期刊
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
卷 69, 期 -, 页码 622-631出版社
ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.ejmech.2013.07.040
关键词
7-Aminocephalosporanic acid; 1,3-Oxazole; 1,3-Thiazole; Antimicrobial activity; Anti-urease activity; Anti beta-lactamase activity
资金
- Scientific and Technological Research Council of Turkey (TUBITAK) [111T427]
The treatment of 7-ACA with 4-substituted benzensulfonyl chlorides afforded the compounds containing 4-nitro/aminophenyl sulfonylamino moiety in the cephalosporanic acid skeleton (2, 4). The synthesis of the cephalosporanic acid derivatives containing 1,3-thiazole or 5-oxo-1,3-thiazolidine nucleus and sulfonamide function (8a, 8b, 10) was performed starting from 7-ACA by several steps. The reaction of 7ACA with [4-(2-fluoro-4-nitrophenyl)piperazin-1-yl]acetyl chloride afforded the corresponding 7{[4-(2-fluoro-4-nitrophenyl)piperazin-1-yl]acetyl)amino derivative (13). The synthesized compounds were screened for their antimicrobial and antiurease activities. Some of them were found to possess good moderate antimicrobial activity against the test microorganisms. Compound 5d was observed to have moderate anti-urease activity. (C) 2013 Elsevier Masson SAS. All rights reserved.
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