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‘Bridged’ stilbene derivatives as selective cyclooxygenase-1 inhibitors

Authors :
Handler, Norbert
Brunhofer, Gerda
Studenik, Christian
Leisser, Klaus
Jaeger, Walter
Parth, Stephanie
Erker, Thomas
Source :
Bioorganic & Medicinal Chemistry. Sep2007, Vol. 15 Issue 18, p6109-6118. 10p.
Publication Year :
2007

Abstract

Abstract: Resveratrol ((E)-3,4′,5-trihydroxy-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. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
09680896
Volume :
15
Issue :
18
Database :
Academic Search Index
Journal :
Bioorganic & Medicinal Chemistry
Publication Type :
Academic Journal
Accession number :
25935394
Full Text :
https://doi.org/10.1016/j.bmc.2007.06.030