Discovery of piperidine carboxamide TRPV1 antagonists
摘要:
A series of piperidine carboxamides were developed as potent antagonists of the transient receptor potential vanilloid-1 (TRPV1), an emerging target for the treatment of pain. A focused library of polar head groups led to the identification of a benzoxazinone amide that afforded good potency in cell-based assays. Synthesis and a QSAR model will be presented. (C) 2008 Elsevier Ltd. All rights reserved.
[EN] 4-PIPERIDINECARBOXAMIDE MODULATORS OF VANILLOID VR1 RECEPTOR<br/>[FR] MODULATEURS DE 4-PIPERIDINECARBOXAMIDE DU RECEPTEUR VANILLOIDE VR1
申请人:JANSSEN PHARMACEUTICA NV
公开号:WO2006058338A2
公开(公告)日:2006-06-01
[EN] This invention is directed to vanilloid receptor VR1 ligands. More particularly, this invention relates to hetero isonipecotic amides that are potent modulators of VR1 which are useful for the treatment and prevention of disease conditions in mammals. [FR] Cette invention concerne des ligands du récepteur vanilloïde VR1. Plus particulièrement, l'invention concerne des amides isonipecotiques qui sont des modulateurs puissants convenant pour le traitement et la prévention de divers états pathologiques chez les mammifères.
4-Piperidinecarboxamide modulators of vanilloid VR1 receptor
申请人:Calvo R. Raul
公开号:US20060116368A1
公开(公告)日:2006-06-01
This invention is directed to vanilloid receptor VR1 ligands. More particularly, this invention relates to hetero isonipecotic amides that are potent modulators of VR1 which are useful for the treatment and prevention of disease conditions in mammals.
Discovery of piperidine carboxamide TRPV1 antagonists
作者:Wing S. Cheung、Raul R. Calvo、Brett A. Tounge、Sui-Po Zhang、Dennis R. Stone、Michael R. Brandt、Tasha Hutchinson、Christopher M. Flores、Mark R. Player
DOI:10.1016/j.bmcl.2008.07.035
日期:2008.8
A series of piperidine carboxamides were developed as potent antagonists of the transient receptor potential vanilloid-1 (TRPV1), an emerging target for the treatment of pain. A focused library of polar head groups led to the identification of a benzoxazinone amide that afforded good potency in cell-based assays. Synthesis and a QSAR model will be presented. (C) 2008 Elsevier Ltd. All rights reserved.