溶解性 | DMSO 93 mg/mL (199.03 mM); Water <1 mg/mL (<1 mM); Ethanol <1 mg/mL (<1 mM) |
存贮条件 | 储存温度-20°C |
产品介绍 | MK-8245是一种靶向作用于肝脏的stearoyl-CoA desaturase (SCD)(硬脂酰辅酶A去饱和酶)抑制剂,作用于人类SCD1时,IC50为1 nM,作用于大鼠和小鼠SCD1时,IC50为3 nM,具有抗糖尿病和抗高脂血症作用。Phase 2。 |
备注 | MK-8245 is an liver-targeting inhibitor of stearoyl-CoA desaturase (SCD) with IC50 of 1 nM for human SCD1 and 3 nM for both rat SCD1 and mouse SCD1, with anti-diabetic and anti-dyslipidemic efficacy. Phase 2. |
别名 | 5-[3-[4-(2-溴-5-氟苯氧基)-1-哌啶基]-5-异恶唑基]-2H-四氮唑-2-乙酸;MK 8245;MK8245;5-[3-[4-(2-Bromo-5-fluorophenoxy)-1-piperidinyl]-5-isoxazolyl]-2H-tetrazole-2-acetic acid |