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‘Bridged’ stilbene derivatives as selective cyclooxygenase-1 inhibitors
- 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]
- Subjects :
- *PHENYL compounds
*BIFONAZOLE
*LIGNANS
*METHADYL acetate
Subjects
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