Optimization of a pyrazole hit from FBDD into a novel series of indazoles as ketohexokinase inhibitors
摘要:
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. (C) 2011 Elsevier Ltd. All rights reserved.
INDAZOLE COMPOUNDS USEFUL AS KETOHEXOKINASE INHIBITORS
申请人:ZHANG Xuqing
公开号:US20110263559A1
公开(公告)日:2011-10-27
The present invention is directed to substituted indazole compounds, pharmaceutical compositions of these compounds and methods of use thereof. The compounds of the present invention are ketohexokinase (KHK) inhibitors, useful for treating or ameliorating a KHK mediated metabolic disorders and/or diseases such as obesity, Type II diabetes mellitus and Metabolic Syndrome X.
[EN] INDAZOLE COMPOUNDS USEFUL AS KETOHEXOKINASE INHIBITORS<br/>[FR] INDAZOLES EN TANT QU'INHIBITEURS DE CÉTOHEXOKINASE
申请人:JANSSEN PHARMACEUTICA NV
公开号:WO2011133750A1
公开(公告)日:2011-10-27
The present invention is directed to substituted indazole compounds, pharmaceutical compositions of these compounds and methods of use thereof. The compounds of the present invention are ketohexokinase (KHK) inhibitors, useful for treating or ameliorating a KHK mediated metabolic disorders and / or diseases such as obesity, Type II diabetes mellitus and Metabolic Syndrome X.
Optimization of a pyrazole hit from FBDD into a novel series of indazoles as ketohexokinase inhibitors
作者:Xuqing Zhang、Fengbing Song、Gee-Hong Kuo、Amy Xiang、Alan C. Gibbs、Marta C. Abad、Weimei Sun、Lawrence C. Kuo、Zhihua Sui
DOI:10.1016/j.bmcl.2011.06.067
日期:2011.8
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. (C) 2011 Elsevier Ltd. All rights reserved.