Heteroaryl β-tetralin ureas as novel antagonists of human TRPV1
摘要:
We report on a series of alpha-substituted-beta-tetralin-derived and related phenethyl-based isoquinolinyl and hydroxynaphthyl ureas as potent antagonists of the human TRPV1 receptor. The synthesis and Structure-activity relationships (SAR) of the series are described. (C) 2007 Elsevier Ltd. All rights reserved.
Heteroaryl β-tetralin ureas as novel antagonists of human TRPV1
摘要:
We report on a series of alpha-substituted-beta-tetralin-derived and related phenethyl-based isoquinolinyl and hydroxynaphthyl ureas as potent antagonists of the human TRPV1 receptor. The synthesis and Structure-activity relationships (SAR) of the series are described. (C) 2007 Elsevier Ltd. All rights reserved.
Heteroaryl β-tetralin ureas as novel antagonists of human TRPV1
作者:Michele C. Jetter、Mark A. Youngman、James J. McNally、Mark E. McDonnell、Sui-Po Zhang、Adrienne E. Dubin、Nadia Nasser、Ellen E. Codd、Christopher M. Flores、Scott L. Dax
DOI:10.1016/j.bmcl.2007.09.036
日期:2007.11
We report on a series of alpha-substituted-beta-tetralin-derived and related phenethyl-based isoquinolinyl and hydroxynaphthyl ureas as potent antagonists of the human TRPV1 receptor. The synthesis and Structure-activity relationships (SAR) of the series are described. (C) 2007 Elsevier Ltd. All rights reserved.