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[吡啶酮羧酸类抗菌剂的研究。X. 1,7-二取代-6-氟-1,4-二氢-4-氧代喹啉-3-羧酸的合成及其构效关系]

[Studies on pyridonecarboxylic acids as antibacterial agents. X. Synthesis and structure-activity relationships of 1, 7-disubstituted-6-fluoro-1,4-dihydro-4-oxo-quinoline-3-carboxylic acids].

作者信息

Chen J X, Guo H Y

机构信息

Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences, Beijing.

出版信息

Yao Xue Xue Bao. 1991;26(10):733-40.

PMID:1823714
Abstract

A series of pyridonecarboxylic acids were prepared. These compounds have different groups including substituted benzenes, furans and isoxazles at the 1-position, or different substituted amino groups at the 7-position. The in vitro antibacterial potencies of these compounds against E. coli. and S. aureus were tested, and structure-activity relationships were discussed.

摘要

制备了一系列吡啶酮羧酸。这些化合物在1位具有不同的基团,包括取代苯、呋喃和异恶唑,或者在7位具有不同的取代氨基。测试了这些化合物对大肠杆菌和金黄色葡萄球菌的体外抗菌效力,并讨论了构效关系。

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