Please use this identifier to cite or link to this item: http://10.1.7.192:80/jspui/handle/123456789/7209
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dc.contributor.authorThakor, Twara-
dc.contributor.authorSavjani, Jignasa-
dc.date.accessioned2016-11-26T04:32:41Z-
dc.date.available2016-11-26T04:32:41Z-
dc.date.issued2014-
dc.identifier.urihttp://hdl.handle.net/123456789/7209-
dc.descriptionInternational Journal of PharmTech Research, 6 (4); 2014:1397-1406en_US
dc.description.abstractPyrazole substituted coumarin derivatives were synthesised via multi-component reaction namely 3-(4-substituted phenyl)-1-phenyl-1H-pyrazole-4-carbaldehyde containing 4-hydroxy-2H-chromen-2-one and 4-methyl-2-oxo-2H-chromen-7-yl acetate by conventional synthetic route. The structure of the synthesised compounds was characterized by FTIR, Mass, 1H NMR spectral analysis. The synthesized compounds were screened for anticancer activity against the Lung cancer cell line (NCIH-522 cell line) using anticancer drug doxorubicin as a standard. Cell line studies revealed that compound 2-amino-4-(3-(4-chloro phenyl)-1-phenyl- 1H-pyrazol-4-yl)- 5-oxo-4, 5-dihydropyrano[3,2-c] chromene-3-carbonitrile found to be active against the lung cancer cell line as compared to doxorubicin.en_US
dc.publisherSphinx Knowledge Houseen_US
dc.relation.ispartofseriesIPFP0238-
dc.subjectCell line studyen_US
dc.subjectCoumarinen_US
dc.subjectDoxorubicinen_US
dc.subjectLung canceren_US
dc.subjectPyrazole.en_US
dc.titleSynthesis and Cell line study of Pyrazole Substituted Coumarin Derivativesen_US
dc.typeArticleen_US
Appears in Collections:Faculty Papers

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