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发现具有体内活性的哌嗪酸肽脱甲酰基酶抑制剂,可用于治疗呼吸道和皮肤感染。

Discovery of piperazic acid peptide deformylase inhibitors with in vivo activity for respiratory tract and skin infections.

机构信息

GlaxoSmithKline, 1250 S. Collegeville Rd., Collegeville, PA 19426, USA.

GlaxoSmithKline, 1250 S. Collegeville Rd., Collegeville, PA 19426, USA.

出版信息

Bioorg Med Chem Lett. 2019 Aug 15;29(16):2410-2414. doi: 10.1016/j.bmcl.2019.05.028. Epub 2019 May 16.

Abstract

The discovery of a novel series of peptide deformylase inhibitors incorporating a piperazic acid amino acid found in nature is described. These compounds demonstrated potent in vitro enzymatic potency and antimicrobial activity. Crystal structure analysis revealed the piperazic acid optimized a key contact with the PDF protein that accounted for the increased enzymatic potency of these compounds. We describe lead optimization of the P3' region of the series that resulted in a compound with good potency against three target organisms. One molecule showed in vivo efficacy in a rat respiratory infection model but ultimately did not meet candidate progression criteria.

摘要

本文描述了一种新型肽脱甲酰酶抑制剂的发现,其中包含了在自然界中发现的哌嗪酸氨基酸。这些化合物表现出很强的体外酶活性和抗菌活性。晶体结构分析表明,哌嗪酸优化了与 PDF 蛋白的关键接触,这解释了这些化合物酶活性的提高。我们描述了该系列化合物 P3' 区域的先导优化,得到了一个对三种靶标生物具有良好活性的化合物。一种化合物在大鼠呼吸道感染模型中表现出体内疗效,但最终未达到候选药物推进标准。

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