Synthesis and in vitro anti-proliferative effects of 3-(hetero)aryl substituted 3-[(prop-2-ynyloxy)(thiophen-2-yl)methyl]pyridine derivatives on various cancer cell lines

dc.contributor.author Reddy Chamakura, Upendar
dc.contributor.author Sailaja, E.
dc.contributor.author Dulla, Balakrishna
dc.contributor.author Kalle, Arunasree M.
dc.contributor.author Bhavani, S.
dc.contributor.author Rambabu, D.
dc.contributor.author Kapavarapu, Ravikumar
dc.contributor.author Rao, M. V.Basaveswara
dc.contributor.author Pal, Manojit
dc.date.accessioned 2022-03-27T01:02:00Z
dc.date.available 2022-03-27T01:02:00Z
dc.date.issued 2014-03-01
dc.description.abstract A series of 3-(hetero)aryl substituted 3-[(prop-2-ynyloxy)(thiophen-2-yl) methyl]pyridine derivatives were designed as potential anticancer agents. These compounds were conveniently prepared by using Pd/C-Cu mediated Sonogashira type coupling as a key step. Many of these compounds were found to be promising when tested for their in vitro anti-proliferative properties against six cancer cell lines. All these compounds were found to be selective towards the growth inhibition of cancer cells with IC50 values in the range of 0.9-1.7 μM (against MDA-MB 231 and MCF7 cells), comparable to the known anticancer drug doxorubicin. © 2014 Elsevier Ltd. All rights reserved.
dc.identifier.citation Bioorganic and Medicinal Chemistry Letters. v.24(5)
dc.identifier.issn 0960894X
dc.identifier.uri 10.1016/j.bmcl.2014.01.044
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/S0960894X14000742
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/3925
dc.subject Alkyne
dc.subject Anti-proliferation
dc.subject Cancer
dc.subject Coupling
dc.subject Pd/C
dc.title Synthesis and in vitro anti-proliferative effects of 3-(hetero)aryl substituted 3-[(prop-2-ynyloxy)(thiophen-2-yl)methyl]pyridine derivatives on various cancer cell lines
dc.type Journal. Article
dspace.entity.type
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