Please use this identifier to cite or link to this item: http://10.9.150.37:8080/dspace//handle/atmiyauni/1707
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dc.contributor.authorKapadiya, K .-
dc.contributor.authorPandya, M.-
dc.contributor.authorRathod, C.-
dc.contributor.authorDhalani, J.-
dc.contributor.authorDhaduk, B.-
dc.date.accessioned2024-11-19T11:18:42Z-
dc.date.available2024-11-19T11:18:42Z-
dc.date.issued2018-
dc.identifier.citationKapadiya, K., Pandya, M., Rathod, C., Dhalani, J., & Dhaduk, B. (2018). Anti-cancer investigation of newly derived alicyclic ring and morpholine supported hybrid molecules by industrially viable route.en_US
dc.identifier.urihttp://10.9.150.37:8080/dspace//handle/atmiyauni/1707-
dc.description.abstractIn an attempt to design and synthesize a new class of anticancer molecules, we have reported coupling of aryl aldehyde, p-toluidine and morpholine based isocyanide with cyclopropane carboxylic acid to generate a small library of 08 compounds (5a-5h) by ugi multicomponent reaction in a single step manner. Structures of the newly synthesized compounds were recognized on the basis of spectral data i.e. 1H NMR, 13C NMR, IR and Mass. These compounds were screened for their anticancer activity against nine basic panels as well as NCI-60 cell-lines. In vitro anticancer studies revealed that the compound 5ashowed maximum potency against HCT-116 in colon cancer cell lines with GI50 values 46.27 µg/ml.en_US
dc.language.isoenen_US
dc.publisherJournal of Scientific & Industrial Researchen_US
dc.subjectCyclopropaneen_US
dc.subjectAnticancer Screeningen_US
dc.subjectUgi Multicomponent Reactionen_US
dc.subjectMorpholinoethyl Isocyanideen_US
dc.titleAnti-cancer Investigation of Newly Derived Alicyclic ring and Morpholine Supported Hybrid Molecules by Industrially viable Routeen_US
dc.typeArticleen_US
Appears in Collections:01. Journal Articles

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