铜绿假单胞菌
化学
抗菌活性
四环素
广谱
体外
体内
微生物学
抗菌剂
抗生素
喹诺酮类
组合化学
立体化学
细菌
生物化学
生物
生物技术
遗传学
作者
Yonghong Deng,Cuixiang Sun,Diana K. Hunt,Corey Fyfe,Chi-Li Chen,Trudy H. Grossman,Joyce A. Sutcliffe,Xiao-Yi Xiao
标识
DOI:10.1021/acs.jmedchem.6b01903
摘要
Utilizing a total synthesis approach, the first 8-heterocyclyltetracyclines were designed, synthesized, and evaluated against panels of tetracycline- and multidrug-resistant Gram-positive and Gram-negative pathogens. Several compounds with balanced, highly potent in vitro activity against a broad range of bacterial isolates were identified through structure-activity relationships (SAR) studies. One compound demonstrated the best antibacterial activity against Pseudomonas aeruginosa both in vitro and in vivo for tetracyclines reported to date.
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