Synthesis and evaluation of diarylthiazole derivatives that inhibit activation of sterol regulatory element-binding proteins
- J Med Chem. 2011 Jul 14;54(13):4923-7. doi: 10.1021/jm200304y.
- 1. Institute for Chemical Research, Kyoto University, Uji, Kyoto, Japan.
Fatostatin, a recently discovered small molecule that inhibits activation of sterol regulatory element-binding protein (SREBP), blocks biosynthesis and accumulation of fat in obese mice. We synthesized and evaluated a series of fatostatin derivatives. Our structure-activity relationships led to the identification of N-(4-(2-(2-propylpyridin-4-yl)thiazol-4-yl)phenyl)methanesulfonamide (24, FGH10019) as the most potent druglike molecule among the analogues tested. Compound 24 has high aqueous solubility and membrane permeability and may serve as a seed molecule for further development.
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Cat. No.Product NameDescriptionTargetResearch Area
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target: Fatty Acid Synthase (FASN)Research Areas: Metabolic Disease