Synthesis of novel ciprofloxacin analogues and evaluation of their anti-proliferative effect on human cancer cell lines

dc.contributor.authorKumar, Anil
dc.date.accessioned2021-10-17T13:58:46Z
dc.date.available2021-10-17T13:58:46Z
dc.date.issued2013
dc.description.abstractA series of twenty two novel 1-cyclopropyl-6-fluoro-4-oxo-7-(4-substituted piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid analogues have been synthesized, characterized (1H NMR, 13C NMR and LCMS) and evaluated for their inhibitory activity on the proliferation of human caucasian acute lymphoblastic leukemia cells (CCRF-CEM), breast adenocarcinoma cells (MDA-MB-468) and human colon carcinoma cells (HCT-116). Among all the synthesized ciprofloxacin analogues 3t at 50 μM showed comparable potency to doxorubicin (10 μM) in all three cell lines and 3j inhibited proliferation of MDA-MB-468 up to 35% selectively over other two cell lines.en_US
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0960894X13011517?via%3Dihub
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2890
dc.language.isoenen_US
dc.publisherElsieveren_US
dc.subjectChemistryen_US
dc.subjectSynthesisen_US
dc.subjectCiprofloxacin analoguesen_US
dc.subjectAnti-proliferativeen_US
dc.titleSynthesis of novel ciprofloxacin analogues and evaluation of their anti-proliferative effect on human cancer cell linesen_US
dc.typeArticleen_US

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