Substituted pyrazoles as novel sEH antagonist: Investigation of key binding interactions within the catalytic domain
摘要:
A novel series of pyrazole sEH inhibitors is reported. Lead optimization efforts to replace the aniline core are also described. In particular, 2-pyridine, 3-pyridine and pyridazine analogs are potent sEH inhibitors with favorable CYP3A4 inhibitory and microsomal stability profiles. (C) 2010 Elsevier Ltd. All rights reserved.
Substituted pyrazole compounds useful as soluble epoxide hyrolase inhibitors
申请人:Fleck Roman Wolfgang
公开号:US20090227588A1
公开(公告)日:2009-09-10
Disclosed are compounds active against soluble epoxide hydrolase (sEH), compositions thereof and methods of using and making same.
本发明涉及对可溶性环氧水解酶(sEH)活性的化合物,其组成物和使用和制备它们的方法。
WO2007/67836
申请人:——
公开号:——
公开(公告)日:——
SUBSTITUTED PYRAZOLE COMPOUNDS USEFUL AS SOLUBLE EPOXIDE HYDROLASE INHIBITORS
申请人:Boehringer Ingelheim International GmbH
公开号:EP1960367A2
公开(公告)日:2008-08-27
[EN] SUBSTITUTED PYRAZOLE COMPOUNDS USEFUL AS SOLUBLE EPOXIDE HYDROLASE INHIBITORS<br/>[FR] COMPOSES DE PYRAZOLE SUBSTITUES UTILES EN TANT QU'INHIBITEURS D'EPOXYDE HYDROLASE SOLUBLE
申请人:BOEHRINGER INGELHEIM INT
公开号:WO2007067836A2
公开(公告)日:2007-06-14
[EN] Disclosed are compounds active against soluble epoxide hydrolase (sEH), compositions thereof and methods of using and making same. [FR] La présente invention concerne des composés actifs contre l'époxyde hydrolase soluble (sEH), des compositions de ceux-ci et des procédés d'utilisation de ceux-ci.
Substituted pyrazoles as novel sEH antagonist: Investigation of key binding interactions within the catalytic domain
作者:Ho Yin Lo、Chuk C. Man、Roman W. Fleck、Neil A. Farrow、Richard H. Ingraham、Alison Kukulka、John R. Proudfoot、Raj Betageri、Tom Kirrane、Usha Patel、Rajiv Sharma、Mary Ann Hoermann、Alisa Kabcenell、Stéphane De Lombaert
DOI:10.1016/j.bmcl.2010.09.095
日期:2010.11
A novel series of pyrazole sEH inhibitors is reported. Lead optimization efforts to replace the aniline core are also described. In particular, 2-pyridine, 3-pyridine and pyridazine analogs are potent sEH inhibitors with favorable CYP3A4 inhibitory and microsomal stability profiles. (C) 2010 Elsevier Ltd. All rights reserved.