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一种用于开发水溶性氟喹诺酮类药物的前药方法及喹啉-3-羧酸的构效关系。

A prodrug approach toward the development of water soluble fluoroquinolones and structure--activity relationships of quinoline-3-carboxylic acids.

作者信息

Baker William R, Cai Shaopei, Dimitroff Martin, Fang Liming, Huh Kay K, Ryckman David R, Shang Xiao, Shawar Ribhi M, Therrien Joseph H

机构信息

Chiron Corporation, 201 Elliott Avenue West, Seattle, Washington 98119, USA.

出版信息

J Med Chem. 2004 Sep 9;47(19):4693-709. doi: 10.1021/jm0497895.

Abstract

A fluoroquinolone prodrug, PA2808, was prepared and shown to convert to the highly active parent drug PA2789. In vitro and in vivo activation of PA2808 by alkaline phosphatase was demonstrated using disk diffusion and rat lung infection models. The water solubility of PA2808 showed a marked increase compared to PA2789 over a pH range suitable for aerosol drug delivery. A total of 48 analogues based on PA2789 were prepared and screened against a panel of Gram-positive and Gram-negative pathogens. Incorporating a cyclopropane-fused pyrrolidine (amine) at C-7 resulted in some of the most active analogues.

摘要

制备了一种氟喹诺酮前药PA2808,结果表明它可转化为高活性的母体药物PA2789。使用纸片扩散法和大鼠肺部感染模型证明了碱性磷酸酶在体外和体内对PA2808的激活作用。在适合气溶胶给药的pH范围内,PA2808的水溶性与PA2789相比显著增加。基于PA2789总共制备了48种类似物,并针对一组革兰氏阳性和革兰氏阴性病原体进行了筛选。在C-7位引入环丙烷稠合的吡咯烷(胺)得到了一些活性最强的类似物。

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