Structural modifications and biological evaluation of 3-isoxazolylvinylcephalosporins

Authors
Pae, ANLee, JEKim, BHCha, JHKim, HYCho, YSChoi, KIKoh, HYLee, EKim, JH
Issue Date
2000-07-28
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Citation
TETRAHEDRON, v.56, no.31, pp.5657 - 5665
Abstract
Structural modifications and biological evaluations of 3-isoxazolylvinylcephalosporins (I) were performed. The replacement of a hydrogen atom at the 7-aminothiazole group by a chlorine resulted in an improvement: of the activity against resistant Gram-positive bacterial strains including the methicillin-resistant Staphylococcus aureus (MRSA) and the ciprofloxacin-resistant Staphylococcus aureus (CRSA). The introduction of other heterocycles such as an isothiazole or a thiadiazole in place of the isoxazole moiety gave slightly decreased in vitro activities. (C) 2000 Elsevier Science Ltd. All rights reserved.
Keywords
CATECHOL MOIETY; C-7 POSITION; CEPHALOSPORINS; DERIVATIVES; CATECHOL MOIETY; C-7 POSITION; CEPHALOSPORINS; DERIVATIVES; antibacterials; cephalosporins; isoxazoles; thiazoles
ISSN
0040-4020
URI
https://pubs.kist.re.kr/handle/201004/141223
DOI
10.1016/S0040-4020(00)00415-4
Appears in Collections:
KIST Article > 2000
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