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从 FBDD 中优化吡唑类命中物得到新型吲哚类酮己糖激酶抑制剂。

Optimization of a pyrazole hit from FBDD into a novel series of indazoles as ketohexokinase inhibitors.

机构信息

Johnson & Johnson Pharmaceutical Research and Development, Welsh & McKean Roads, PO Box 776, Spring House, PA 19477, United States.

出版信息

Bioorg Med Chem Lett. 2011 Aug 15;21(16):4762-7. doi: 10.1016/j.bmcl.2011.06.067. Epub 2011 Jun 29.

Abstract

A series of indazoles have been discovered as KHK inhibitors from a pyrazole hit identified through fragment-based drug discovery (FBDD). The optimization process guided by both X-ray crystallography and solution activity resulted in lead-like compounds with good pharmaceutical properties.

摘要

一系列吲唑类化合物已被发现是通过基于片段的药物发现(FBDD)鉴定的吡唑命中的 KHK 抑制剂。X 射线晶体学和溶液活性指导的优化过程产生了具有良好药物性质的类先导化合物。

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