MF-438 is a potent and orally bioavailable stearoyl-CoA desaturase 1 (SCD1) inhibitor with an IC50 of 2.3 nM for rSCD1
靶点:
EC50: 2.3 nM (rSCD1)
体内研究:
MF-438 exhibits an ED50 between 1 and 3 mg/kg in a mouse model.
参考文献:
1. Léger S, et al. Synthesis and biological activity of a potent and orally bioavailable SCD inhibitor (MF-438). Bioorg Med Chem Lett. 2010 Jan 15;20(2):499-502.