Chemical modification of erythromycins. III, In vitro and In vivo antibacterial activities of new semisynthetic 6-O-methylerythromycins A, TE-031 (clarithromycin) and TE-032
Morimoto, S.; Nagate, T.; Sugita, S.; Ono, T.; Numata, K.; Miyachi, J.; Misawa, Y.; Yamada, K.; Omura, S.
Journal of Antibiotics (Tokyo 1968) 43(3): 295-305
1990
ISSN/ISBN: 0021-8820 Accession: 074409672
PDF emailed within 1 workday: $29.90
Related References
Morimoto, S.; Nagate, T.; Sugita, K.; Ono, T.; Numata, K.; Miyachi, J.; Misawa, Y.; Yamada, K.; Omura, S. 1990: Chemical modification of erythromycins. III. in vitro and in vivo antibacterial activities of new semisynthetic 6-O-methylerythromycins A, TE-031 (clarithromycin) and TE-032 Journal of Antibiotics 43(3): 295-305Morimoto, S.; Takahashi, Y.; Watanabe, Y.; Omura, S. 1984: Chemical modification of erythromycins. I. Synthesis and antibacterial activity of 6-O-methylerythromycins a Journal of Antibiotics 37(2): 187-189
Morimoto, S.; Takahashi, Y.; Watanabe, Y.; Omura, S. 1984: Chemical modification of erythromycins. I: Synthesis and antibacterial activity of 6-O-methylerythromycins A Journal of Antibiotics (Tokyo 1968) 37(2): 187-189
Morimoto, S.; Misawa, Y.; Asaka, T.; Kondoh, H.; Watanabe, Y. 1990: Chemical modification of erythromycins. VI. Structure and antibacterial activity of acid degradation products of 6-O-methylerythromycins a Journal of Antibiotics 43(5): 570-573
Morimoto, S.; Misawa, Y.; Asaka, T.; Kondoh, H.; Watanabe, Y. 1990: Chemical modification of erythromycins. VI, Structure and antibacterial activity of acid degradation products of 6-O-methylerythromycins A Journal of Antibiotics (Tokyo 1968) 43(5): 570-573
Watanabe, Y.; Adachi, T.; Asaka, T.; Kashimura, M.; Morimoto, S. 1990: Chemical modification of erythromycins. VIII, A new effective route to clarithromycin (6-O-methylerythromycin A) eng Heterocycles (Sendai) 31(12): 2121-2124
Watanabe, Y.; Adachi, T.; Asaka, T.; Kashimura, M.; Morimoto, S. 1990: Chemical modification of erythromycins viii. a new effective route to clarithromycin 6 o methylerythromycin a Heterocycles 31(12): 2121-2124
Ono, T.; Numata, K.; Nagate, T.; Mitsuhashi, S.; Inoue, M. 1996: In vitro and in vivo antibacterial activities of clarithromycin Chemotherapy 42(3): 159-169
Saino, Y.; Hattori, Y.; Koshi, T.; Kobayashi, F.; Oda, T.; Mitsuhashi, S. 1984: In vitro and in vivo antibacterial activities of K-4619, a new semisynthetic aminoglycoside Antimicrobial Agents and ChemoTherapy 26(2): 187-191
Inouye, S.; Goi, H.; Watanabe, T.; Hara, T.; Miyauchi, K.; Yoshida, T.; Kazuno, Y.; Kadosawa, H.; Hirano, F.; Kawaharajo, K. 1984: In vitro and in vivo antibacterial activities of MT-141, a new semisynthetic cephamycin, compared with those of five cephalosporins Antimicrobial Agents and ChemoTherapy 26(5): 722-729
Inouye, S.; Goi, H.; Watanabe, T.; Hara, T.; Miyauchi, K.; Yoshida, T.; Kazuno, Y.; Kadosawa, H.; Hirano, F.; Kawaharajo, K.; Orikasa, Y.; Nishino, T. 1985: In Vitro and In Vivo Antibacterial Activities of MT-141, a New Semisynthetic Cephamycin, Compared with Those of Five Cephalosporins Antimicrobial Agents and ChemoTherapy 27(5): 882-882
Testa, R.T.; Petersen, P.J.; Jacobus, N.V.; Sum, P.E.; Lee, V.J.; Tally, F.P. 1993: In vitro and in vivo antibacterial activities of the glycylcyclines, a new class of semisynthetic tetracyclines Antimicrobial Agents and ChemoTherapy 37(11): 2270-2277
Watanabe, Y.; Adachi, T.; Asaka, T.; Kashimura, M.; Matsunaga, T.; Morimoto, S. 1993: Chemical modification of erythromycins. XII: A facile synthesis of clarithromycin (6-O-methylerythromycin A) via 2'-silylethers of erythromycin a derivatives Journal of Antibiotics (Tokyo 1968) 46(7): 1163-1167
Morimoto, S.; Adachi, T.; Watanabe, Y.; Omura, S. 1990: Chemical modification of erythromycins vii. molecular rearrangement observed during chemical modification study of the desosamine unit of erythromycins Heterocycles 31(2): 305-320
Watanabe, Y.; Adachi, T.; Asaka, T.; Kashimura, M.; Matsunaga, T.; Morimoto, S. 1993: Chemical modification of erythromycins. Xii. A facile synthesis of clarithromycin(6-O-methylerythromycin A) via 2'-silylethers of erythromycin a derivatives The Journal of Antibiotics 46(7): 1163-1167
Watanabe, Y.; Kashimura, M.; Asaka, T.; Adachi, T.; Morimoto, S. 1993: Chemical modification of erythromycins. XI: Synthesis of clarithromycin (6-O-methylerythromycin A) via erythromycin A quaternary ammonium salt derivative Heterocycles (Sendai) 36(2): 243-247
Watanabe, Y.; Adachi, T.; Asaka, T.; Kashimura, M.; Matsunaga, T.; Morimoto, S. 1993: Chemical modification of erythromycins. XII. a facile synthesis of clarithromycin (6-O-methylerythromycin A) via 2'-silylethers of erythromycin a derivatives Journal of Antibiotics 46(7): 1163-1167
Watanabe, Y.; Morimoto, S.; Adachi, T.; Kashimura, M.; Asaka, T. 1993: Chemical modification of erythromycins. IX. Selective methylation at the C-6 hydroxyl group of erythromycin A oxime derivatives and preparation of clarithromycin Journal of Antibiotics 46(4): 647-660
Watanabe, Y.; Morimoto, S.; Adachi, T.; Kashimura, M.; Asaka, T. 1993: Chemical modification of erythromycins. IX: Selective methylation at the C-6 hydroxyl group of erythromycin A oxime derivatives and preparation of clarithromycin Journal of Antibiotics (Tokyo 1968) 46(4): 647-660
Morimoto, S.; Misawa, Y.; Adachi, T.; Nagate, T.; Watanabe, Y.; Omura, S. 1990: Chemical modification of erythromycins. II. Synthesis and antibacterial activity of O-alkyl derivatives of erythromycin a Journal of Antibiotics 43(3): 286-294