Abstract
Two new families of human farnesyltransferase inhibitors 13a-m and 14a-d, based on a phenothiazine scaffold, were synthesized. Compounds 14a and 14b were the most promising inhibitors of human farnesyltransferase with IC(50) values of 0.7 and 0.6 μM, respectively.
Copyright © 2012 Elsevier Masson SAS. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Catalytic Domain
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Enzyme Activation / drug effects
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Enzyme Inhibitors / chemical synthesis*
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Enzyme Inhibitors / pharmacology*
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Farnesyltranstransferase / antagonists & inhibitors*
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Humans
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Inhibitory Concentration 50
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Models, Molecular
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Molecular Structure
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Phenothiazines / chemistry
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Phenothiazines / pharmacology
Substances
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Enzyme Inhibitors
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Phenothiazines
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Farnesyltranstransferase