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First synthesis and in vitro biological assessment of isosideroxylin,6,8-dimethylgenistein and their analogues as nitric oxide production inhibition agents
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作者 Jong-Woon Jung Kongara Damodar +1 位作者 Jin-Kyung Kim Jong-Gab Jun 《Chinese Chemical Letters》 SCIE CAS CSCD 2017年第5期1114-1118,共5页
A modular and efficient synthesis of the biologically significant C-methylisoflavones isosideroxylin(1),6,8-dimethylgenistein(2) and their analogues(3-8) is established for the first time.The synthesis is realiz... A modular and efficient synthesis of the biologically significant C-methylisoflavones isosideroxylin(1),6,8-dimethylgenistein(2) and their analogues(3-8) is established for the first time.The synthesis is realized in 7-8 steps in overall yields of 16%-24%from commercially inexpensive phloroglucinol and features a high yielding Vilsmeier-Haack reaction,Friedel-Crafts acylation,Gammill's protocol and Suzuki coupling as the pivotal transformations.Next,these compounds evaluated for their inhibitory potency on the production of nitric oxide(NO) in lipopolysaccharide(LPS)-activated RAW-264.7 cells as an indicator of anti-inflammatory activity.The results showed that all the compounds decreased NO production in a dose-dependent manner without marked cytotoxicity and IC_(50) values are found in the range of 10.17-33.88 μmol/L.Of note,compounds 3 followed by 1,7 and 8 show comparable inhibitory activity with positive control(N-monomethyl-L-arginine,L-NMMA). 展开更多
关键词 isosideroxylin 6 8-Dimethylgenistein Vilsmeier-Haack reaction Suzuki coupling Nitric oxide(NO) Anti-inflammatory
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