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Imarikiren(又名TAK-272)是一种高效、选择性强且可口服的直接肾素抑制剂,主要用于治疗糖尿病肾病。在hPRA检测中,TAK-272对人肾素的抑制活性极强(IC50 = 2.1 nM),并且对其他天冬酰胺蛋白酶如胃蛋白酶(IC50 > 10 μM)和组织蛋白酶D(IC50 > 10 μM)具有优异的选择性。在大鼠中,TAK-272展示了显著改善的PK形态(F = 25.2%)。通过口服给药(3 和 10 mg/kg),TAK-272展现了剂量依赖性的强效持久的降压效果。目前,TAK-272 HCl正处于人类临床试验阶段。
Imarikiren(又名TAK-272)是一种高效、选择性强且可口服的直接肾素抑制剂,主要用于治疗糖尿病肾病。在hPRA检测中,TAK-272对人肾素的抑制活性极强(IC50 = 2.1 nM),并且对其他天冬酰胺蛋白酶如胃蛋白酶(IC50 > 10 μM)和组织蛋白酶D(IC50 > 10 μM)具有优异的选择性。在大鼠中,TAK-272展示了显著改善的PK形态(F = 25.2%)。通过口服给药(3 和 10 mg/kg),TAK-272展现了剂量依赖性的强效持久的降压效果。目前,TAK-272 HCl正处于人类临床试验阶段。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
10 mg | 待询 | 10-14周 | |
50 mg | 待询 | 10-14周 |
产品描述 | Imarikiren (also known as TAK-272) is a potent, highly selective, orally bioavailable direct renin inhibitor primarily used for treating diabetic nephropathy. In hPRA assays, TAK-272 exhibits strong inhibitory activity against human renin (IC50 = 2.1 nM) and demonstrates excellent selectivity over other aspartic proteases such as pepsin (IC50 > 10 μM) and cathepsin D (IC50 > 10 μM). In rats, TAK-272 shows significantly improved pharmacokinetic properties (F = 25.2%) and, upon oral administration (3 and 10 mg/kg), exhibits a dose-dependent, potent, and sustained antihypertensive effect. Currently, TAK-272 HCl is undergoing human clinical trials. |
别名 | TAK-272 free base, (+)-, TAK-272 free base, 01IC75R817 |
分子量 | 499.65 |
分子式 | C27H41N5O4 |
CAS No. | 1202265-63-1 |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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