Semisynthetic .Beta.-lactam antibiotics. Ii Synthesis and antibacterial activity of 7.Beta.- (2- (acylamino) -2- (2-aminothiazol-4-yl) acetamido) cephalosporins

Arimoto, M.; Ejima, A.; Watanabe, T.; Tagawa, H.; Furukawa, M.

The Journal of Antibiotics 39(9): 1236-1242

1986


DOI: 10.7164/antibiotics.39.1236
Accession: 068516206

Download citation:  
Text
  |  
BibTeX
  |  
RIS

Article/Abstract emailed within 0-6 h
Payments are secure & encrypted
Powered by Stripe
Powered by PayPal

Abstract
Cephalosporin derivatives (I) substituted with a neutral, acidic or basic amino acid group as the terminal group attached to the 2-amino-2-(2-aminothiazol-4-yl)acetamido side chain at the C-7 position were synthesized, and the effect of each group on antibacterial activity was examined. The derivatives bearing an amidino or guanidino group showed broad spectra of antibacterial activity similar to those of cefotaxime, but they were relatively sensitive to beta-lactamases.