Discovery of orally active butyrolactam 11β-HSD1 inhibitors

Bioorganic & Medicinal Chemistry Letters
2006.0

Abstract

A series of metabolically stable butyrolactam 11beta-HSD1 inhibitors have been synthesized and biologically evaluated. These compounds exhibit excellent HSD1 potency and HSD2 selectivity, pharmacokinetic, and pharmacodynamic profiles.

Knowledge Graph

Similar Paper

Discovery of orally active butyrolactam 11β-HSD1 inhibitors
Bioorganic & Medicinal Chemistry Letters 2006.0
Synthesis, in Vitro Covalent Binding Evaluation, and Metabolism of <sup>14</sup>C-Labeled Inhibitors of 11β-HSD1
ACS Medicinal Chemistry Letters 2014.0
Discovery of SAR184841, a potent and long-lasting inhibitor of 11β-hydroxysteroid dehydrogenase type 1, active in a physiopathological animal model of T2D
Bioorganic &amp; Medicinal Chemistry Letters 2013.0
Discovery of 2-((R)-4-(2-Fluoro-4-(methylsulfonyl)phenyl)-2-methylpiperazin-1-yl)-N-((1R,2s,3S,5S,7S)-5-hydroxyadamantan-2-yl)pyrimidine-4-carboxamide (SKI2852): A Highly Potent, Selective, and Orally Bioavailable Inhibitor of 11β-Hydroxysteroid Dehydrogenase Type 1 (11β-HSD1)
Journal of Medicinal Chemistry 2016.0
Discovery of HSD-621 as a Potential Agent for the Treatment of Type 2 Diabetes
ACS Medicinal Chemistry Letters 2013.0
Design, Synthesis, Biological Evaluation and Pharmacokinetics of Bis(hydroxyphenyl) substituted Azoles, Thiophenes, Benzenes, and Aza-Benzenes as Potent and Selective Nonsteroidal Inhibitors of 17β-Hydroxysteroid Dehydrogenase Type 1 (17β-HSD1)
Journal of Medicinal Chemistry 2008.0
Design, Synthesis, and Biological Evaluation of (Hydroxyphenyl)naphthalene and -quinoline Derivatives: Potent and Selective Nonsteroidal Inhibitors of 17β-Hydroxysteroid Dehydrogenase Type 1 (17β-HSD1) for the Treatment of Estrogen-Dependent Diseases
Journal of Medicinal Chemistry 2008.0
New Drug-Like Hydroxyphenylnaphthol Steroidomimetics As Potent and Selective 17β-Hydroxysteroid Dehydrogenase Type 1 Inhibitors for the Treatment of Estrogen-Dependent Diseases
Journal of Medicinal Chemistry 2011.0
Discovery of novel dual functional agent as PPARγ agonist and 11β-HSD1 inhibitor for the treatment of diabetes
Bioorganic &amp; Medicinal Chemistry 2009.0
Discovery of a Potent, Orally Active 11β-Hydroxysteroid Dehydrogenase Type 1 Inhibitor for Clinical Study: Identification of (S)-2-((1S,2S,4R)-Bicyclo[2.2.1]heptan-2-ylamino)-5-isopropyl-5-methylthiazol-4(5H)-one (AMG 221)
Journal of Medicinal Chemistry 2010.0