Discovery of piperidine-aryl urea-based stearoyl-CoA desaturase 1 inhibitors
摘要:
A series of structurally novel stearoyl-CoA desaturase1 (SCD1) inhibitors has been identified via molecular scaffold manipulation. Preliminary structure-activity relationship (SAR) studies led to the discovery of potent, and orally bioavailable piperidine-aryl urea-based SCD1 inhibitors. 4-(2-Chlorophenoxy)-N-[3-(methyl carbamoyl)phenyl]piperidine-1-carboxamide 4c exhibited robust in vivo activity with dose-dependent desaturation index lowering effects. (c) 2008 Elsevier Ltd. All rights reserved.
SOLUBLE EPOXIDE HYDROLASE INHIBITORS AND METHODS OF USING SAME
申请人:Boehringer Ingelheim International GmbH
公开号:EP1996545A1
公开(公告)日:2008-12-03
COMPOUNDS AND USES THEREOF
申请人:Yumanity Therapeutics, Inc.
公开号:EP3914593A1
公开(公告)日:2021-12-01
[EN] SOLUBLE EPOXIDE HYDROLASE INHIBITORS AND METHODS OF USING SAME<br/>[FR] INHIBITEURS D'EPOXYDE HYDROLASE SOLUBLES ET PROCEDES D'UTILISATION CORRESPONDANT
申请人:BOEHRINGER INGELHEIM INT
公开号:WO2007106705A1
公开(公告)日:2007-09-20
[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 dérivées et des procédés d'utilisation et de fabrication correspondant.