Journal of Medicinal Chemistry · 2002 · 211 citations · 5 references
PharmacyMedicinal ChemistryPharmacologyDrug DesignDrug DiscoveryEnzymologyDiabetes ManagementDiabetes MellitusDiabetes PharmacotherapyEnzyme InhibitionLipid Metabolism11 Beta-hydroxysteroid DehydrogenaseAntidiabetic ActivityGluconeogenesisGluconeogenesis InhibitionHepatic GluconeogenesisHydroxysteroid DehydrogenasesMetabolic Enzyme InhibitionMurine Models
Novel antidiabetic arylsulfonamidothiazoles are presented that exert action through selective inhibition of the 11beta-hydroxysteroid dehydrogenase type 1 (11beta-HSD1) enzyme, thereby attenuating hepatic gluconeogenesis. The diethylamide derivative 2a was shown to potently inhibit human 11beta-HSD1 (IC(50) = 52 nM), whereas the N-methylpiperazinamide analogue 2b only inhibited murine 11beta-HSD1 (IC(50) = 96 nM). Both compounds showed >200-fold selectivity over human and murine 11beta-HSD2. 2b was subsequently shown to reduce glucose levels in diabetic KKA(y) mice, substantiating the 11beta-HSD1 enzyme as a target for the treatment of type 2 diabetes.
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Yuri Kotelevtsev, Megan C. Holmes, Ann N. Burchell et al. · Proceedings of the National Academy of Sciences · 1997 · 855 citations
Hypertension in mice lacking 11β-hydroxysteroid dehydrogenase type 2
Yuri Kotelevtsev, Roger Brown, Stewart Fleming et al. · Journal of Clinical Investigation · 1999 · 284 citations · Full text
Medicine, Endocrinology, Physiology +17
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