M. 2011: Design and synthesis of biotinylated inositol 1,3,4,5-tetrakisphosphate targeting Grp1 pleckstrin homology domain. Bioorganic and Medicinal Chemistry 19(22): 6833-6841
Anraku, K.; Inoue, T.; Sugimoto, K.; Morii, T.; Mori, Y.; Okamoto, Y.; Otsuka, M. 2008: Design and synthesis of biotinylated inositol phosphates relevant to the biotin-avidin techniques. Organic and Biomolecular Chemistry 6(10): 1822-1830
Bao, K.; Dai, Y.; Zhu, Z.-B.; Tu, F.-J.; Zhang, W.-G.; Yao, X.-S. 2010: Design and synthesis of biphenyl derivatives as mushroom tyrosinase inhibitors. Bioorganic and Medicinal Chemistry 18(18): 6708-6714
Lee, S.-H.; Chan, C.T.-L.; Wong, K.M.-C.; Lam, W.H.; Kwok, W.-M.; Yam, V.W.-W. 2014: Design and synthesis of bipyridine platinum(II) bisalkynyl fullerene donor-chromophore-acceptor triads with ultrafast charge separation. Journal of the American Chemical Society 136(28): 10041-10052
Jardosh, H.H.; Patel, M.P. 2013: Design and synthesis of biquinolone-isoniazid hybrids as a new class of antitubercular and antimicrobial agents. European Journal of Medicinal Chemistry 65: 348-359
Sechi, M.; Azzena, U.; Delussu, M.P.; Dallocchio, R.; Dessì, A.; Cosseddu, A.; Pala, N.; Neamati, N. 2008: Design and synthesis of bis-amide and hydrazide-containing derivatives of malonic acid as potential HIV-1 integrase inhibitors. Molecules 13(10): 2442-2461
Wilbur, D.S.; Park, S.I.; Chyan, M.-K.; Wan, F.; Hamlin, D.K.; Shenoi, J.; Lin, Y.; Wilbur, S.M.; Buchegger, F.; Pantelias, A.; Pagel, J.M.; Press, O.W. 2010: Design and synthesis of bis-biotin-containing reagents for applications utilizing monoclonal antibody-based pretargeting systems with streptavidin mutants. Bioconjugate Chemistry 21(7): 1225-1238
Kline, T.; Jackson, S.R.; Deng, W.; Verlinde, C.L.M.J.; Miller, S.I. 2008: Design and synthesis of bis-carbamate analogs of cyclic bis-(3'-5')-diguanylic acid (c-di-GMP) and the acyclic dimer PGPG. Nucleosides Nucleotides and Nucleic Acids 27(12): 1282-1300
Garre, S.; Parker, E.; Ni, B.; Headley, A.D. 2008: Design and synthesis of bistereogenic chiral ionic liquids and their use as solvents for asymmetric Baylis-Hillman reactions. Organic and Biomolecular Chemistry 6(17): 3041-3043
Fournier, D.; Poirier, D.; Mazumdar, M.; Lin, S.-X. 2008: Design and synthesis of bisubstrate inhibitors of type 1 17beta-hydroxysteroid dehydrogenase: overview and perspectives. European Journal of Medicinal Chemistry 43(11): 2298-2306
Das, B.C.; Tang, X.-Y.; Evans, T. 2012: Design and synthesis of boron containing potential pan-RAR inverse agonists. Tetrahedron Letters 53(11): 1316-1318
Zhang, Y.-K.; Plattner, J.J.; Akama, T.; Baker, S.J.; Hernandez, V.S.; Sanders, V.; Freund, Y.; Kimura, R.; Bu, W.; Hold, K.M.; Lu, X.-S. 2010: Design and synthesis of boron-containing PDE4 inhibitors using soft-drug strategy for potential dermatologic anti-inflammatory application. Bioorganic and Medicinal Chemistry Letters 20(7): 2270-2274
O'Connell, D.P.; LeBlanc, D.F.; Cromley, D.; Billheimer, J.; Rader, D.J.; Bachovchin, W.W. 2012: Design and synthesis of boronic acid inhibitors of endothelial lipase. Bioorganic and Medicinal Chemistry Letters 22(3): 1397-1401
Bowers, S.; Truong, A.P.; Jeffrey Neitz, R.; Hom, R.K.; Sealy, J.M.; Probst, G.D.; Quincy, D.; Peterson, B.; Chan, W.; Galemmo, R.A.; Konradi, A.W.; Sham, H.L.; Tóth, G.; Pan, H.; Lin, M.; Yao, N.; Artis, D.R.; Zhang, H.; Chen, L.; Dryer, M.; Samant, B.; Zmolek, W.; Wong, K.; Lorentzen, C.; Goldbach, E.; Tonn, G.; Quinn, K.P.; Sauer, J-Michael.; Wright, S.; Powell, K.; Ruslim, L.; Ren, Z.; Bard, Fédérique.; Yednock, T.A.; Griswold-Prenner, I. 2011: Design and synthesis of brain penetrant selective JNK inhibitors with improved pharmacokinetic properties for the prevention of neurodegeneration. Bioorganic and Medicinal Chemistry Letters 21(18): 5521-5527
Xu, X.-D.; Zhang, J.; Chen, L.-J.; Guo, R.; Wang, D.-X.; Yang, H.-B. 2012: Design and synthesis of branched platinum-acetylide complexes possessing a porphyrin core and their self-assembly behaviour. Chemical Communications 48(91): 11223-11225
Bodiwala, H.S.; Sabde, S.; Gupta, P.; Mukherjee, R.; Kumar, R.; Garg, P.; Bhutani, K.K.; Mitra, D.; Singh, I.P. 2011: Design and synthesis of caffeoyl-anilides as portmanteau inhibitors of HIV-1 integrase and CCR5. Bioorganic and Medicinal Chemistry 19(3): 1256-1263
Ikeda, S.; Kubota, T.; Wang, D.O.; Yanagisawa, H.; Umemoto, T.; Okamoto, A. 2011: Design and synthesis of caged fluorescent nucleotides and application to live-cell RNA imaging. Chembiochem: a European Journal of Chemical Biology 12(18): 2871-2880
Tanwar, J.; Datta, A.; Chauhan, K.; Kumaran, S.S.; Tiwari, A.K.; Kadiyala, K.G.; Pal, S.; Thirumal, M.; Mishra, A.K. 2014: Design and synthesis of calcium responsive magnetic resonance imaging agent: its relaxation and luminescence studies. European Journal of Medicinal Chemistry 82: 225-232
He, X.; Lam, W.H.; Zhu, N.; Yam, V.W.-W. 2009: Design and synthesis of calixarene-based bis-alkynyl-bridged dinuclear Au(I) isonitrile complexes as luminescent ion probes by the modulation of Au..au interactions. Chemistry 15(35): 8842-8851
Lee, K.Y.; Lee, K.S.; Jin, C.; Lee, Y.S. 2009: Design and synthesis of calpain inhibitory 6-pyridone 2-carboxamide derivatives. European Journal of Medicinal Chemistry 44(3): 1331-1334
Fulp, A.; Bortoff, K.; Seltzman, H.; Zhang, Y.; Mathews, J.; Snyder, R.; Fennell, T.; Maitra, R. 2012: Design and synthesis of cannabinoid receptor 1 antagonists for peripheral selectivity. Journal of Medicinal Chemistry 55(6): 2820-2834
Jin, G.H.; Lee, H.J.; Gim, H.J.; Ryu, J.-H.; Jeon, R. 2012: Design and synthesis of carbamate and thiocarbamate derivatives and their inhibitory activities of NO production in LPS activated macrophages. Bioorganic and Medicinal Chemistry Letters 22(9): 3301-3304
Kim, E.; Shen, G.Huan.; Hong, J.Hee. 2011: Design and synthesis of carbocyclic versions of furanoid nucleoside phosphonic Acid analogues as potential anti-hiv agents. Nucleosides Nucleotides and Nucleic Acids 30(10): 798-813
Wang, M.; Mickens, J.; Gao, M.; Miller, K.D.; Sledge, G.W.; Hutchins, G.D.; Zheng, Q.-H. 2009: Design and synthesis of carbon-11-labeled dual aromatase-steroid sulfatase inhibitors as new potential PET agents for imaging of aromatase and steroid sulfatase expression in breast cancer. Steroids 74(12): 896-905
Ohta, K.; Goto, T.; Fijii, S.; Suzuki, T.; Ohta, S.; Endo, Y. 2008: Design and synthesis of carborane-containing androgen receptor (AR) antagonist bearing a pyridine ring. Bioorganic and Medicinal Chemistry 16(17): 8022-8028
Yang, Z.; Li, D.; Li, T. 2011: Design and synthesis of catenated rings based on toroidal DNA structures. Chemical Communications 47(43): 11930-11932
Pang, Y.; Zhu, Q.; Liu, J.; Wu, J.; Wang, R.; Chen, S.; Zhu, X.; Yan, D.; Huang, W.; Zhu, B. 2010: Design and synthesis of cationic drug carriers based on hyperbranched poly(amine-ester)s. Biomacromolecules 11(3): 575-582
Sealy, J.M.; Truong, A.P.; Tso, L.; Probst, G.D.; Aquino, J.; Hom, R.K.; Jagodzinska, B.M.; Dressen, D.; Wone, D.W.G.; Brogley, L.; John, V.; Tung, J.S.; Pleiss, M.A.; Tucker, J.A.; Konradi, A.W.; Dappen, M.S.; Toth, G.; Pan, H.; Ruslim, L.; Miller, J.; Bova, M.P.; Sinha, S.; Quinn, K.P.; Sauer, J.-M. 2009: Design and synthesis of cell potent BACE-1 inhibitors: structure-activity relationship of P1' substituents. Bioorganic and Medicinal Chemistry Letters 19(22): 6386-6391
Trombino, S.; Cassano, R.; Bloise, E.; Muzzalupo, R.; Leta, S.; Puoci, F.; Picci, N. 2008: Design and synthesis of cellulose derivatives with antioxidant activity. Macromolecular Bioscience 8(1): 86-95
Hajra, S.; Bhowmick, M.; Maji, B.; Sinha, D. 2007: Design and synthesis of chiral N-chloroimidodicarbonates: application to asymmetric chlorination of silyl enol ethers. Journal of Organic Chemistry 72(13): 4872-4876
Itoh, S.; Sonoike, S.; Kitamura, M.; Aoki, S. 2014: Design and synthesis of chiral Zn2+ complexes mimicking natural aldolases for catalytic C-C bond forming reactions in aqueous solution. International Journal of Molecular Sciences 15(2): 2087-2118
Han, Z.S.; Herbage, M.A.; Mangunuru, H.P.R.; Xu, Y.; Zhang, L.; Reeves, J.T.; Sieber, J.D.; Li, Z.; DeCroos, P.; Zhang, Y.; Li, G.; Li, N.; Ma, S.; Grinberg, N.; Wang, X.; Goyal, N.; Krishnamurthy, D.; Lu, B.; Song, J.J.; Wang, G.; Senanayake, C.H. 2013: Design and synthesis of chiral oxathiozinone scaffolds: efficient synthesis of hindered enantiopure sulfinamides and sulfinyl ketimines. Angewandte Chemie 52(26): 6713-6717
Solomon, V.R.; Hu, C.; Lee, H. 2010: Design and synthesis of chloroquine analogs with anti-breast cancer property. European Journal of Medicinal Chemistry 45(9): 3916-3923
Yang, Q.; Chen, L.; He, X.; Gao, Z.; Shen, X.; Bai, D. 2008: Design and synthesis of cinanserin analogs as severe acute respiratory syndrome coronavirus 3CL protease inhibitors. Chemical and Pharmaceutical Bulletin 56(10): 1400-1405
Qiu, C.; Kumar, S.; Guo, J.; Yu, L.; Guo, W.; Shi, S.; Russo, J.J.; Ju, J. 2012: Design and synthesis of cleavable biotinylated dideoxynucleotides for DNA sequencing by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. Analytical Biochemistry 427(2): 193-201
Coleman, P.J.; Schreier, J.D.; McGaughey, G.B.; Bogusky, M.J.; Cox, C.D.; Hartman, G.D.; Ball, R.G.; Harrell, C.M.; Reiss, D.R.; Prueksaritanont, T.; Winrow, C.J.; Renger, J.J. 2010: Design and synthesis of conformationally constrained N,N-disubstituted 1,4-diazepanes as potent orexin receptor antagonists. Bioorganic and Medicinal Chemistry Letters 20(7): 2311-2315
Nishikawa, K.; Fukuda, H.; Abe, M.; Nakanishi, K.; Tazawa, Y.; Yamaguchi, C.; Hiradate, S.; Fujii, Y.; Okuda, K.; Shindo, M. 2013: Design and synthesis of conformationally constrained analogues of cis-cinnamic acid and evaluation of their plant growth inhibitory activity. Phytochemistry 96: 223-234
Dunsmore, C.J.; Malone, K.J.; Bailey, K.R.; Wear, M.A.; Florance, H.; Shirran, S.; Barran, P.E.; Page, A.P.; Walkinshaw, M.D.; Turner, N.J. 2011: Design and synthesis of conformationally constrained cyclophilin inhibitors showing a cyclosporin-A phenotype in C. elegans. Chembiochem: a European Journal of Chemical Biology 12(5): 802-810
Gomez, R.; Jolly, S.J.; Williams, T.; Vacca, J.P.; Torrent, M.; McGaughey, G.; Lai, M.-T.; Felock, P.; Munshi, V.; Distefano, D.; Flynn, J.; Miller, M.; Yan, Y.; Reid, J.; Sanchez, R.; Liang, Y.; Paton, B.; Wan, B.-L.; Anthony, N. 2011: Design and synthesis of conformationally constrained inhibitors of non-nucleoside reverse transcriptase. Journal of Medicinal Chemistry 54(22): 7920-7933
Rebolledo, C.L.; Sotelo-Hitschfeld, P.; Brauchi, S.án.; Olavarría, M.Z.ár. 2013: Design and synthesis of conformationally restricted capsaicin analogues based in the 1, 3, 4-thiadiazole heterocycle reveal a novel family of transient receptor potential vanilloid 1 (TRPV1) antagonists. European Journal of Medicinal Chemistry 66: 193-203
Brink, M.; Dahlén, A.; Olsson, T.; Polla, M.; Svensson, T. 2014: Design and synthesis of conformationally restricted inhibitors of active thrombin activatable fibrinolysis inhibitor (TAFIa). Bioorganic and Medicinal Chemistry 22(7): 2261-2268
Prieto, G.; Beijer, S.; Smith, M.L.; He, M.; Au, Y.; Wang, Z.; Bruce, D.A.; de Jong, K.P.; Spivey, J.J.; de Jongh, P.E. 2014: Design and synthesis of copper-cobalt catalysts for the selective conversion of synthesis gas to ethanol and higher alcohols. Angewandte Chemie 53(25): 6397-6401
Yang, Y.; Liu, Q.-W.; Shi, Y.; Song, Z.-G.; Jin, Y.-H.; Liu, Z.-Q. 2014: Design and synthesis of coumarin-3-acylamino derivatives to scavenge radicals and to protect DNA. European Journal of Medicinal Chemistry 84: 1-7
Mizukami, S.; Okada, S.; Kimura, S.; Kikuchi, K. 2009: Design and synthesis of coumarin-based Zn(2+) probes for ratiometric fluorescence imaging. Inorganic Chemistry 48(16): 7630-7638
Zhang, X.; Tian, Y.; Li, Z.; Tian, X.; Sun, H.; Liu, H.; Moore, A.; Ran, C. 2013: Design and synthesis of curcumin analogues for in vivo fluorescence imaging and inhibiting copper-induced cross-linking of amyloid beta species in Alzheimer's disease. Journal of the American Chemical Society 135(44): 16397-16409
Tsuzuki, T.; Sakaguchi, N.; Kudoh, T.; Takano, S.; Uehara, M.; Murayama, T.; Sakurai, T.; Hashii, M.; Higashida, H.; Weber, K.; Guse, A.H.; Kameda, T.; Hirokawa, T.; Kumaki, Y.; Potter, B.V.L.; Fukuda, H.; Arisawa, M.; Shuto, S. 2013: Design and synthesis of cyclic ADP-4-thioribose as a stable equivalent of cyclic ADP-ribose, a calcium ion-mobilizing second messenger. Angewandte Chemie 52(26): 6633-6637
Fang, W.-J.; Kulkarni, S.S.; Murray, T.F.; Aldrich, J.V. 2009: Design and synthesis of cyclic arodyn analogues by ring-closing metathesis (RCM) for kappa opioid receptor (KOP) antagonists. Advances in Experimental Medicine and Biology 611: 279-280
Kiefer, L.; Gorojankina, T.; Dauban, P.; Faure, H.él.èn.; Ruat, M.; Dodd, R.H. 2010: Design and synthesis of cyclic sulfonamides and sulfamates as new calcium sensing receptor agonists. Bioorganic and Medicinal Chemistry Letters 20(24): 7483-7487
Gomez-Paloma, L.; Bruno, I.; Cini, E.; Khochbin, S.; Rodriquez, M.; Taddei, M.; Terracciano, S.; Sadoul, K. 2007: Design and synthesis of cyclopeptide analogues of the potent histone deacetylase inhibitor FR235222. Chemmedchem 2(10): 1511-1519
Chen, H.; Li, Y.; Sheng, C.; Lv, Z.; Dong, G.; Wang, T.; Liu, J.; Zhang, M.; Li, L.; Zhang, T.; Geng, D.; Niu, C.; Li, K. 2013: Design and synthesis of cyclopropylamide analogues of combretastatin-A4 as novel microtubule-stabilizing agents. Journal of Medicinal Chemistry 56(3): 685-699
Sun, L.; Veith, J.M.; Pera, P.; Bernacki, R.J.; Ojima, I. 2010: Design and synthesis of de novo cytotoxic alkaloids by mimicking the bioactive conformation of paclitaxel. Bioorganic and Medicinal Chemistry 18(19): 7101-7112
Li, Y.-F.; Morcos, P.A. 2008: Design and synthesis of dendritic molecular transporter that achieves efficient in vivo delivery of morpholino antisense oligo. Bioconjugate Chemistry 19(7): 1464-1470
Madhuri, V.; Kumar, V.A. 2012: Design and synthesis of dephosphono DNA analogues containing 1,2,3-triazole linker and their UV-melting studies with DNA/RNA. Nucleosides Nucleotides and Nucleic Acids 31(2): 97-111
Wang, X-Feng.; Tian, X-Tao.; Ohkoshi, E.; Qin, B.; Liu, Y-Nan.; Wu, P-Chi.; Hour, M-Jen.; Hung, H-Yi.; Qian, K.; Huang, R.; Bastow, K.F.; Janzen, W.P.; Jin, J.; Morris-Natschke, S.L.; Lee, K-Hsiung.; Xie, L. 2012: Design and synthesis of diarylamines and diarylethers as cytotoxic antitumor agents. Bioorganic and Medicinal Chemistry Letters 22(19): 6224-6228
Darout, E.; Robinson, R.P.; McClure, K.F.; Corbett, M.; Li, B.; Shavnya, A.; Andrews, M.P.; Jones, C.S.; Li, Q.; Minich, M.L.; Mascitti, V.; Guimarães, C.R.W.; Munchhof, M.J.; Bahnck, K.B.; Cai, C.; Price, D.A.; Liras, S.; Bonin, P.D.; Cornelius, P.; Wang, R.; Bagdasarian, V.; Sobota, C.P.; Hornby, S.; Masterson, V.M.; Joseph, R.M.; Kalgutkar, A.S.; Chen, Y. 2013: Design and synthesis of diazatricyclodecane agonists of the G-protein-coupled receptor 119. Journal of Medicinal Chemistry 56(1): 301-319
Pettersson, M.; Johnson, D.S.; Subramanyam, C.; Bales, K.R.; am Ende, C.W.; Fish, B.A.; Green, M.E.; Kauffman, G.W.; Lira, R.; Mullins, P.B.; Navaratnam, T.; Sakya, S.M.; Stiff, C.M.; Tran, T.P.; Vetelino, B.C.; Xie, L.; Zhang, L.; Pustilnik, L.R.; Wood, K.M.; O'Donnell, C.J. 2012: Design and synthesis of dihydrobenzofuran amides as orally bioavailable, centrally active γ-secretase modulators. Bioorganic and Medicinal Chemistry Letters 22(8): 2906-2911
Dandu, R.; Zulli, A.L.; Bacon, E.R.; Underiner, T.; Robinson, C.; Chang, H.; Miknyoczki, S.; Grobelny, J.; Ruggeri, B.A.; Yang, S.; Albom, M.S.; Angeles, T.S.; Aimone, L.D.; Hudkins, R.L. 2008: Design and synthesis of dihydroindazolo[5,4-a]pyrrolo[3,4-c]carbazole oximes as potent dual inhibitors of TIE-2 and VEGF-R2 receptor tyrosine kinases. Bioorganic and Medicinal Chemistry Letters 18(6): 1916-1921
Fang, X.; Fang, L.; Gou, S.; Cheng, L. 2013: Design and synthesis of dimethylaminomethyl-substituted curcumin derivatives/analogues: potent antitumor and antioxidant activity, improved stability and aqueous solubility compared with curcumin. Bioorganic and Medicinal Chemistry Letters 23(5): 1297-1301
Abramova, T.V.; Vasileva, S.V.; Koroleva, L.S.; Kasatkina, N.S.; Silnikov, V.N. 2008: Design and synthesis of dinucleotide 5'-triphosphates with expanded functionality. Bioorganic and Medicinal Chemistry 16(20): 9127-9132
Gudasheva, T.A.; Tarasiuk, A.V.; Pomogaĭbo, S.V.; Logvinov, I.O.; Povarnina, P.I.; Antipova, T.A.; Seredenin, S.B. 2012: Design and synthesis of dipeptide mimetics of brain-derived neurotrophic factor. Bioorganicheskaia Khimiia 38(3): 280-290
Guay, D.; Beaulieu, C.; Truchon, J.-F.; Jagadeeswar Reddy, T.; Zamboni, R.; Bayly, C.I.; Methot, N.; Rubin, J.; Ethier, D.; David Percival, M. 2009: Design and synthesis of dipeptidyl nitriles as potent, selective, and reversible inhibitors of cathepsin C. Bioorganic and Medicinal Chemistry Letters 19(18): 5392-5396
Chonan, T.; Tanaka, H.; Yamamoto, D.; Yashiro, M.; Oi, T.; Wakasugi, D.; Ohoka-Sugita, A.; Io, F.; Koretsune, H.; Hiratate, A. 2010: Design and synthesis of disubstituted (4-piperidinyl)-piperazine derivatives as potent acetyl-CoA carboxylase inhibitors. Bioorganic and Medicinal Chemistry Letters 20(13): 3965-3968
Hom, R.K.; Bowers, S.; Sealy, J.M.; Truong, A.P.; Probst, G.D.; Neitzel, M.L.; Neitz, R.J.; Fang, L.; Brogley, L.; Wu, J.; Konradi, A.W.; Sham, H.L.; Tóth, G.; Pan, H.; Yao, N.; Artis, D.R.; Quinn, K.; Sauer, J.-M.; Powell, K.; Ren, Z.; Bard, F.éd.ér.; Yednock, T.A.; Griswold-Prenner, I. 2010: Design and synthesis of disubstituted thiophene and thiazole based inhibitors of JNK. Bioorganic and Medicinal Chemistry Letters 20(24): 7303-7307
Xu, L.; Jiang, Z.; Qing, Q.; Mai, L.; Zhang, Q.; Lieber, C.M. 2013: Design and synthesis of diverse functional kinked nanowire structures for nanoelectronic bioprobes. Nano Letters 13(2): 746-751
Helmy, S.; Oh, S.; Leibfarth, F.A.; Hawker, C.J.; Read de Alaniz, J. 2014: Design and synthesis of donor-acceptor Stenhouse adducts: a visible light photoswitch derived from furfural. Journal of Organic Chemistry 79(23): 11316-11329
Jadhav, T.; Maragani, R.; Misra, R.; Sreeramulu, V.; Rao, D.N.; Mobin, S.M. 2013: Design and synthesis of donor-acceptor pyrazabole derivatives for multiphoton absorption. Dalton Transactions 42(13): 4340-4342
La Buscató, E.; Blöcher, R.é; Lamers, C.; Klingler, F.-M.; Hahn, S.; Steinhilber, D.; Schubert-Zsilavecz, M.; Proschak, E. 2012: Design and synthesis of dual modulators of soluble epoxide hydrolase and peroxisome proliferator-activated receptors. Journal of Medicinal Chemistry 55(23): 10771-10775
Chen, J.-B.; Chern, T.-R.; Wei, T.-T.; Chen, C.-C.; Lin, J.-H.; Fang, J.-M. 2013: Design and synthesis of dual-action inhibitors targeting histone deacetylases and 3-hydroxy-3-methylglutaryl coenzyme a reductase for cancer treatment. Journal of Medicinal Chemistry 56(9): 3645-3655
Chen, H.; Li, M.; Wan, T.; Zheng, Q.; Cheng, M.; Huang, S.; Wang, Y. 2012: Design and synthesis of dual-ligand modified chitosan as a liver targeting vector. Journal of Materials Science. Materials in Medicine 23(2): 431-441
Oh, C.Hyun.; Liu, L.Jin.; Hong, J.Hee. 2010: Design and synthesis of dually branched 5'-norcarbocyclic adenosine phosphonodiester analogue as a new anti-HIV prodrug. Nucleosides Nucleotides and Nucleic Acids 29(10): 721-733
Hsueh, Y.-S.; Savitha, S.; Sadhasivam, S.; Lin, F.-H.; Shieh, M.-J. 2014: Design and synthesis of elastin-like polypeptides for an ideal nerve conduit in peripheral nerve regeneration. Materials Science and Engineering. C Materials for Biological Applications 38: 119-126
Arjmand, F.; Muddassir, M.; Yousuf, I. 2014: Design and synthesis of enantiomeric (R)- and (S)-copper(II) and diorganotin(IV)-based antitumor agents: their in vitro DNA binding profile, cleavage efficiency and cytotoxicity studies. Journal of Photochemistry and Photobiology. B Biology 136: 62-71
Roy, S.; Basak, A. 2010: Design and synthesis of enediyne-based peptide with selective peptide-cleaving activity. Chemical Communications 46(13): 2283-2285
Peixoto, P.A.; Boulangé, A.; Ball, M.; Naudin, B.; Alle, T.; Cosette, P.; Karuso, P.; Franck, X. 2014: Design and synthesis of epicocconone analogues with improved fluorescence properties. Journal of the American Chemical Society 136(43): 15248-15256
Demizu, Y.; Okuhira, K.; Motoi, H.; Ohno, A.; Shoda, T.; Fukuhara, K.; Okuda, H.; Naito, M.; Kurihara, M. 2012: Design and synthesis of estrogen receptor degradation inducer based on a protein knockdown strategy. Bioorganic and Medicinal Chemistry Letters 22(4): 1793-1796
Nakamura, H.; Ueda, N.; Ban, H.S.; Ueno, M.; Tachikawa, S. 2012: Design and synthesis of fluorescence-labeled closo-dodecaborate lipid: its liposome formation and in vivo imaging targeting of tumors for boron neutron capture therapy. Organic and Biomolecular Chemistry 10(7): 1374-1380
De Ornellas, S.; Slattery, J.M.; Edkins, R.M.; Beeby, A.; Baumann, C.G.; Fairlamb, I.J.S. 2015: Design and synthesis of fluorescent 7-deazaadenosine nucleosides containing π-extended diarylacetylene motifs. Organic and Biomolecular Chemistry 13(1): 68-72
Lansdell, M.I.; Burring, D.J.; Hepworth, D.; Strawbridge, M.; Graham, E.; Guyot, T.; Betson, M.S.; Hart, J.D. 2008: Design and synthesis of fluorescent SGLT2 inhibitors. Bioorganic and Medicinal Chemistry Letters 18(18): 4944-4947
Chorell, E.; Pinkner, J.S.; Bengtsson, C.; Edvinsson, S.; Cusumano, C.K.; Rosenbaum, E.; Johansson, L.B.Å; Hultgren, S.J.; Almqvist, F. 2012: Design and synthesis of fluorescent pilicides and curlicides: bioactive tools to study bacterial virulence mechanisms. Chemistry 18(15): 4522-4532
Kaneda, M.; Misu, R.; Ohno, H.; Hirasawa, A.; Ieda, N.; Uenoyama, Y.; Tsukamura, H.; Maeda, K.-i.; Oishi, S.; Fujii, N. 2014: Design and synthesis of fluorescent probes for GPR54. Bioorganic and Medicinal Chemistry 22(13): 3325-3330
Ma, Y.; Roy, S.; Kong, X.; Chen, Y.; Liu, D.; Hider, R.C. 2012: Design and synthesis of fluorinated iron chelators for metabolic study and brain uptake. Journal of Medicinal Chemistry 55(5): 2185-2195
Kong, W.-Y.; Chen, X.-F.; Shi, J.; Baloch, S.K.; Qi, J.-L.; Zhu, H.-L.; Wang, X.-M.; Yang, Y.-H. 2013: Design and synthesis of fluoroacylshikonin as an anticancer agent. Chirality 25(11): 757-762
Yen, C.-T.; Nakagawa-Goto, K.; Hwang, T.-L.; Morris-Natschke, S.L.; Bastow, K.F.; Wu, Y.-C.; Lee, K.-H. 2012: Design and synthesis of gambogic acid analogs as potent cytotoxic and anti-inflammatory agents. Bioorganic and Medicinal Chemistry Letters 22(12): 4018-4022
Zhang, K.; Schweizer, F. 2009: Design and synthesis of glucose-templated proline-lysine chimera: polyfunctional amino acid chimera with high prolyl cis amide rotamer population. Carbohydrate Research 344(5): 576-585
Wang, H.; Huang, W.; Orwenyo, J.; Banerjee, A.; Vasta, G.R.; Wang, L.-X. 2013: Design and synthesis of glycoprotein-based multivalent glyco-ligands for influenza hemagglutinin and human galectin-3. Bioorganic and Medicinal Chemistry 21(7): 2037-2044
Norgren, A.S.; Arvidsson, P.I. 2008: Design and synthesis of glycosylated beta3-peptides capable of folding into the 3(14)-helical conformation in water. Journal of Organic Chemistry 73(14): 5272-5278
Adane, L.; Bhagat, S.; Arfeen, M.; Bhatia, S.; Sirawaraporn, R.; Sirawaraporn, W.; Chakraborti, A.K.; Bharatam, P.V. 2014: Design and synthesis of guanylthiourea derivatives as potential inhibitors of Plasmodium falciparum dihydrofolate reductase enzyme. Bioorganic and Medicinal Chemistry Letters 24(2): 613-617
Misra, A.; Kumar, P.; Gupta, K.C. 2007: Design and synthesis of hairpin probe for specific mis-match discrimination. Nucleic Acids Symposium Series 51: 311-312
Pawar, V.U.; Ghosh, S.; Chopade, B.A.; Shinde, V.S. 2010: Design and synthesis of harzialactone analogues: promising anticancer agents. Bioorganic and Medicinal Chemistry Letters 20(24): 7243-7245
Chow, C.-F.; Lam, M.H.W.; Wong, W.-Y. 2013: Design and synthesis of heterobimetallic Ru(II)-Ln(III) complexes as chemodosimetric ensembles for the detection of biogenic amine odorants. Analytical Chemistry 85(17): 8246-8253
Arjmand, F.; Muddassir, M. 2010: Design and synthesis of heterobimetallic topoisomerase i and Ii inhibitor complexes: in vitro DNA binding, interaction with 5'-GMP and 5'-TMP and cleavage studies. Journal of Photochemistry and Photobiology. B Biology 101(1): 37-46
Chai, Y.; Paul, A.; Rettig, M.; Wilson, W.D.; Boykin, D.W. 2014: Design and synthesis of heterocyclic cations for specific DNA recognition: from AT-rich to mixed-base-pair DNA sequences. Journal of Organic Chemistry 79(3): 852-866
Hou, Y.; Cheng, Y.; Hobson, T.; Liu, J. 2010: Design and synthesis of hierarchical MnO2 nanospheres/carbon nanotubes/conducting polymer ternary composite for high performance electrochemical electrodes. Nano Letters 10(7): 2727-2733
Rackham, M.D.; Brannigan, J.A.; Rangachari, K.; Meister, S.; Wilkinson, A.J.; Holder, A.A.; Leatherbarrow, R.J.; Tate, E.W. 2014: Design and synthesis of high affinity inhibitors of Plasmodium falciparum and Plasmodium vivax N-myristoyltransferases directed by ligand efficiency dependent lipophilicity (LELP). Journal of Medicinal Chemistry 57(6): 2773-2788
Sarkar, D.; Mandal, M.; Mandal, K. 2013: Design and synthesis of high performance multifunctional ultrathin hematite nanoribbons. Acs Applied Materials and Interfaces 5(22): 11995-12004
Maric, H.M.; Kasaragod, V.B.; Haugaard-Kedström, L.; Hausrat, T.J.; Kneussel, M.; Schindelin, H.; Strømgaard, K. 2015: Design and synthesis of high-affinity dimeric inhibitors targeting the interactions between gephyrin and inhibitory neurotransmitter receptors. Angewandte Chemie 54(2): 490-494
Ogata, M.; Yano, M.; Umemura, S.; Murata, T.; Park, E.Y.; Kobayashi, Y.; Asai, T.; Oku, N.; Nakamura, N.; Matsuo, I.; Usui, T. 2012: Design and synthesis of high-avidity tetravalent glycoclusters as probes for Sambucus sieboldiana agglutinin and characterization of their binding properties. Bioconjugate Chemistry 23(1): 97-105
Fang, Z.; Gu, Z.; Zhu, W.; Zhong, X. 2009: Design and synthesis of high-quality CdS/ZnSe type-Ii core/shell nanocrystals. Journal of Nanoscience and Nanotechnology 9(10): 5880-5886
Zhang, W.; Chen, G.; Wang, J.; Ye, B.-C.; Zhong, X. 2009: Design and synthesis of highly luminescent near-infrared-emitting water-soluble CdTe/CdSe/ZnS core/shell/shell quantum dots. Inorganic Chemistry 48(20): 9723-9731
Bojinov, V.B.; Georgiev, N.I.; Bosch, P. 2009: Design and synthesis of highly photostable yellow-green emitting 1,8-naphthalimides as fluorescent sensors for metal cations and protons. Journal of Fluorescence 19(1): 127-139
Qiu, X.; Zhao, G.-D.; Tang, L.-Q.; Liu, Z.-P. 2014: Design and synthesis of highly potent HIV-1 protease inhibitors with novel isosorbide-derived P2 ligands. Bioorganic and Medicinal Chemistry Letters 24(11): 2465-2468
Zheng, K.; Iqbal, S.; Hernandez, P.; Park, H.; LoGrasso, P.V.; Feng, Y. 2014: Design and synthesis of highly potent and isoform selective JNK3 inhibitors: SAR studies on aminopyrazole derivatives. Journal of Medicinal Chemistry 57(23): 10013-10030
Bach, A.; Chi, C.N.; Pang, G.F.; Olsen, L.; Kristensen, A.S.; Jemth, P.; Strømgaard, K. 2009: Design and synthesis of highly potent and plasma-stable dimeric inhibitors of the PSD-95-NMDA receptor interaction. Angewandte Chemie 48(51): 9685-9689
Taylor, M.T.; Blackman, M.L.; Dmitrenko, O.; Fox, J.M. 2011: Design and synthesis of highly reactive dienophiles for the tetrazine-trans-cyclooctene ligation. Journal of the American Chemical Society 133(25): 9646-9649
Bowers, S.; Truong, A.P.; Ye, M.; Aubele, D.L.; Sealy, J.M.; Neitz, R.J.; Hom, R.K.; Chan, W.; Dappen, M.S.; Galemmo, R.A.; Konradi, A.W.; Sham, H.L.; Zhu, Y.L.; Beroza, P.; Tonn, G.; Zhang, H.; Hoffman, J.; Motter, R.; Fauss, D.; Tanaka, P.; Bova, M.P.; Ren, Z.; Tam, D.; Ruslim, L.; Baker, J.; Pandya, D.; Diep, L.; Fitzgerald, K.; Artis, D.R.; Anderson, J.P.; Bergeron, M. 2013: Design and synthesis of highly selective, orally active Polo-like kinase-2 (Plk-2) inhibitors. Bioorganic and Medicinal Chemistry Letters 23(9): 2743-2749
Fujikawa, Y.; Urano, Y.; Komatsu, T.; Hanaoka, K.; Kojima, H.; Terai, T.; Inoue, H.; Nagano, T. 2008: Design and synthesis of highly sensitive fluorogenic substrates for glutathione S-transferase and application for activity imaging in living cells. Journal of the American Chemical Society 130(44): 14533-14543
Matsumoto, K.; Takahashi, N.; Suzuki, A.; Morii, T.; Saito, Y.; Saito, I. 2011: Design and synthesis of highly solvatochromic fluorescent 2'-deoxyguanosine and 2'-deoxyadenosine analogs. Bioorganic and Medicinal Chemistry Letters 21(4): 1275-1278
Singh, S.; Prasad, N.R.; Chufan, E.E.; Patel, B.A.; Wang, Y.-J.; Chen, Z.-S.; Ambudkar, S.V.; Talele, T.T. 2014: Design and synthesis of human ABCB1 (P-glycoprotein) inhibitors by peptide coupling of diverse chemical scaffolds on carboxyl and amino termini of (S)-valine-derived thiazole amino acid. Journal of Medicinal Chemistry 57(10): 4058-4072
Cagnoni, A.J.; Kovensky, J.é; Uhrig, M.ía.L. 2014: Design and synthesis of hydrolytically stable multivalent ligands bearing thiodigalactoside analogues for peanut lectin and human galectin-3 binding. Journal of Organic Chemistry 79(14): 6456-6467
Sadakiyo, M.; Kasai, H.; Kato, K.; Takata, M.; Yamauchi, M. 2014: Design and synthesis of hydroxide ion-conductive metal-organic frameworks based on salt inclusion. Journal of the American Chemical Society 136(5): 1702-1705
Ng, R.A.; Sun, M.; Bowers, S.; Hom, R.K.; Probst, G.D.; John, V.; Fang, L.Y.; Maillard, M.; Gailunas, A.; Brogley, L.; Neitz, R.J.; Tung, J.S.; Pleiss, M.A.; Konradi, A.W.; Sham, H.L.; Dappen, M.S.; Adler, M.; Yao, N.; Zmolek, W.; Nakamura, D.; Quinn, K.P.; Sauer, J.-M.; Bova, M.P.; Ruslim, L.; Artis, D.R.; Yednock, T.A. 2013: Design and synthesis of hydroxyethylamine (HEA) BACE-1 inhibitors: prime side chromane-containing inhibitors. Bioorganic and Medicinal Chemistry Letters 23(16): 4674-4679
Probst, G.D.; Bowers, S.; Sealy, J.M.; Stupi, B.; Dressen, D.; Jagodzinska, B.M.; Aquino, J.; Gailunas, A.; Truong, A.P.; Tso, L.; Xu, Y.-Z.; Hom, R.K.; John, V.; Tung, J.S.; Pleiss, M.A.; Tucker, J.A.; Konradi, A.W.; Sham, H.L.; Jagodzinski, J.; Toth, G.; Brecht, E.; Yao, N.; Pan, H.; Lin, M.; Artis, D.R.; Ruslim, L.; Bova, M.P.; Sinha, S.; Yednock, T.A.; Gauby, S.; Zmolek, W.; Quinn, K.P.; Sauer, J.-M. 2010: Design and synthesis of hydroxyethylamine (HEA) BACE-1 inhibitors: structure-activity relationship of the aryl region. Bioorganic and Medicinal Chemistry Letters 20(20): 6034-6039
Li, D.-F.; Hu, P.-P.; Liu, M.-S.; Kong, X.-L.; Zhang, J.-C.; Hider, R.C.; Zhou, T. 2013: Design and synthesis of hydroxypyridinone-L-phenylalanine conjugates as potential tyrosinase inhibitors. Journal of Agricultural and Food Chemistry 61(27): 6597-6603
Huang, S.; Qing, J.; Wang, S.; Wang, H.; Zhang, L.; Tang, Y. 2014: Design and synthesis of imidazo[1,2-α][1,8]naphthyridine derivatives as anti-HCV agents via direct C-H arylation. Organic and Biomolecular Chemistry 12(15): 2344-2348
Kamal, A.; Balakrishna, M.; Nayak, V.L.; Shaik, T.B.; Faazil, S.; Nimbarte, V.D. 2014: Design and synthesis of imidazo[2,1-b]thiazole-chalcone conjugates: microtubule-destabilizing agents. Chemmedchem 9(12): 2766-2780
Wang, K.; Xu, W.; Liu, Y.; Zhang, W.; Wang, W.; Shen, J.; Wang, Y. 2013: Design and synthesis of imidazole and triazole derivatives as Lp-PLA₂ inhibitors and the unexpected discovery of highly potent quaternary ammonium salts. Bioorganic and Medicinal Chemistry Letters 23(5): 1187-1192
Ma, Y.; Sun, S.-X.; Cheng, X.-C.; Wang, S.-Q.; Dong, W.-L.; Wang, R.-L.; Xu, W.-R. 2013: Design and synthesis of imidazolidine-2,4-dione derivatives as selective inhibitors by targeting protein tyrosine phosphatase-1B over T-cell protein tyrosine phosphatase. Chemical Biology and Drug Design 82(5): 595-602
Kim, O.; Jeong, Y.; Lee, H.; Hong, S.-S.; Hong, S. 2011: Design and synthesis of imidazopyridine analogues as inhibitors of phosphoinositide 3-kinase signaling and angiogenesis. Journal of Medicinal Chemistry 54(7): 2455-2466
Huang, T.; Zhu, Y.-l.; Dai, X.-q.; Zhang, Q.; Huang, Y. 2011: Design and synthesis of imine compound for metal cation logical gates recognition and setup of double-control fluorescent molecule switch. Guang Pu Xue Yu Guang Pu Fen Xi 31(7): 1834-1837
Shen, Y.-D.; Zhang, S.-W.; Lei, H.-T.; Wang, H.; Xiao, Z.-L.; Jiang, Y.-M.; Sun, Y.-M. 2008: Design and synthesis of immunoconjugates and development of an indirect ELISA for rapid detection of 3, 5-dinitrosalicyclic Acid hydrazide. Molecules 13(9): 2238-2248
Sathe, M.; Merwyn, S.; Ghorpade, R.; Agarwal, G.S.; Rao, M.K.; Rai, G.P.; Kaushik, M.P. 2011: Design and synthesis of immunoconjugates and development of competition inhibition enzyme-linked immunosorbent assay (CIEIA) for the detection of O-isopropyl methylphosphonofluoridate (sarin): an organophosphorous toxicant. Journal of Hazardous Materials 192(3): 1720-1728
Kang, I.-J.; Wang, L.-W.; Hsu, S.-J.; Lee, C.-C.; Lee, Y.-C.; Wu, Y.-S.; Hsu, T.-A.; Yueh, A.; Chao, Y.-S.; Chern, J.-H. 2009: Design and synthesis of indole, 2,3-dihydro-indole, and 3,4-dihydro-2H-quinoline-1-carbothioic acid amide derivatives as novel HCV inhibitors. Bioorganic and Medicinal Chemistry Letters 19(15): 4134-4138
Arisawa, M.; Kasaya, Y.; Obata, T.; Sasaki, T.; Nakamura, T.; Araki, T.; Yamamoto, K.; Sasaki, A.; Yamano, A.; Ito, M.; Abe, H.; Ito, Y.; Shuto, S. 2012: Design and synthesis of indomethacin analogues that inhibit P-glycoprotein and/or multidrug resistant protein without COX inhibitory activity. Journal of Medicinal Chemistry 55(18): 8152-8163
Millan, D.S.; Bunnage, M.E.; Burrows, J.L.; Butcher, K.J.; Dodd, P.G.; Evans, T.J.; Fairman, D.A.; Hughes, S.J.; Kilty, I.C.; Lemaitre, A.; Lewthwaite, R.A.; Mahnke, A.; Mathias, J.P.; Philip, J.; Smith, R.T.; Stefaniak, M.H.; Yeadon, M.; Phillips, C. 2011: Design and synthesis of inhaled p38 inhibitors for the treatment of chronic obstructive pulmonary disease. Journal of Medicinal Chemistry 54(22): 7797-7814
Winkler, J.D.; Isaacs, A.é; Holderbaum, L.; Tatard, V.ér.; Dahmane, N. 2009: Design and synthesis of inhibitors of Hedgehog signaling based on the alkaloid cyclopamine. Organic Letters 11(13): 2824-2827
Yu, Z.; Brannigan, J.A.; Moss, D.K.; Brzozowski, A.Marek.; Wilkinson, A.J.; Holder, A.A.; Tate, E.W.; Leatherbarrow, R.J. 2012: Design and synthesis of inhibitors of Plasmodium falciparum N-myristoyltransferase, a promising target for antimalarial drug discovery. Journal of Medicinal Chemistry 55(20): 8879-8890
Dou, D.; Mandadapu, S.R.; Alliston, K.R.; Kim, Y.; Chang, K.-O.; Groutas, W.C. 2011: Design and synthesis of inhibitors of noroviruses by scaffold hopping. Bioorganic and Medicinal Chemistry 19(19): 5749-5755
Geotti-Bianchini, P.; Beyrath, J.; Chaloin, O.; Formaggio, F.; Bianco, A. 2008: Design and synthesis of intrinsically cell-penetrating nucleopeptides. Organic and Biomolecular Chemistry 6(20): 3661-3663
Hsieh, C.-H.; Wu, F.-I.; Fan, C.-H.; Huang, M.-J.; Lu, K.-Y.; Chou, P.-Y.; Yang, Y.-H.O.; Wu, S.-H.; Chen, I.-C.; Chou, S.-H.; Wong, K.-T.; Cheng, C.-H. 2011: Design and synthesis of iridium bis(carbene) complexes for efficient blue electrophosphorescence. Chemistry 17(33): 9180-9187
Roqué Rosell, N.úr.R.; Mokhlesi, L.; Milton, N.E.; Sweeney, T.R.; Zunszain, P.A.; Curry, S.; Leatherbarrow, R.J. 2014: Design and synthesis of irreversible inhibitors of foot-and-mouth disease virus 3C protease. Bioorganic and Medicinal Chemistry Letters 24(2): 490-494
Ito, H.; Kato, T.; Sawamura, M. 2007: Design and synthesis of isocyanide ligands for catalysis: application to Rh-catalyzed hydrosilylation of ketones. Chemistry An Asian Journal 2(11): 1436-1446
Lavieri, R.; Scott, S.A.; Lewis, J.A.; Selvy, P.E.; Armstrong, M.D.; Alex Brown, H.; Lindsley, C.W. 2009: Design and synthesis of isoform-selective phospholipase D (PLD) inhibitors. Part II. Identification of the 1,3,8-triazaspiro[4,5]decan-4-one privileged structure that engenders PLD2 selectivity. Bioorganic and Medicinal Chemistry Letters 19(8): 2240-2243
Yoshimura, Y.; Asami, K.; Imamichi, T.; Okuda, T.; Shiraki, K.; Takahata, H. 2010: Design and synthesis of isonucleosides constructed on a 2-oxa-6-thiabicyclo[3.2.0]heptane scaffold. Journal of Organic Chemistry 75(12): 4161-4171
Buchstaller, H.-P.; Burgdorf, L.; Finsinger, D.; Stieber, F.; Sirrenberg, C.; Amendt, C.; Grell, M.; Zenke, F.; Krier, M. 2011: Design and synthesis of isoquinolines and benzimidazoles as RAF kinase inhibitors. Bioorganic and Medicinal Chemistry Letters 21(8): 2264-2269
Khaybullin, R.N.; Zhang, M.; Fu, J.; Liang, X.; Li, T.; Katritzky, A.R.; Okunieff, P.; Qi, X. 2014: Design and synthesis of isosteviol triazole conjugates for cancer therapy. Molecules 19(11): 18676-18689
Barnes-Seeman, D.; Boiselle, C.; Capacci-Daniel, C.; Chopra, R.; Hoffmaster, K.; Jones, C.T.; Kato, M.; Lin, K.; Ma, S.; Pan, G.; Shu, L.; Wang, J.; Whiteman, L.; Xu, M.; Zheng, R.; Fu, J. 2014: Design and synthesis of lactam-thiophene carboxylic acids as potent hepatitis C virus polymerase inhibitors. Bioorganic and Medicinal Chemistry Letters 24(16): 3979-3985
Ohta, T.; Fukuda, T.; Ishibashi, F.; Iwao, M. 2009: Design and synthesis of lamellarin D analogues targeting topoisomerase i. Journal of Organic Chemistry 74(21): 8143-8153
An, P.; Yu, Z.; Lin, Q. 2013: Design and synthesis of laser-activatable tetrazoles for a fast and fluorogenic red-emitting 1,3-dipolar cycloaddition reaction. Organic Letters 15(21): 5496-5499
Tateishi, H.; Anraku, K.; Koga, R.; Okamoto, Y.; Fujita, M.; Otsuka, M. 2014: Design and synthesis of lipid-coupled inositol 1,2,3,4,5,6-hexakisphosphate derivatives exhibiting high-affinity binding for the HIV-1 MA domain. Organic and Biomolecular Chemistry 12(27): 5006-5022
Liang, X.; Li, X.; Jing, L.; Xue, P.; Jiang, L.; Ren, Q.; Dai, Z. 2013: Design and synthesis of lipidic organoalkoxysilanes for the self-assembly of liposomal nanohybrid cerasomes with controlled drug release properties. Chemistry 19(47): 16113-16121
Osornio, Y.M.; Uebelhart, P.; Bosshard, S.; Konrad, F.; Siegel, J.S.; Landau, E.M. 2012: Design and synthesis of lipids for the fabrication of functional lipidic cubic-phase biomaterials. Journal of Organic Chemistry 77(23): 10583-10595
Millan, D.S.; Ballard, S.A.; Chunn, S.; Dybowski, J.A.; Fulton, C.K.; Glossop, P.A.; Guillabert, E.; Hewson, C.A.; Jones, R.M.; Lamb, D.J.; Napier, C.M.; Payne-Cook, T.A.; Renery, E.R.; Selby, M.D.; Tutt, M.F.; Yeadon, M. 2011: Design and synthesis of long acting inhaled corticosteroids for the treatment of asthma. Bioorganic and Medicinal Chemistry Letters 21(19): 5826-5830
He, X.; Zhu, N.; Yam, V.W.-W. 2011: Design and synthesis of luminescence chemosensors based on alkynyl phosphine gold(I)-copper(I) aggregates. Dalton Transactions 40(38): 9703-9710
Khan, M.F.; Maurya, C.K.; Dev, K.; Arha, D.; Rai, A.K.; Tamrakar, A.K.; Maurya, R. 2014: Design and synthesis of lupeol analogues and their glucose uptake stimulatory effect in L6 skeletal muscle cells. Bioorganic and Medicinal Chemistry Letters 24(12): 2674-2679
Hanessian, S.; Larsson, A.; Fex, T.; Knecht, W.; Blomberg, N. 2010: Design and synthesis of macrocyclic indoles targeting blood coagulation cascade Factor XIa. Bioorganic and Medicinal Chemistry Letters 20(23): 6925-6928
Xiao, B.; Yin, J.; Park, M.; Liu, J.; Li, J.Lin.; Kim, E.La.; Hong, J.; Chung, H.Young.; Jung, J.H. 2012: Design and synthesis of marine fungal phthalide derivatives as PPAR-γ agonists. Bioorganic and Medicinal Chemistry 20(16): 4954-4961
Majik, M.S.; Rodrigues, C.; Mascarenhas, S.; D'Souza, L. 2014: Design and synthesis of marine natural product-based 1H-indole-2,3-dione scaffold as a new antifouling/antibacterial agent against fouling bacteria. Bioorganic Chemistry 54: 89-95
Brown, N.; Gao, G.; Minatoya, M.; Xie, B.; Vandervelde, D.; Lushington, G.H.; Perchellet, J.-P.H.; Perchellet, E.M.; Crow, K.R.; Buszek, K.R. 2008: Design and synthesis of medium-ring lactam libraries inspired by octalactin a. a convergent-divergent approach. Journal of Combinatorial Chemistry 10(5): 628-631
Oishi, S.; Kodera, Y.; Nishikawa, H.; Kamitani, H.; Watabe, T.; Ohno, H.; Tochikura, T.; Shimane, K.; Kodama, E.; Matsuoka, M.; Mizukoshi, F.; Tsujimoto, H.; Fujii, N. 2009: Design and synthesis of membrane fusion inhibitors against the feline immunodeficiency virus. Bioorganic and Medicinal Chemistry 17(14): 4916-4920
Krishna, P.M.; Reddy, N.B.G.; Kottam, N.; Yallur, B.C.; Katreddi, H.R. 2013: Design and synthesis of metal complexes of (2E)-2-[(2E)-3-phenylprop-2-en-1-ylidene]hydrazinecarbothioamide and their photocatalytic degradation of methylene blue. Thescientificworldjournal 2013: 828313
Tang, T.; Zhang, L.; Fu, W.; Ma, Y.; Xu, J.; Jiang, J.; Fang, G.; Xiao, F.-S. 2013: Design and synthesis of metal sulfide catalysts supported on zeolite nanofiber bundles with unprecedented hydrodesulfurization activities. Journal of the American Chemical Society 135(31): 11437-11440
Perry, J.J.; Perman, J.A.; Zaworotko, M.J. 2009: Design and synthesis of metal-organic frameworks using metal-organic polyhedra as supermolecular building blocks. Chemical Society Reviews 38(5): 1400-1417
Sorto, N.A.; Painter, P.P.; Fettinger, J.C.; Tantillo, D.J.; Shaw, J.T. 2013: Design and synthesis of mimics of the T7-loop of FtsZ. Organic Letters 15(11): 2700-2703
Li, Z.; Hao, P.; Li, L.; Tan, C.Y.J.; Cheng, X.; Chen, G.Y.J.; Sze, S.K.; Shen, H.-M.; Yao, S.Q. 2013: Design and synthesis of minimalist terminal alkyne-containing diazirine photo-crosslinkers and their incorporation into kinase inhibitors for cell- and tissue-based proteome profiling. Angewandte Chemie 52(33): 8551-8556
Perro, A.; Meng, G.; Fung, J.; Manoharan, V.N. 2009: Design and synthesis of model transparent aqueous colloids with optimal scattering properties. Langmuir: the Acs Journal of Surfaces and Colloids 25(19): 11295-11298
Coughlin, J.E.; Henson, Z.B.; Welch, G.C.; Bazan, G.C. 2014: Design and synthesis of molecular donors for solution-processed high-efficiency organic solar cells. Accounts of Chemical Research 47(1): 257-270
Sharma, L.K.; Cupit, P.M.; Goronga, T.; Webb, T.R.; Cunningham, C. 2014: Design and synthesis of molecular probes for the determination of the target of the anthelmintic drug praziquantel. Bioorganic and Medicinal Chemistry Letters 24(11): 2469-2472
Mehdinia, A.; Aziz-Zanjani, M.O.; Ahmadifar, M.; Jabbari, A. 2013: Design and synthesis of molecularly imprinted polypyrrole based on nanoreactor SBA-15 for recognition of ascorbic acid. Biosensors and Bioelectronics 39(1): 88-93
Hoque, M.A.; Islam, M.S.; Islam, M.N.; Kato, T.; Nishino, N.; Ito, A.; Yoshida, M. 2014: Design and synthesis of mono and bicyclic tetrapeptides thioester as potent inhibitor of histone deacetylases. Amino Acids 46(10): 2435-2444
Traina, C.A.; Bakus, R.C.; Bazan, G.C. 2011: Design and synthesis of monofunctionalized, water-soluble conjugated polymers for biosensing and imaging applications. Journal of the American Chemical Society 133(32): 12600-12607
Fish, P.V.; Deur, C.; Gan, X.; Greene, K.; Hoople, D.; Mackenny, M.; Para, K.S.; Reeves, K.; Ryckmans, T.; Stiff, C.; Stobie, A.; Wakenhut, F.; Whitlock, G.A. 2008: Design and synthesis of morpholine derivatives. SAR for dual serotonin and noradrenaline reuptake inhibition. Bioorganic and Medicinal Chemistry Letters 18(8): 2562-2566
Brinãs, R.P.; Sundgren, A.; Sahoo, P.; Morey, S.; Rittenhouse-Olson, K.; Wilding, G.E.; Deng, W.; Barchi, J.J. 2012: Design and synthesis of multifunctional gold nanoparticles bearing tumor-associated glycopeptide antigens as potential cancer vaccines. Bioconjugate Chemistry 23(8): 1513-1523
Ding, F.; Ji, L.; William, R.; Chai, H.; Liu, X.-W. 2014: Design and synthesis of multivalent neoglycoconjugates by click conjugations. Beilstein Journal of Organic Chemistry 10: 1325-1332
Leclerc, V.ér.; Ettaoussi, M.; Rami, M.; Farce, A.; Boutin, J.A.; Delagrange, P.; Caignard, D.-H.; Renard, P.; Berthelot, P.; Yous, S.ïd. 2011: Design and synthesis of naphthalenic derivatives as new ligands at the melatonin binding site MT3. European Journal of Medicinal Chemistry 46(5): 1622-1629
Xu, K.; Xiao, Z.; Tang, Y.B.; Huang, L.; Chen, C.-H.; Ohkoshi, E.; Lee, K.-H. 2012: Design and synthesis of naphthoquinone derivatives as antiproliferative agents and 20S proteasome inhibitors. Bioorganic and Medicinal Chemistry Letters 22(8): 2772-2774
Qin, Z.; Luo, J.; VandeVrede, L.; Tavassoli, E.; Fa', M.; Teich, A.F.; Arancio, O.; Thatcher, G.R.J. 2012: Design and synthesis of neuroprotective methylthiazoles and modification as NO-chimeras for neurodegenerative therapy. Journal of Medicinal Chemistry 55(15): 6784-6801
Carvalho, S.A.; Feitosa, L.O.; Soares, M.ár.; Costa, T.E.M.M.; Henriques, M.G.; Salomão, K.; de Castro, S.L.; Kaiser, M.; Brun, R.; Wardell, J.L.; Wardell, S.M.S.V.; Trossini, G.H.G.; Andricopulo, A.D.; da Silva, E.F.; Fraga, C.A.M. 2012: Design and synthesis of new (E)-cinnamic N-acylhydrazones as potent antitrypanosomal agents. European Journal of Medicinal Chemistry 54: 512-521
Zarghi, A.; Zebardast, T.; Hajighasemali, F.; Alipoor, E.; Daraie, B.; Hedayati, M. 2012: Design and synthesis of new 1,3-benzdiazinan-4-one derivatives as selective cyclooxygenase (COX-2) inhibitors. Archiv der Pharmazie 345(4): 257-264
Zarghi, A.; Zebardast, T.; Daraie, B.; Hedayati, M. 2009: Design and synthesis of new 1,3-benzthiazinan-4-one derivatives as selective cyclooxygenase (COX-2) inhibitors. Bioorganic and Medicinal Chemistry 17(15): 5369-5373
Iman, M.; Davood, A.; Nematollahi, A.R.; Dehpoor, A.R.; Shafiee, A. 2011: Design and synthesis of new 1,4-dihydropyridines containing 4(5)-chloro-5(4)-imidazolyl substituent as a novel calcium channel blocker. Archives of Pharmacal Research 34(9): 1417-1426
Zhang, R.; Gong, Q.; Emge, T.J.; Banerjee, D.; Li, J. 2013: Design and synthesis of new 1D and 2D R-isophthalic acid-based coordination polymers (R = hydrogen or bromine). Chimia 67(6): 393-396
Abdel-Wahab, B.F.; Abdel-Latif, E.; Mohamed, H.A.; Awad, G.E.A. 2012: Design and synthesis of new 4-pyrazolin-3-yl-1,2,3-triazoles and 1,2,3-triazol-4-yl-pyrazolin-1-ylthiazoles as potential antimicrobial agents. European Journal of Medicinal Chemistry 52: 263-268
Zhao, X.-B.; Goto, M.; Song, Z.-L.; Morris-Natschke, S.L.; Zhao, Y.; Wu, D.; Yang, L.; Li, S.-G.; Liu, Y.-Q.; Zhu, G.-X.; Wu, X.-B.; Lee, K.-H. 2014: Design and synthesis of new 7-(N-substituted-methyl)-camptothecin derivatives as potent cytotoxic agents. Bioorganic and Medicinal Chemistry Letters 24(16): 3850-3853
Hayallah, A.K.M.; Talhouni, A.A.; Alim, A.A.M.A. 2012: Design and synthesis of new 8-anilide theophylline derivatives as bronchodilators and antibacterial agents. Archives of Pharmacal Research 35(8): 1355-1368
Boechat, N.; Pinheiro, L.C.S.; Santos-Filho, O.A.; Silva, I.C. 2011: Design and synthesis of new N-(5-trifluoromethyl)-1H-1,2,4-triazol-3-yl benzenesulfonamides as possible antimalarial prototypes. Molecules 16(9): 8083-8097
Yen, C.-T.; Hwang, T.-L.; Wu, Y.-C.; Hsieh, P.-W. 2009: Design and synthesis of new N-(fluorenyl-9-methoxycarbonyl) (Fmoc)-dipeptides as anti-inflammatory agents. European Journal of Medicinal Chemistry 44(5): 1933-1940
Tsotinis, A.; Gourgourinis, J.; Eleutheriades, A.; Davidson, K.; Sugden, D. 2007: Design and synthesis of new N-OMe fluoro-indole melatoninergics. Medicinal Chemistry 3(6): 561-571
Jiang, M.; Tang, D.; Zhao, X.; Li, Q.; Zhuang, Y.; Wei, X.; Li, X.; Liu, Y.; Wu, X-Yan.; Shao, Z.; Gong, B.; Shen, Y-Mei. 2014: Design and synthesis of new acid cleavable linkers for DNA sequencing by synthesis. Nucleosides Nucleotides and Nucleic Acids 33(12): 774-785
Papanastasiou, I.; Prousis, K.C.; Georgikopoulou, K.; Pavlidis, T.; Scoulica, E.; Kolocouris, N.; Calogeropoulou, T. 2010: Design and synthesis of new adamantyl-substituted antileishmanial ether phospholipids. Bioorganic and Medicinal Chemistry Letters 20(18): 5484-5487
Liu, Y.; Yu, H.; Zhao, L.; Zhang, H. 2013: Design and synthesis of new agents for neuronal nicotinic acetylcholine receptor (nAChRs) imaging. Nuclear Medicine and Biology 40(1): 126-134
Ganesan, M.; Madhukarrao, R.V.; Ramesh, N.G. 2010: Design and synthesis of new amino-modified iminocyclitols: selective inhibitors of alpha-galactosidase. Organic and Biomolecular Chemistry 8(7): 1527-1530
El-Deeb, I.M.; Lee, S.H. 2010: Design and synthesis of new anticancer pyrimidines with multiple-kinase inhibitory effect. Bioorganic and Medicinal Chemistry 18(11): 3860-3874
Le Roux, A.; Kuzmanovski, I.; Habrant, D.; Meunier, S.ép.; Bischoff, P.; Nadal, B.; Thetiot-Laurent, S.A.-L.; Le Gall, T.; Wagner, A.; Novič, M. 2011: Design and synthesis of new antioxidants predicted by the model developed on a set of pulvinic acid derivatives. Journal of Chemical Information and Modeling 51(12): 3050-3059
Maji, B.; Kumar, K.; Kaulage, M.; Muniyappa, K.; Bhattacharya, S. 2014: Design and synthesis of new benzimidazole-carbazole conjugates for the stabilization of human telomeric DNA, telomerase inhibition, and their selective action on cancer cells. Journal of Medicinal Chemistry 57(16): 6973-6988
Prezzavento, O.; Arena, E.; Parenti, C.; Pasquinucci, L.; Aricò, G.; Scoto, G.M.; Grancara, S.; Toninello, A.; Ronsisvalle, S. 2013: Design and synthesis of new bifunctional sigma-1 selective ligands with antioxidant activity. Journal of Medicinal Chemistry 56(6): 2447-2455
Barve, I.J.; Chen, C.-Y.; Salunke, D.B.; Chung, W.-S.; Sun, C.-M. 2012: Design and synthesis of new biprivileged molecular scaffolds: indolo-fused benzodiazepinyl/quinoxalinyl benzimidazoles. Chemistry An Asian Journal 7(7): 1684-1690
Da Silva, G.D.; da Silva, M.G.; Souza, E.M.P.V.E.; Barison, A.; Simões, S.C.; Varotti, F.P.; Barbosa, L.A.; Viana, G.H.R.; Villar, J.é A.F.P. 2012: Design and synthesis of new chacones substituted with azide/triazole groups and analysis of their cytotoxicity towards Hela cells. Molecules 17(9): 10331-10343
Shintani, R.; Narui, R.; Tsutsumi, Y.; Hayashi, S.; Hayashi, T. 2011: Design and synthesis of new chiral phosphorus-olefin bidentate ligands and their use in the rhodium-catalyzed asymmetric addition of organoboroxines to N-sulfonyl imines. Chemical Communications 47(21): 6123-6125
Radwan, A.A.; Alanazi, F.K. 2014: Design and synthesis of new cholesterol-conjugated 5-Fluorouracil: a novel potential delivery system for cancer treatment. Molecules 19(9): 13177-13187
Kotera, N.; Delacour, L.éa.; Traoré, T.én.; Tassali, N.; Berthault, P.; Buisson, D.-A.; Dognon, J.-P.; Rousseau, B. 2011: Design and synthesis of new cryptophanes with intermediate cavity sizes. Organic Letters 13(9): 2153-2155
Suzuki, Y.; Takagi, N.; Chimuro, T.; Shinohara, A.; Sakaguchi, N.; Hiratsuka, A.; Yokoyama, K. 2011: Design and synthesis of new fluorescent probe for rapid and highly sensitive detection of proteins via electrophoretic gel stain. Electrophoresis 32(12): 1403-1413
Wilson, J.L.; Fayad Kobeissi, S.; Oudir, S.; Haas, B.; Michel, B.; Dubois Randé, J.-L.; Ollivier, A.; Martens, T.; Rivard, M.; Motterlini, R.; Foresti, R. 2014: Design and synthesis of new hybrid molecules that activate the transcription factor Nrf2 and simultaneously release carbon monoxide. Chemistry 20(45): 14698-14704
Kim, J.Jin.; Kim, H.Rae.; Arai, H.; Lee, S.Hyup. 2012: Design and synthesis of new mitomycin dimers containing a seven-membered cyclic disulfide and a diol linkers. Archives of Pharmacal Research 35(8): 1413-1420
Malik, S.; Ahuja, P.; Sahu, K.; Khan, S.A. 2014: Design and synthesis of new of 3-(benzo[d]isoxazol-3-yl)-1-substituted pyrrolidine-2, 5-dione derivatives as anticonvulsants. European Journal of Medicinal Chemistry 84: 42-50
El-Deeb, I.M.; Lee, S.H. 2010: Design and synthesis of new potent anticancer pyrazoles with high FLT3 kinase inhibitory selectivity. Bioorganic and Medicinal Chemistry 18(11): 3961-3973
Iwahashi, M.; Takahashi, E.; Tanaka, M.; Matsunaga, Y.; Okada, Y.; Matsumoto, R.; Nambu, F.; Nakai, H.; Toda, M. 2011: Design and synthesis of new prostaglandin D₂ receptor antagonists. Bioorganic and Medicinal Chemistry 19(18): 5361-5371
Zarghi, A.; Rao, P.N.P.; Knaus, E.E. 2007: Design and synthesis of new rofecoxib analogs as selective cyclooxygenase-2 (COX-2) inhibitors: replacement of the methanesulfonyl pharmacophore by a N-acetylsulfonamido bioisostere. Journal of Pharmacy and Pharmaceutical Sciences: a Publication of the Canadian Society for Pharmaceutical Sciences Societe Canadienne des Sciences Pharmaceutiques 10(2): 159-167
Rachid, Z.; Macphee, M.; Williams, C.; Todorova, M.; Jean-Claude, B.J. 2009: Design and synthesis of new stabilized combi-triazenes for targeting solid tumors expressing the epidermal growth factor receptor (EGFR) or its closest homologue HER2. Bioorganic and Medicinal Chemistry Letters 19(18): 5505-5509
Tian, Y.; Uchida, K.; Kurata, H.; Hirao, Y.; Nishiuchi, T.; Kubo, T. 2014: Design and synthesis of new stable fluorenyl-based radicals. Journal of the American Chemical Society 136(36): 12784-12793
Foroughinia, F.; Javidnia, K.; Amirghofran, Z.; Mehdipour, A.; Miri, R. 2008: Design and synthesis of new symmetrical derivatives of dihydropyridine containing a pyridyl group on the 3, 5-positions and evaluation of their cytotoxic and multidrug resistance reversal activity. Journal of Pharmacy and Pharmacology 60(11): 1481-1489
Escribano, A.; Mateo, A.I.; Martin de la Nava, E.M.; Mayhugh, D.R.; Cockerham, S.L.; Beyer, T.P.; Schmidt, R.J.; Cao, G.; Zhang, Y.; Jones, T.M.; Borel, A.G.; Sweetana, S.A.; Cannady, E.A.; Mantlo, N.B. 2012: Design and synthesis of new tetrahydroquinolines derivatives as CETP inhibitors. Bioorganic and Medicinal Chemistry Letters 22(11): 3671-3675
De Bona, P.; Giuffrida, M.L.; Caraci, F.; Copani, A.; Pignataro, B.; Attanasio, F.; Cataldo, S.; Pappalardo, G.; Rizzarelli, E. 2009: Design and synthesis of new trehalose-conjugated pentapeptides as inhibitors of Abeta(1-42) fibrillogenesis and toxicity. Journal of Peptide Science: An Official Publication of the European Peptide Society 15(3): 220-228
Konno, S.; Thanigaimalai, P.; Yamamoto, T.; Nakada, K.; Kakiuchi, R.; Takayama, K.; Yamazaki, Y.; Yakushiji, F.; Akaji, K.; Kiso, Y.; Kawasaki, Y.; Chen, S.-E.; Freire, E.; Hayashi, Y. 2013: Design and synthesis of new tripeptide-type SARS-CoV 3CL protease inhibitors containing an electrophilic arylketone moiety. Bioorganic and Medicinal Chemistry 21(2): 412-424
Gu, W.; Chen, B.; Ge, M. 2014: Design and synthesis of new vancomycin derivatives. Bioorganic and Medicinal Chemistry Letters 24(10): 2305-2308
Peng, S.-P.; Yu, L.-P.; Li, J.-Q. 2009: Design and synthesis of nitrogen-containing benzoheterocyclic derivatives and their antipsychotic activities. Yao Xue Xue Bao 44(9): 994-1001
Fujigaya, T.; Uchinoumi, T.; Kaneko, K.; Nakashima, N. 2011: Design and synthesis of nitrogen-containing calcined polymer/carbon nanotube hybrids that act as a platinum-free oxygen reduction fuel cell catalyst. Chemical Communications 47(24): 6843-6845
Subramanian, T.; Ren, H.; Subramanian, K.Leela.; Sunkara, M.; Onono, F.O.; Morris, A.J.; Spielmann, H.Peter. 2014: Design and synthesis of non-hydrolyzable homoisoprenoid α-monofluorophosphonate inhibitors of PPAPDC family integral membrane lipid phosphatases. Bioorganic and Medicinal Chemistry Letters 24(18): 4414-4417
Rawls, K.A.; Grundner, C.; Ellman, J.A. 2010: Design and synthesis of nonpeptidic, small molecule inhibitors for the Mycobacterium tuberculosis protein tyrosine phosphatase PtpB. Organic and Biomolecular Chemistry 8(18): 4066-4070
Fujii, S.; Yamada, A.; Nakano, E.; Takeuchi, Y.; Mori, S.; Masuno, H.; Kagechika, H. 2014: Design and synthesis of nonsteroidal progesterone receptor antagonists based on C,C'-diphenylcarborane scaffold as a hydrophobic pharmacophore. European Journal of Medicinal Chemistry 84: 264-277
Kim, E.; Liu, L.Jin.; Lee, W.; Hong, J.Hee. 2012: Design and synthesis of novel 1',3'-dioxolane 5'-deoxyphosphonic acid purine analogues as potent antiviral agents. Nucleosides Nucleotides and Nucleic Acids 31(2): 85-96
Khazir, J.; Hyder, I.; Gayatri, J.L.; Prasad Yandrati, L.; Nalla, N.; Chasoo, G.; Mahajan, A.; Saxena, A.K.; Alam, M.S.; Qazi, G.N.; Sampath Kumar, H.M. 2014: Design and synthesis of novel 1,2,3-triazole derivatives of coronopilin as anti-cancer compounds. European Journal of Medicinal Chemistry 82: 255-262
Duan, Y.-C.; Ma, Y.-C.; Zhang, E.; Shi, X.-J.; Wang, M.-M.; Ye, X.-W.; Liu, H.-M. 2013: Design and synthesis of novel 1,2,3-triazole-dithiocarbamate hybrids as potential anticancer agents. European Journal of Medicinal Chemistry 62: 11-19
Ma, L.-Y.; Pang, L.-P.; Wang, B.; Zhang, M.; Hu, B.; Xue, D.-Q.; Shao, K.-P.; Zhang, B.-L.; Liu, Y.; Zhang, E.; Liu, H.-M. 2014: Design and synthesis of novel 1,2,3-triazole-pyrimidine hybrids as potential anticancer agents. European Journal of Medicinal Chemistry 86: 368-380
Fujishima, T.; Nozaki, T.; Suenaga, T. 2013: Design and synthesis of novel 1,25-dihydroxyvitamin D3 analogues having a spiro-oxetane fused at the C2 position in the A-ring. Bioorganic and Medicinal Chemistry 21(17): 5209-5217
Mohamed, L.W.; El-Yamany, M.F. 2012: Design and synthesis of novel 1,4-benzodiazepine derivatives and their biological evaluation as cholinesterase inhibitors. Archives of Pharmacal Research 35(8): 1369-1377
Jeong, L.S.; Choi, Y.N.; Tosh, D.K.; Choi, W.J.; Kim, H.O.; Choi, J. 2008: Design and synthesis of novel 2',3'-dideoxy-4'-selenonucleosides as potential antiviral agents. Bioorganic and Medicinal Chemistry 16(23): 9891-9897
Lv, Z.; Zhang, Y.; Zhang, M.; Chen, H.; Sun, Z.; Geng, D.; Niu, C.; Li, K. 2013: Design and synthesis of novel 2'-hydroxy group substituted 2-pyridone derivatives as anticancer agents. European Journal of Medicinal Chemistry 67: 447-453
Alagarsamy, V.; Parthiban, P. 2013: Design and synthesis of novel 2-(3-substituted propyl)-3-(2-methyl phenyl) quinazolin-4-(3H)-ones as a new class of H1-antihistaminic agents. Journal of Enzyme Inhibition and Medicinal Chemistry 28(1): 65-71
Qin, M.; Zhai, X.; Xie, H.; Ma, J.; Lu, K.; Wang, Y.; Wang, L.; Gu, Y.; Gong, P. 2014: Design and synthesis of novel 2-(4-(2-(dimethylamino)ethyl)-4H-1,2,4-triazol-3-yl)pyridines as potential antitumor agents. European Journal of Medicinal Chemistry 81: 47-58
Liu, X.-H.; Jia, Y.-M.; Song, B.-A.; Pang, Z.-x.; Yang, S. 2013: Design and synthesis of novel 2-methyl-4,5-substitutedbenzo[f]-3,3a,4,5-tetrahydro-pyrazolo[1,5-d][1,4]oxazepin-8(7H)-one derivatives as telomerase inhibitors. Bioorganic and Medicinal Chemistry Letters 23(3): 720-723
Bansal, S.; Bala, M.; Suthar, S.K.; Choudhary, S.; Bhattacharya, S.; Bhardwaj, V.; Singla, S.; Joseph, A. 2014: Design and synthesis of novel 2-phenyl-5-(1,3-diphenyl-1H-pyrazol-4-yl)-1,3,4-oxadiazoles as selective COX-2 inhibitors with potent anti-inflammatory activity. European Journal of Medicinal Chemistry 80: 167-174
Chang, S.; Yin, S.-L.; Wang, J.; Jing, Y.-K.; Dong, J.-H. 2009: Design and synthesis of novel 2-phenylaminopyrimidine (PAP) derivatives and their antiproliferative effects in human chronic myeloid leukemia cells. Molecules 14(10): 4166-4179
Verissimo, E.; Berry, N.; Gibbons, P.; Cristiano, M.L.S.; Rosenthal, P.J.; Gut, J.; Ward, S.A.; O'Neill, P.M. 2008: Design and synthesis of novel 2-pyridone peptidomimetic falcipain 2/3 inhibitors. Bioorganic and Medicinal Chemistry Letters 18(14): 4210-4214
Kushwaha, K.; Kaushik, N.; Lata; Jain, S.C. 2014: Design and synthesis of novel 2H-chromen-2-one derivatives bearing 1,2,3-triazole moiety as lead antimicrobials. Bioorganic and Medicinal Chemistry Letters 24(7): 1795-1801
Comes Franchini, M.; Bonini, B.F.; Camaggi, C.M.; Gentili, D.; Pession, A.; Rani, M.; Strocchi, E. 2010: Design and synthesis of novel 3,4-disubstituted pyrazoles for nanomedicine applications against malignant gliomas. European Journal of Medicinal Chemistry 45(5): 2024-2033
Razzaghi-Asl, N.; Firuzi, O.; Hemmateenejad, B.; Javidnia, K.; Edraki, N.; Miri, R. 2013: Design and synthesis of novel 3,5-bis-N-(aryl/heteroaryl) carbamoyl-4-aryl-1,4-dihydropyridines as small molecule BACE-1 inhibitors. Bioorganic and Medicinal Chemistry 21(22): 6893-6909
Cho, S.Y.; Lee, B.H.; Jung, H.; Yun, C.S.; Ha, J.D.; Kim, H.R.; Chae, C.H.; Lee, J.H.; Seo, H.W.; Oh, K.-S. 2013: Design and synthesis of novel 3-(benzo[d]oxazol-2-yl)-5-(1-(piperidin-4-yl)-1H-pyrazol-4-yl)pyridin-2-amine derivatives as selective G-protein-coupled receptor kinase-2 and -5 inhibitors. Bioorganic and Medicinal Chemistry Letters 23(24): 6711-6716
Raval, S.; Raval, P.; Bandyopadhyay, D.; Soni, K.; Yevale, D.; Jogiya, D.; Modi, H.; Joharapurkar, A.; Gandhi, N.; Jain, M.R.; Patel, P.R. 2008: Design and synthesis of novel 3-hydroxy-cyclobut-3-ene-1,2-dione derivatives as thyroid hormone receptor beta (TR-beta) selective ligands. Bioorganic and Medicinal Chemistry Letters 18(14): 3919-3924
Tang, L.; Zhao, L.; Hong, L.; Yang, F.; Sheng, R.; Chen, J.; Shi, Y.; Zhou, N.; Hu, Y. 2013: Design and synthesis of novel 3-substituted-indole derivatives as selective H3 receptor antagonists and potent free radical scavengers. Bioorganic and Medicinal Chemistry 21(19): 5936-5944
Suthar, S.K.; Bansal, S.; Lohan, S.; Modak, V.; Chaudhary, A.; Tiwari, A. 2013: Design and synthesis of novel 4-(4-oxo-2-arylthiazolidin-3-yl)benzenesulfonamides as selective inhibitors of carbonic anhydrase IX over i and Ii with potential anticancer activity. European Journal of Medicinal Chemistry 66: 372-379
Cai, J.; Sun, M.; Wu, X.; Chen, J.; Wang, P.; Zong, X.; Ji, M. 2013: Design and synthesis of novel 4-benzothiazole amino quinazolines Dasatinib derivatives as potential anti-tumor agents. European Journal of Medicinal Chemistry 63: 702-712
Xie, W.; Xie, S.; Zhou, Y.; Tang, X.; Liu, J.; Yang, W.; Qiu, M. 2014: Design and synthesis of novel 5,6-disubstituted pyridine-2,3-dione-3-thiosemicarbazone derivatives as potential anticancer agents. European Journal of Medicinal Chemistry 81: 22-27
Liu, X.-H.; Li, J.; Shi, J.B.; Song, B.-A.; Qi, X.-B. 2012: Design and synthesis of novel 5-phenyl-N-piperidine ethanone containing 4,5-dihydropyrazole derivatives as potential antitumor agents. European Journal of Medicinal Chemistry 51: 294-299
El-Azab, A.S.; Eltahir, K.E.H. 2012: Design and synthesis of novel 7-aminoquinazoline derivatives: antitumor and anticonvulsant activities. Bioorganic and Medicinal Chemistry Letters 22(5): 1879-1885
Li, Z.; Zhou, Z.-L.; Miao, Z.-H.; Lin, L.-P.; Feng, H.-J.; Tong, L.-J.; Ding, J.; Li, Y.-C. 2009: Design and synthesis of novel C14-hydroxyl substituted triptolide derivatives as potential selective antitumor agents. Journal of Medicinal Chemistry 52(16): 5115-5123
Trujillo, J.I.; Huang, W.; Hughes, R.O.; Rogier, D.J.; Turner, S.R.; Devraj, R.; Morton, P.A.; Xue, C.-B.; Chao, G.; Covington, M.B.; Newton, R.C.; Metcalf, B. 2011: Design and synthesis of novel CCR2 antagonists: investigation of non-aryl/heteroaryl binding motifs. Bioorganic and Medicinal Chemistry Letters 21(6): 1827-1831
Zhang, B.-L.; Zhang, E.; Pang, L.-P.; Song, L.-X.; Li, Y.-F.; Yu, B.; Liu, H.-M. 2013: Design and synthesis of novel D-ring fused steroidal heterocycles. Steroids 78(12-13): 1200-1208
Okaniwa, M.; Hirose, M.; Imada, T.; Ohashi, T.; Hayashi, Y.; Miyazaki, T.; Arita, T.; Yabuki, M.; Kakoi, K.; Kato, J.; Takagi, T.; Kawamoto, T.; Yao, S.; Sumita, A.; Tsutsumi, S.; Tottori, T.; Oki, H.; Sang, B.-C.; Yano, J.; Aertgeerts, K.; Yoshida, S.; Ishikawa, T. 2012: Design and synthesis of novel DFG-out RAF/vascular endothelial growth factor receptor 2 (VEGFR2) inhibitors. 1. Exploration of [5,6]-fused bicyclic scaffolds. Journal of Medicinal Chemistry 55(7): 3452-3478
Okaniwa, M.; Imada, T.; Ohashi, T.; Miyazaki, T.; Arita, T.; Yabuki, M.; Sumita, A.; Tsutsumi, S.; Higashikawa, K.; Takagi, T.; Kawamoto, T.; Inui, Y.; Yoshida, S.; Ishikawa, T. 2012: Design and synthesis of novel DFG-out RAF/vascular endothelial growth factor receptor 2 (VEGFR2) inhibitors: 2. Synthesis and characterization of a novel imide-type prodrug for improving oral absorption. Bioorganic and Medicinal Chemistry 20(15): 4680-4692
Hirose, M.; Okaniwa, M.; Miyazaki, T.; Imada, T.; Ohashi, T.; Tanaka, Y.; Arita, T.; Yabuki, M.; Kawamoto, T.; Tsutsumi, S.; Sumita, A.; Takagi, T.; Sang, B.-C.; Yano, J.; Aertgeerts, K.; Yoshida, S.; Ishikawa, T. 2012: Design and synthesis of novel DFG-out RAF/vascular endothelial growth factor receptor 2 (VEGFR2) inhibitors: 3. Evaluation of 5-amino-linked thiazolo[5,4-d]pyrimidine and thiazolo[5,4-b]pyridine derivatives. Bioorganic and Medicinal Chemistry 20(18): 5600-5615
Wu, X.; Li, M.; Qu, Y.; Tang, W.; Zheng, Y.; Lian, J.; Ji, M.; Xu, L. 2010: Design and synthesis of novel Gefitinib analogues with improved anti-tumor activity. Bioorganic and Medicinal Chemistry 18(11): 3812-3822
Frlan, R.; Kovac, A.; Blanot, D.; Gobec, S.; Pecar, S.; Obreza, A. 2008: Design and synthesis of novel N-benzylidenesulfonohydrazide inhibitors of MurC and MurD as potential antibacterial agents. Molecules 13(1): 11-30
Johnson, T.W.; Tanis, S.P.; Butler, S.L.; Dalvie, D.; Delisle, D.M.; Dress, K.R.; Flahive, E.J.; Hu, Q.; Kuehler, J.E.; Kuki, A.; Liu, W.; McClellan, G.A.; Peng, Q.; Plewe, M.B.; Richardson, P.F.; Smith, G.L.; Solowiej, J.; Tran, K.T.; Wang, H.; Yu, X.; Zhang, J.; Zhu, H. 2011: Design and synthesis of novel N-hydroxy-dihydronaphthyridinones as potent and orally bioavailable HIV-1 integrase inhibitors. Journal of Medicinal Chemistry 54(9): 3393-3417
Adrian Meredith, J.; Wallberg, H.; Vrang, L.; Oscarson, S.; Parkes, K.; Hallberg, A.; Samuelsson, B. 2010: Design and synthesis of novel P2 substituents in diol-based HIV protease inhibitors. European Journal of Medicinal Chemistry 45(1): 160-170
Chen, T.; Jiang, B.; Guo, L. 2010: Design and synthesis of novel PPARgamma agonists. Sichuan da Xue Xue Bao. Yi Xue Ban 41(4): 700-702
Liu, L.Jin.; Hong, J.Hee. 2010: Design and synthesis of novel SATE derivatives of acyclic isocytosine and 9-deazaadenine C-nucleosides. Nucleosides Nucleotides and Nucleic Acids 29(3): 257-266
Isshiki, Y.; Kohchi, Y.; Iikura, H.; Matsubara, Y.; Asoh, K.; Murata, T.; Kohchi, M.; Mizuguchi, E.; Tsujii, S.; Hattori, K.; Miura, T.; Yoshimura, Y.; Aida, S.; Miwa, M.; Saitoh, R.; Murao, N.; Okabe, H.; Belunis, C.; Janson, C.; Lukacs, C.; Schück, V.; Shimma, N. 2011: Design and synthesis of novel allosteric MEK inhibitor CH4987655 as an orally available anticancer agent. Bioorganic and Medicinal Chemistry Letters 21(6): 1795-1801
Ashton, K.S.; St Jean, D.J.; Poon, S.F.; Lee, M.R.; Allen, J.G.; Zhang, S.; Lofgren, J.A.; Zhang, X.; Fotsch, C.; Hungate, R. 2011: Design and synthesis of novel amide AKT1 inhibitors with selectivity over CDK2. Bioorganic and Medicinal Chemistry Letters 21(18): 5191-5196
Tashima, T.; Murata, H.; Kodama, H. 2014: Design and synthesis of novel and highly-active pan-histone deacetylase (pan-HDAC) inhibitors. Bioorganic and Medicinal Chemistry 22(14): 3720-3731
Mallesham, G.; Balaiah, S.; Ananth Reddy, M.; Sridhar, B.; Singh, P.; Srivastava, R.; Bhanuprakash, K.; Jayathirtha Rao, V. 2014: Design and synthesis of novel anthracene derivatives as n-type emitters for electroluminescent devices: a combined experimental and DFT study. Photochemical and Photobiological Sciences: Official Journal of the European Photochemistry Association and the European Society for Photobiology 13(2): 342-357
Shams, H.Z.; Mohareb, R.M.; Helal, M.H.; Mahmoud, A.E.-S. 2011: Design and synthesis of novel antimicrobial acyclic and heterocyclic dyes and their precursors for dyeing and/or textile finishing based on 2-N-acylamino-4,5,6,7-tetrahydro-benzo[b]thiophene systems. Molecules 16(8): 6271-6305
Tiruveedhula, V.V.N.P.B.; Witzigmann, C.M.; Verma, R.; Kabir, M.S.; Rott, M.; Schwan, W.R.; Medina-Bielski, S.; Lane, M.; Close, W.; Polanowski, R.L.; Sherman, D.; Monte, A.; Deschamps, J.R.; Cook, J.M. 2013: Design and synthesis of novel antimicrobials with activity against Gram-positive bacteria and mycobacterial species, including M. tuberculosis. Bioorganic and Medicinal Chemistry 21(24): 7830-7840
Seo, H.J.; Park, E.-J.; Kim, M.J.; Kang, S.Y.; Lee, S.H.; Kim, H.J.; Lee, K.N.; Jung, M.E.; Lee, M.; Kim, M.-S.; Son, E.-J.; Park, W.-K.; Kim, J.; Lee, J. 2011: Design and synthesis of novel arylpiperazine derivatives containing the imidazole core targeting 5-HT(2A) receptor and 5-HT transporter. Journal of Medicinal Chemistry 54(18): 6305-6318
Bourguet, C.B.; Boulay, P.-L.; Claing, A.; Lubell, W.D. 2014: Design and synthesis of novel azapeptide activators of apoptosis mediated by caspase-9 in cancer cells. Bioorganic and Medicinal Chemistry Letters 24(15): 3361-3365
Zhang, H.-Y.; Wang, B.; Sheng, L.; Li, D.; Zhang, D.-F.; Lin, Z.-Y.; Lu, Y.; Li, Y.; Huang, H.-H. 2014: Design and synthesis of novel benzimidazole derivatives as anti-tuberculosis agents. Yao Xue Xue Bao 49(5): 644-651
Luo, Y.; Yao, J.-P.; Yang, L.; Feng, C.-L.; Tang, W.; Wang, G.-F.; Zuo, J.-P.; Lu, W. 2010: Design and synthesis of novel benzimidazole derivatives as inhibitors of hepatitis B virus. Bioorganic and Medicinal Chemistry 18(14): 5048-5055
Hamaguchi, W.; Masuda, N.; Isomura, M.; Miyamoto, S.; Kikuchi, S.; Amano, Y.; Honbou, K.; Mihara, T.; Watanabe, T. 2013: Design and synthesis of novel benzimidazole derivatives as phosphodiesterase 10A inhibitors with reduced CYP1A2 inhibition. Bioorganic and Medicinal Chemistry 21(24): 7612-7623
Chen, Q.; Tian, W.; Han, G.; Qi, J.; Zheng, C.; Zhou, Y.; Ding, L.; Zhao, J.; Zhu, J.; Lv, J.; Sheng, C. 2013: Design and synthesis of novel benzoheterocyclic derivatives as human acrosin inhibitors by scaffold hopping. European Journal of Medicinal Chemistry 59: 176-182
Pingali, H.; Jain, M.; Shah, S.; Zaware, P.; Makadia, P.; Pola, S.; Thube, B.; Patel, D.; Patil, P.; Priyadarshini, P.; Suthar, D.; Shah, M.; Giri, S.; Patel, P. 2010: Design and synthesis of novel bis-oximinoalkanoic acids as potent PPAR alpha agonists. Bioorganic and Medicinal Chemistry Letters 20(3): 1156-1161
Sarkis, M.; Tran, D.N.; Kolb, S.ép.; Miteva, M.A.; Villoutreix, B.O.; Garbay, C.; Braud, E. 2012: Design and synthesis of novel bis-thiazolone derivatives as micromolar CDC25 phosphatase inhibitors: effect of dimerisation on phosphatase inhibition. Bioorganic and Medicinal Chemistry Letters 22(24): 7345-7350
Arns, S.; Gibe, R.; Moreau, A.; Monzur Morshed, M.; Young, R.N. 2012: Design and synthesis of novel bone-targeting dual-action pro-drugs for the treatment and reversal of osteoporosis. Bioorganic and Medicinal Chemistry 20(6): 2131-2140
Liu, Y-Qian.; Dai, W.; Yang, L.; Li, H-Yu. 2011: Design and synthesis of novel camptothecin/5-fluorouracil conjugates as cytotoxic agents. Natural Product Research 25(19): 1817-1826
Oh, C.Hyun.; Kim, E.; Hong, J.Hee. 2011: Design and synthesis of novel carbocyclic versions of 2'-spirocyclopropyl ribonucleosides as potent anti-HCV agents. Nucleosides Nucleotides and Nucleic Acids 30(6): 423-439
Li, Y.; Zhou, Y.; Ma, Y.; Li, X. 2011: Design and synthesis of novel cell wall inhibitors of Mycobacterium tuberculosis GlmM and GlmU. Carbohydrate Research 346(13): 1714-1720
Yang, K.; Wang, Q.; Su, L.; Fang, H.; Wang, X.; Gong, J.; Wang, B.; Xu, W. 2009: Design and synthesis of novel chloramphenicol amine derivatives as potent aminopeptidase N (APN/CD13) inhibitors. Bioorganic and Medicinal Chemistry 17(11): 3810-3817
Venkateswararao, E.; Sharma, V.K.; Lee, K.-C.; Roh, E.; Kim, Y.; Jung, S.-H. 2013: Design and synthesis of novel chromenone derivatives as interleukin-5 inhibitors. Bioorganic and Medicinal Chemistry 21(9): 2543-2550
El-Gamel, N.E.A.; Farghaly, T.A. 2013: Design and synthesis of novel complexes containing N-phenyl-1H-pyrazole moiety: Ni complex as potential antifungal and antiproliferative compound. Spectrochimica Acta. Part a Molecular and Biomolecular Spectroscopy 115: 469-475
Fukai, R.; Zheng, X.; Motoshima, K.; Tai, A.; Yazama, F.; Kakuta, H. 2011: Design and synthesis of novel cyclooxygenase-1 inhibitors as analgesics: 5-amino-2-ethoxy-N-(substituted-phenyl)benzamides. Chemmedchem 6(3): 550-560
Li, H.-Q.; Luo, Y.; Lv, P.-C.; Shi, L.; Liu, C.-H.; Zhu, H.-L. 2010: Design and synthesis of novel deoxybenzoin derivatives as FabH inhibitors and anti-inflammatory agents. Bioorganic and Medicinal Chemistry Letters 20(6): 2025-2028
Schinke, C.; Goel, S.; Bhagat, T.D.; Zhou, L.; Mo, Y.; Gallagher, R.; Kabalka, G.W.; Platanias, L.C.; Verma, A.; Das, B. 2010: Design and synthesis of novel derivatives of all-trans retinoic acid demonstrate the combined importance of acid moiety and conjugated double bonds in its binding to PML-RAR-alpha oncogene in acute promyelocytic leukemia. Leukemia and Lymphoma 51(6): 1108-1114
Dehnhardt, C.M.; Venkatesan, A.M.; Chen, Z.; Ayral-Kaloustian, S.; Dos Santos, O.; Delos Santos, E.; Curran, K.; Follettie, M.T.; Diesl, V.; Lucas, J.; Geng, Y.; Dejoy, S.Q.; Petersen, R.; Chaudhary, I.; Brooijmans, N.; Mansour, T.S.; Arndt, K.; Chen, L. 2010: Design and synthesis of novel diaminoquinazolines with in vivo efficacy for beta-catenin/T-cell transcriptional factor 4 pathway inhibition. Journal of Medicinal Chemistry 53(2): 897-910
Nikalje, A.P.G.; Ghodke, M.; Girbane, A. 2012: Design and synthesis of novel diphenyl oxalamide and diphenyl acetamide derivatives as anticonvulsants. Archiv der Pharmazie 345(1): 57-64
Li, C.; Ma, C.; Zhang, J.; Qian, N.; Ding, J.; Qiao, R.; Zhao, Y. 2014: Design and synthesis of novel distamycin-modified nucleoside analogues as HIV-1 reverse transcriptase inhibitors. Antiviral Research 102: 54-60
Chen, J.-B.; Liu, E.M.; Chern, T.-R.; Yang, C.-W.; Lin, C.-I.; Huang, N.-K.; Lin, Y.-L.; Chern, Y.; Lin, J.-H.; Fang, J.-M. 2011: Design and synthesis of novel dual-action compounds targeting the adenosine A(2A) receptor and adenosine transporter for neuroprotection. Chemmedchem 6(8): 1390-1400
Lee, M.; Brockway, O.; Dandavati, A.; Tzou, S.; Sjoholm, R.; Nickols, A.; Babu, B.; Chavda, S.; Satam, V.; Hartley, R.M.; Westbrook, C.; Mooberry, S.L.; Fraley, G.; Lee, M. 2011: Design and synthesis of novel enhanced water soluble hydroxyethyl analogs of combretastatin A-4. Bioorganic and Medicinal Chemistry Letters 21(7): 2087-2091
Sawant, R.R.; Torchilin, V.P. 2011: Design and synthesis of novel functional lipid-based bioconjugates for drug delivery and other applications. Methods in Molecular Biology 751: 357-378
Canzoneri, J.C.; Chen, P.C.; Oyelere, A.K. 2009: Design and synthesis of novel histone deacetylase inhibitor derived from nuclear localization signal peptide. Bioorganic and Medicinal Chemistry Letters 19(23): 6588-6590
Ishikawa, T.; Seto, M.; Banno, H.; Kawakita, Y.; Oorui, M.; Taniguchi, T.; Ohta, Y.; Tamura, T.; Nakayama, A.; Miki, H.; Kamiguchi, H.; Tanaka, T.; Habuka, N.; Sogabe, S.; Yano, J.; Aertgeerts, K.; Kamiyama, K. 2011: Design and synthesis of novel human epidermal growth factor receptor 2 (HER2)/epidermal growth factor receptor (EGFR) dual inhibitors bearing a pyrrolo[3,2-d]pyrimidine scaffold. Journal of Medicinal Chemistry 54(23): 8030-8050
Ghosh, S.; Pignot-Paintrand, I.; Dumy, P.; Defrancq, E. 2009: Design and synthesis of novel hybrid metal complex-DNA conjugates: key building blocks for multimetallic linear DNA nanoarrays. Organic and Biomolecular Chemistry 7(13): 2729-2737
Thanigaimalai, P.; Lee, K.-C.; Sharma, V.K.; Yun, J.-H.; Kim, Y.; Jung, S.-H. 2010: Design and synthesis of novel hydroxyalkylaminomethylchromones for their IL-5 inhibitory activity. Bioorganic and Medicinal Chemistry 18(13): 4625-4629