Synthesis and identification of α-cyano bis(indolyl)chalcones as novel anticancer agents

dc.contributor.authorKumar, Dalip
dc.date.accessioned2021-10-27T04:20:03Z
dc.date.available2021-10-27T04:20:03Z
dc.date.issued2014-11-15
dc.description.abstractMicrowave-assisted synthesis of 23 α-cyano bis(indolyl)chalcones (6a–w) and their in vitro anticancer activity against three human cancer cell lines have been discussed. Among the synthesized chalcones, compound 6n was found to be the most potent and selective against A549 lung cancer cell line (IC50 = 0.8 μM). In a preliminary mechanism of action studies some α-cyano bis(indolyl)chalcones were found to enhance tubulin polymerization suggesting these compounds could act as microtubule stabilizing agents.en_US
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0960894X14010415?via%3Dihub
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3035
dc.language.isoenen_US
dc.publisherElsieveren_US
dc.subjectChemistryen_US
dc.subjectBis(indole)en_US
dc.subjectMicrowave-assisted synthesisen_US
dc.subjectChalconesen_US
dc.titleSynthesis and identification of α-cyano bis(indolyl)chalcones as novel anticancer agentsen_US
dc.typeArticleen_US

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