Discovery of potent, selective, orally bioavailable stearoyl-CoA desaturase 1 inhibitors - PubMed (original) (raw)
. 2007 Jun 28;50(13):3086-100.
doi: 10.1021/jm070219p. Epub 2007 May 27.
John K Lynch, Jennifer Freeman, Bo Liu, Zhili Xin, Hongyu Zhao, Michael D Serby, Philip R Kym, Tom S Suhar, Harriet T Smith, Ning Cao, Ruojing Yang, Rich S Janis, Joel A Krauser, Steven P Cepa, David W A Beno, Hing L Sham, Christine A Collins, Teresa K Surowy, Heidi S Camp
Affiliations
- PMID: 17530838
- DOI: 10.1021/jm070219p
Discovery of potent, selective, orally bioavailable stearoyl-CoA desaturase 1 inhibitors
Gang Liu et al. J Med Chem. 2007.
Abstract
Stearoyl-CoA desaturase 1 (SCD1) catalyzes the committed step in the biosynthesis of monounsaturated fatty acids from saturated, long-chain fatty acids. Studies with SCD1 knockout mice have established that these animals are lean and protected from leptin deficiency-induced and diet-induced obesity, with greater whole body insulin sensitivity than wild-type animals. In this work, we have discovered a series of potent, selective, orally bioavailable SCD1 inhibitors based on a known pyridazine carboxamide template. The representative lead inhibitor 28c also demonstrates excellent cellular activity in blocking the conversion of saturated long-chain fatty acid-CoAs (LCFA-CoAs) to monounsaturated LCFA-CoAs in HepG2 cells.
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