Design, synthesis, and biological evaluation of (E)-N-aryl-2-arylethenesulfonamide analogues as potent and orally bioavailable microtubule-targeted anticancer agents.
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Novel Natural Product- and Privileged Scaffold-Based Tubulin Inhibitors Targeting the Colchicine Binding SiteDiscovery of 2-(1H-indol-5-ylamino)-6-(2,4-difluorophenylsulfonyl)-8-methylpyrido[2,3-d]pyrimidin-7(8H)-one (7ao) as a potent selective inhibitor of Polo like kinase 2 (PLK2).Evaluation of antimicrobial activity of glycinate and carbonate derivatives of cholesterol: Synthesis and characterization.Tubulin inhibitors targeting the colchicine binding site: a perspective of privileged structures.
P2860
Design, synthesis, and biological evaluation of (E)-N-aryl-2-arylethenesulfonamide analogues as potent and orally bioavailable microtubule-targeted anticancer agents.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 25 June 2013
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Design, synthesis, and biologi ...... le-targeted anticancer agents.
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Design, synthesis, and biologi ...... le-targeted anticancer agents.
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type
label
Design, synthesis, and biologi ...... le-targeted anticancer agents.
@en
Design, synthesis, and biologi ...... le-targeted anticancer agents.
@nl
prefLabel
Design, synthesis, and biologi ...... le-targeted anticancer agents.
@en
Design, synthesis, and biologi ...... le-targeted anticancer agents.
@nl
P2093
P2860
P356
P1476
Design, synthesis, and biologi ...... le-targeted anticancer agents.
@en
P2093
Amol Padgaonkar
Balaiah Akula
D R C Venkata Subbaiah
E Premkumar Reddy
E Vijaya Bharathi
James M Gallo
M V Ramana Reddy
Muralidhar R Mallireddigari
Stephen C Cosenza
P2860
P304
P356
10.1021/JM400575X
P407
P577
2013-06-25T00:00:00Z