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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/2936
Title: Synthesis of 3-phenylpyrazolopyrimidine-1,2,3-triazole conjugates and evaluation of their Src kinase inhibitory and anticancer activities
Authors: Kumar, Anil
Keywords: Chemistry
Anticancer activity
Click reaction
Phenylpyrazolopyrimidine
Src kinase
1,2,3-Triazole
Issue Date: Mar-2011
Publisher: Elsiever
Abstract: A series of two classes of 3-phenylpyrazolopyrimidine-1,2,3-triazole conjugates were synthesized using click chemistry approach. All compounds were evaluated for inhibition of Src kinase and human ovarian adenocarcinoma (SK-Ov-3), breast carcinoma (MDA-MB-361), and colon adenocarcinoma (HT-29). Hexyl triazolyl-substituted 3-phenylpyrazolopyrimidine exhibited inhibition of Src kinase with an IC50 value of 5.6 μM. 4-Methoxyphenyl triazolyl-substituted 3-phenylpyrazolopyrimidine inhibited the cell proliferation of HT-29 and SK-Ov-3 by 73% and 58%, respectively, at a concentration of 50 μM.
URI: https://www.sciencedirect.com/science/article/pii/S0960894X11000709?via%3Dihub
http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2936
Appears in Collections:Department of Chemistry

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