Abstract
A new series of cyclic sulfonamide derivatives was synthesized and evaluated for their ability to inhibit 11beta-HSD1. Cyclic sulfonamides with phenylacetyl substituents at the 2-position showed nanomolar inhibitory activities. Among them, compound 4e exhibited a good in vitro inhibitory activity and selectivity toward human 11beta-HSD2.
Copyright (c) 2009 Elsevier Ltd. All rights reserved.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
MeSH terms
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11-beta-Hydroxysteroid Dehydrogenase Type 1 / antagonists & inhibitors*
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11-beta-Hydroxysteroid Dehydrogenase Type 1 / metabolism
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Animals
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Cell Line
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Drug Discovery / methods*
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Humans
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Mice
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Microsomes / drug effects
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Microsomes / enzymology
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Sulfonamides / chemical synthesis*
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Sulfonamides / metabolism
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Sulfonamides / pharmacology
Substances
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Sulfonamides
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11-beta-Hydroxysteroid Dehydrogenase Type 1