A939572 (Synonyms: SCD1 Inhibitor, Stearoyl-CoA Desaturase 1 Inhibitor) |
| カタログ番号GC15921 |
A939572 は、mSCD1 および hSCD1 に対してそれぞれ <4 nM および 37 nM の IC50 値を持つ、強力な経口投与可能なステアロイル CoA デサチュラーゼ 1 (SCD1) 阻害剤です。
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Cas No.: 1032229-33-6
Sample solution is provided at 25 µL, 10mM.
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A939572 is a potent and orally bioavailable inhibitor of stearoyl-CoA desaturase1 (SCD1) with IC50 value of 37nM [1].
SCD is a microsomal enzyme that catalyzes the biosynthesis of monounsaturated fatty acids. One member of SCD family, SCD1, is regulated by dietary and hormonal factors and is proved to play an important role in lipid metabolism and body weight control. Thus, SCD1 is a target for the treatment of obesity and diabetes. A939572 is a synthetic inhibitor of SCD1 with improved inhibitory activity and lipophilicity than its parent compound. It shows inhibition of mouse SCD1 and human SCD1 with IC50 values of <4nM and 37nM, respectively. In addition, A939572 has no inhibitory activity to the co-enzymes of SCD1, cytochrome b5 and cytochrome b5 reductase. It suggests that A939572 interacts with SCD1 directly and specifically. Furthermore, A939572 shows high oral bioavailability in mice [1].
References:
[1] Xin Z, Zhao H, Serby M D, et al. Discovery of piperidine-aryl urea-based stearoyl-CoA desaturase 1 inhibitors. Bioorganic & medicinal chemistry letters, 2008, 18(15): 4298-4302.
Average Rating: 5 (Based on Reviews and 32 reference(s) in Google Scholar.)
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