Bicyclo[2.2.2]octyltriazole inhibitors of 11β-hydoxysteroid dehydrogenase type 1. Pharmacological agents for the treatment of metabolic syndrome

Following the discovery of a metabolic ‘soft-spot’ on a bicyclo[2.2.2]octyltriazole lead, an extensive effort was undertaken to block the oxidative metabolism and improve PK of this potent HSD1 lead. In this communication, SAR survey focusing on various alkyl chain replacements will be detailed. Thi...

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Veröffentlicht in:Bioorganic & medicinal chemistry letters 2011-04, Vol.21 (8), p.2568-2572
Hauptverfasser: Maletic, Milana, Leeman, Aaron, Szymonifka, Michael, Mundt, Steven S., Zokian, Hratch J., Shah, Kashmira, Dragovic, Jasminka, Lyons, Kathy, Thieringer, Rolf, Vosatka, Anne H., Balkovec, James, Waddell, Sherman T.
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Sprache:eng
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Zusammenfassung:Following the discovery of a metabolic ‘soft-spot’ on a bicyclo[2.2.2]octyltriazole lead, an extensive effort was undertaken to block the oxidative metabolism and improve PK of this potent HSD1 lead. In this communication, SAR survey focusing on various alkyl chain replacements will be detailed. This effort culminated in the discovery of a potent ethyl sulfone inhibitor with an improved PK profile across species and improved physical properties. Following the discovery of a metabolic ‘soft-spot’ on a bicyclo[2.2.2]octyltriazole lead, an extensive effort was undertaken to block the oxidative metabolism and improve PK of this potent HSD1 lead. In this communication, SAR survey focusing on various alkyl chain replacements will be detailed. This effort culminated in the discovery of a potent ethyl sulfone inhibitor with an improved PK profile across species and improved physical properties.
ISSN:0960-894X
1464-3405
DOI:10.1016/j.bmcl.2011.01.018