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D4R antagonist-2 是有效的、选择性的D4R 拮抗剂(IC50= 6.87 μM)。 D4R antagonist-2 显示有利的体外 PK 参数以及较好的脑渗透性。 D4R antagonist-2 在帕金森病中有研究价值。
D4R antagonist-2 是有效的、选择性的D4R 拮抗剂(IC50= 6.87 μM)。 D4R antagonist-2 显示有利的体外 PK 参数以及较好的脑渗透性。 D4R antagonist-2 在帕金森病中有研究价值。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 25 mg | ¥ 10,600 | 10-14周 | |
| 50 mg | ¥ 13,800 | 10-14周 | |
| 100 mg | ¥ 17,500 | 10-14周 |
D4R antagonis-2 相关产品
| 产品描述 | D4R antagonist-2 is a potent and selective D4R antagonist (IC50= 6.52 μM). D4R antagonist-2 displays favorable in vitro PK parameters and exhibits good brain penetration. D4R antagonist-2 has the research potential in Parkinson’s disease. |
| 靶点活性 | D4 Receptor:6.87 μM |
| 体外活性 | D4R antagonist-2 (compound 11a) shows good activity with an K i of 299.4 nM [1]. |
| 体内活性 | D4R antagonist-2 displays very favorable in vitro PK parameters and is brain pentrent (K p =2.9) [1]. b>Pharmacokinetic Parameters of D4R antagonist-2 in rats [1]. rat cassette (0.25 mpk) 11a CL (ml/min/kg) 22.0 T 1/2 (h) 4.4 C 0 (ng/ml) 91 V ss (L/kg) 5.5 AUC (h*ng/mL) 747 Animal Model: rats [1] Dosage: Administration: i.v. Result: Displayed very favorable in vitro PK parameters and was brain pentrent (K p =2.9). |
| 分子量 | 408.87 |
| 分子式 | C21H23ClF2N2O2 |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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