Abstract
A series of IAP antagonists based on thiazole or benzothiazole amide isosteres was designed and synthesized. These compounds were tested for binding to the XIAP-BIR3 and ML-IAP BIR using a fluorescence polarization assay. The most potent of these compounds, 19a and 33b, were found to have K(i)'s of 20-30 nM against ML-IAP and 50-60 nM against XIAP-BIR3.
2010 Elsevier Ltd. All rights reserved.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, U.S. Gov't, Non-P.H.S.
MeSH terms
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Amides / chemistry*
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Amides / pharmacology*
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Binding Sites
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Biomimetics
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Crystallography, X-Ray
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Humans
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Inhibitor of Apoptosis Proteins / antagonists & inhibitors*
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Inhibitor of Apoptosis Proteins / metabolism
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Models, Molecular
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Peptides / chemistry*
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Peptides / metabolism
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Thiazoles / chemistry*
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Thiazoles / pharmacology*
Substances
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Amides
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Inhibitor of Apoptosis Proteins
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Peptides
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Thiazoles