Synthesis and in vitro evaluation of novel coumarin–chalcone hybrids as potential anticancer agents

Show simple item record

dc.contributor.author Sashidhara, K V
dc.contributor.author Kumar, Abdhesh
dc.contributor.author Kumar, Manoj
dc.contributor.author Sarkar, Jayanta
dc.contributor.author Sinha, S
dc.date.accessioned 2011-05-13T08:38:55Z
dc.date.available 2011-05-13T08:38:55Z
dc.date.issued 2010
dc.identifier.citation Bioorganic & Medicinal Chemistry Letters, 20(24), 7205-7211 en
dc.identifier.uri http://hdl.handle.net/123456789/663
dc.description.abstract A series of coumarin-chalcone hybrids have been synthesized and evaluated for their in vitro cytotoxicity against a panel of four human cancer cell lines and normal fibroblasts (NIH3T3). Among 21 compounds screened, three compounds (23, 25 & 26) showed IC50 range in between 3.59 to 17.97 µM. The most promising compound 26 showed around 30 fold more selectivity towards C33A (cervical carcinoma) cells over normal fibroblast NIH3T3 cells with an IC50 value of 3.59 µM. en
dc.format.extent 207680 bytes
dc.format.mimetype application/pdf
dc.language.iso en en
dc.relation.ispartofseries CDRI Communication No 7961 en
dc.subject Synthesis en
dc.subject Coumarin en
dc.subject Chalcone en
dc.subject in vitro en
dc.subject Cytotoxicity en
dc.title Synthesis and in vitro evaluation of novel coumarin–chalcone hybrids as potential anticancer agents en
dc.type Article en


Files in this item

This item appears in the following Collection(s)

Show simple item record

Search DSpace


Advanced Search

Browse

My Account