Please use this identifier to cite or link to this item: https://idr.l3.nitk.ac.in/jspui/handle/123456789/13269
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dc.contributor.authorPanathur, N.-
dc.contributor.authorGokhale, N.-
dc.contributor.authorUdayakumar, D.-
dc.contributor.authorKoushik, P.V.-
dc.contributor.authorYogeeswari, P.-
dc.contributor.authorSriram, D.-
dc.date.accessioned2020-03-31T08:45:30Z-
dc.date.available2020-03-31T08:45:30Z-
dc.date.issued2016-
dc.identifier.citationMedicinal Chemistry Research, 2016, Vol.25, 1, pp.135-148en_US
dc.identifier.urihttps://idr.nitk.ac.in/jspui/handle/123456789/13269-
dc.description.abstractA series of pyridazino[4,5-b]indole derivatives containing alkyl-, benzyl- and phenacyl-substituted 1,2,3-triazolylmethyl units was synthesized using click chemistry approach. All 30 compounds of the series were screened in vitro against four cancer cell lines, viz. breast cancer cells MDA-MB-231 and MCF 7, human primary glioblastoma U-87 and human neuroblastoma IMR-32 cell lines. Most of the compounds exhibited potent cancer cell growth inhibition activity at very low micromolar concentrations. The IC50 value of compounds 7v and 7x against human neuroblastoma IMR-32 cell line is 0.07 and 0.04 ?M, respectively. Among the tested compounds, ten compounds showed IC50 value less than 1 ?M against MDA-MB-231 cells, whereas against IMR-32 cells, nine compounds and, against U-87 cells, six compounds showed similar inhibition activity. Further, these molecules exhibited prominent binding affinity and docking scores in the molecular simulation study with the target enzyme PI3 kinase. Graphical Abstract: This paper illustrates the synthesis of new fused indole-pyridazinone derivatives containing substituted 1,2,3-triazoles via click chemistry approach. Most of the compounds exhibited potent cancer cell growth inhibition activity at very low micromolar concentrations. [Figure not available: see fulltext.] 2015 Springer Science+Business Media New York.en_US
dc.titleSynthesis of novel 5-[(1,2,3-triazol-4-yl)methyl]-1-methyl-3H-pyridazino[4,5-b]indol-4-one derivatives by click reaction and exploration of their anticancer activityen_US
dc.typeArticleen_US
Appears in Collections:1. Journal Articles

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