Structural modifications and biological evaluation of 3-isoxazolylvinylcephalosporins
- Authors
- Pae, AN; Lee, JE; Kim, BH; Cha, JH; Kim, HY; Cho, YS; Choi, KI; Koh, HY; Lee, E; Kim, 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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