CSIR Central

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

IR@CDRI: CSIR-Central Drug Research Institute, Lucknow

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Field Value
 
Creator Sashidhara, K V
Kumar, Abdhesh
Kumar, Manoj
Sarkar, Jayanta
Sinha, S
 
Date 2011-05-13T08:38:55Z
2011-05-13T08:38:55Z
2010
 
Identifier Bioorganic & Medicinal Chemistry Letters, 20(24), 7205-7211
http://hdl.handle.net/123456789/663
 
Description 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.
 
Format 207680 bytes
application/pdf
 
Language en
 
Relation CDRI Communication No 7961
 
Subject Synthesis
Coumarin
Chalcone
in vitro
Cytotoxicity
 
Title Synthesis and in vitro evaluation of novel coumarin–chalcone hybrids as potential anticancer agents
 
Type Article