Chen J X, Guo H Y
Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences, Beijing.
Yao Xue Xue Bao. 1991;26(10):733-40.
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.
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。