149281-19-6
![149281-19-6 结构式](https://img.chemicalbook.com/CAS/20180808/GIF/149281-19-6.gif)
149281-19-6 性质
沸点 | 627.0±55.0 °C(Predicted) |
---|---|
密度 | 1.118±0.06 g/cm3(Predicted) |
储存条件 | Store at -20°C |
溶解度 | 溶于二甲基亚砜 |
酸度系数(pKa) | 12.88±0.60(Predicted) |
149281-19-6 用途与合成方法
IC50: 36 nM (rat 5 alpha reductase), 262 nM (human 5 alpha reductase)
CGP-53153 competitively inhibits rat microsomal 5 alpha reductase from prostate with an IC 50 of 36 nM compared to the reference compound finasteride (IC 50 =11 nM). CGP 53153 is approximately one order of magnitude more potent in inhibiting rat compared to human 5 alpha reductase, with IC 50 values of 36 and 262 nM, respectively
CGP-53153 can significantly reduce T-propionate-mediated prostate growth at oral doses of 0.01 mg/kg. CGP-53153 significantly reduces prostate weight at 3 and 10 mg/kg by 31% and 37%, respectively. Treatment for 12 weeks with both CGP-53153 reduces prostate volume by more than 70% in individual dogs. Neither body weight nor the weight of any organ tested is affected by CGP-53153.