'Bridged' stilbene derivatives as selective cyclooxygenase-1 inhibitors

被引:41
作者
Handler, Norbert
Brunhofer, Gerda
Studenik, Christian
Leisser, Klaus
Jaeger, Walter
Parth, Stephanie
Erker, Thomas
机构
[1] Univ Vienna, Dept Med Chem, A-1090 Vienna, Austria
[2] Univ Vienna, Dept Pharmacol & Toxicol, A-1090 Vienna, Austria
[3] Univ Vienna, Dept Clin Pharm & Diagnost, A-1090 Vienna, Austria
关键词
COX-inhibition; resveratrol; COX-1; stilbene; docking model;
D O I
10.1016/j.bmc.2007.06.030
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Resveratrol ((E)-3,4',5-ti-ihydroxy-stilbene), a phytoalexin found in various plants, shows non-selective cyclooxygenase-1 (COX-1) and cyclooxygenase-2 (COX-2) inhibition. In order to find more selective COX inhibitors a series of bridged stilbene derivatives was synthesized and evaluated for their ability to inhibit both COX- 1 and COX-2 in vitro. The compounds showed a high rate of COX-1 inhibition with the most potent compounds exhibiting submicromolar IC50 values and high selectivity indices. A prediction model for COX-inhibiting activity was also developed using the classical LIE approach resulting in consistent docking data for our molecule sample. Phenyl substituted 1,2-dihydronaphthalene derivatives and 1H-indene derivatives therefore represent a novel class of highly selective COX-1 inhibitors and land promising candidates for in vivo studies. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6109 / 6118
页数:10
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