Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10593044 | Bioorganic & Medicinal Chemistry Letters | 2013 | 4 Pages |
Abstract
In the last decade the inhibition of the enzyme 11β-hydroxysteroid dehydrogenase 1 (11β-HSD1) emerged as a promising new strategy to treat diabetes and several metabolic syndrome phenotypes. Using a molecular modeling approach and classical bioisosteric studies, we discovered a new class of 11β-HSD1 inhibitors bearing an arylsulfonylpiperazine scaffold. Optimization of the initial lead resulted in compound 11 that selectively inhibits 11β-HSD1 (IC50 = 0.7 μM).
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Sandra Hofer, Denise V. Kratschmar, Brigitte Schernthanner, Anna Vuorinen, Daniela Schuster, Alex Odermatt, Johnny Easmon,