头孢菌素
儿茶酚
铜绿假单胞菌
铁载体
微生物学
化学
假单胞菌
细菌
生物
抗生素
生物化学
遗传学
基因
作者
Moon-Soo Chang,Heeyuen Koh,Younghak Cho,Kyung II Choi
标识
DOI:10.2174/138161280302221006120722
摘要
Abstract: Since the catechol type cephalosporins having a potent activity against P. aeruginosa strain were introduced, many kinds of derivatives have been developed. These cephalosporins adopted various substituents as siderophores such as catechol or pyridone type derivatives at C-7 or C-3 position to facilitate their penetration through the bacterial cell membrane. In this review, the structural specifications of the recently developed cephalosporins and their biological activity against P. aeruginosa bacterial strain would be overviewed.
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