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诺卡硫霉素类似物:新型水溶性酰胺的合成与抗菌活性

Nocathiacin analogs: Synthesis and antibacterial activity of novel water-soluble amides.

作者信息

Xu Libo, Farthing Amy K, Dropinski James F, Meinke Peter T, McCallum Christine, Leavitt Penny S, Hickey Emily J, Colwell Lawrence, Barrett John, Liu Kun

机构信息

Merck Research Laboratories, PO Box 2000, Rahway, NJ 07065, USA.

出版信息

Bioorg Med Chem Lett. 2009 Jul 1;19(13):3531-5. doi: 10.1016/j.bmcl.2009.04.144. Epub 2009 May 5.

Abstract

Novel water-soluble amide analogs were synthesized from nocathiacin I (1) through the formation of the carboxylic acid intermediate followed by coupling to primary or secondary amines. Several compounds with potent antibacterial activity and adequate water solubility were identified. Of these, compound 19 was selected for more extensive evaluation because of its excellent in vitro antibacterial activity and in vivo efficacy, as well as clean off-target screening.

摘要

新型水溶性酰胺类似物由诺卡硫霉素I(1)合成,通过形成羧酸中间体,然后与伯胺或仲胺偶联。鉴定出了几种具有强效抗菌活性和足够水溶性的化合物。其中,化合物19因其出色的体外抗菌活性、体内疗效以及良好的脱靶筛选结果而被选作更广泛的评估对象。

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