NOVEL CEPHALOSPORIN DERIVATIVES POSSESSING A BICYCLIC HETERO-CYCLE ATTHE 3-POSITION - PART II - SYNTHESIS AND ANTIBACTERIAL ACTIVITY OF OLO[4,5-C]PYRIDINIUM-2-YL)-THIOMETHYLCEPHALOSPORIN DERIVATIVES AND RELATED-COMPOUNDS

Citation
M. Tsushima et al., NOVEL CEPHALOSPORIN DERIVATIVES POSSESSING A BICYCLIC HETERO-CYCLE ATTHE 3-POSITION - PART II - SYNTHESIS AND ANTIBACTERIAL ACTIVITY OF OLO[4,5-C]PYRIDINIUM-2-YL)-THIOMETHYLCEPHALOSPORIN DERIVATIVES AND RELATED-COMPOUNDS, Bioorganic & medicinal chemistry, 6(9), 1998, pp. 1641-1653
Citations number
7
Categorie Soggetti
Biology,"Chemistry Medicinal","Chemistry Inorganic & Nuclear
ISSN journal
09680896
Volume
6
Issue
9
Year of publication
1998
Pages
1641 - 1653
Database
ISI
SICI code
0968-0896(1998)6:9<1641:NCDPAB>2.0.ZU;2-F
Abstract
A series of cephalosporin derivatives with a thiazolopyridinium group at the 3-position was synthesized and evaluated for antibacterial acti vity. Some of these cephalosporin derivatives having a (5-alkylthiazol o[4,5-c]pyridinium-2-yl)thiomethyl group at the 3-position showed stro ng activity against Gram-positive and Gram-negative bacteria, includin g Pseudomonas aeruginosa. Among them, 5a showed a good antibacterial s pectrum in vitro, and also showed a similar or slightly superior activ ity to that of ceftazidime in vivo against P. aeruginosa. (C) 1998 Els evier Science Ltd. All rights reserved.