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dc.contributor.authorNegi, Arvind
dc.contributor.authorAlex, Jimi Marin
dc.contributor.authorAmrutkar, Suyog M.
dc.contributor.authorBaviskar, Ashish T.
dc.contributor.authorJoshi, Gaurav
dc.contributor.authorSingh, Sandeep
dc.contributor.authorBanerjee, Uttam Chand
dc.contributor.authorKumar, Raj
dc.date.accessioned2019-03-22T09:20:38Z
dc.date.available2019-03-22T09:20:38Z
dc.date.issued2015
dc.identifier.citationNegi A., Alex J.M., Amrutkar S.M. et.al. (2015) Imine/amide-imidazole conjugates derived from 5-amino-4-cyano-N1-substituted benzyl imidazole: Microwave-assisted synthesis and anticancer activity via selective topoisomerase-II-? inhibitionen_US
dc.identifier.issn9680896
dc.identifier.urihttp://kr.cup.edu.in/handle/32116/2098
dc.description.abstractMicrowave-accelerated synthesis and anticancer activity of novel imine/amide-imidazole conjugates derived from 5-amino-4-cyano-N1-substituted benzyl imidazole against a panel of seven cancer cell lines are reported for the first time. Compounds ARK-4, 10 and 12 in the series show promising in vitro anti proliferative activity with low micromolar IC 50 values against A-459 (lung), Hep-G2 (liver) and H-460 (liver) cancer cell lines. Compounds caused the increase in ROS levels as well as mitochondrial membrane depolarization, which might induce apoptosis. Further, mechanistic interventions on biological and molecular modeling data supported that compounds inhibited topoisomerase-II selectively.- 2015 Elsevier Ltd. All rights reserved.en_US
dc.language.isoenen_US
dc.publisherElsevier Ltden_US
dc.subjectAnticancer activityen_US
dc.subjectAntioxidant activityen_US
dc.subjectImine/amide-imidazoleen_US
dc.subjectMolecular modelingen_US
dc.subjectTopoisomerase inhibitionen_US
dc.titleImine/amide-imidazole conjugates derived from 5-amino-4-cyano-N1-substituted benzyl imidazole: Microwave-assisted synthesis and anticancer activity via selective topoisomerase-II-? inhibitionen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.bmc.2015.07.020
dc.title.journalBioorganic and Medicinal Chemistry


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