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Synthesis of sulfonamides and evaluation of their histone deacetylase (HDAC) activity. Molecules 2007, 12, 1125-1135. © 2009 by the authors; licensee Molecular Diversity Preservation International

By Seikwan Oh

Abstract

Abstract: A simple synthesis of sulfonamides 4–22 as novel histone deacetylase (HDAC) inhibitors is described. The key synthetic strategies involve N–sulfonylation of L–proline benzyl ester hydrochloride (2) and coupling reaction of N–sulfonyl chloride 3 with amines in high yields. It was found that several compounds showed good cellular potency with the most potent compound 20 exhibiting an IC50 = 2.8 µM in vitro

Topics: HDAC, N–Sulfonylation, Coupling reaction, Anticancer
Year: 2014
OAI identifier: oai:CiteSeerX.psu:10.1.1.411.9259
Provided by: CiteSeerX
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