Synthesis and biological analysis of benzazol-2-yl piperazine sulfonamides as 11β-hydroxysteroid dehydrogenase 1 inhibitors
Date Issued
2013-01-01
Author(s)
Hofer, Sandra
Kratschmar, Denise V.
Schernthanner, Brigitte
Vuorinen, Anna
Schuster, Daniela
Easmon, Johnny
DOI
10.1016/j.bmcl.2013.07.047
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).