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Bopindolol 是一种口服活性的 β-肾上腺素受体 (ARs) 拮抗剂,具有部分激动剂活性。Bopindolol 对 β1- 和 β2-ARs 无选择性,对β3-AR 亚型亲和力低。Bopindolol 是 Pindolol 的前体药物,可迅速代谢为活性水解形式。Bopindolol 可用于原发性和肾血管性高血压的研究。

Bopindolol 是一种口服活性的 β-肾上腺素受体 (ARs) 拮抗剂,具有部分激动剂活性。Bopindolol 对 β1- 和 β2-ARs 无选择性,对β3-AR 亚型亲和力低。Bopindolol 是 Pindolol 的前体药物,可迅速代谢为活性水解形式。Bopindolol 可用于原发性和肾血管性高血压的研究。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 25 mg | ¥ 10,600 | 6-8周 | |
| 50 mg | ¥ 13,800 | 6-8周 | |
| 100 mg | ¥ 17,500 | 6-8周 |
| 产品描述 | Bopindolol is an orally active antagonist of β-adrenoceptors (ARs) with partial agonist activity. Bopindolol is non-selective for β1- and β2-ARs and has low affinity for β3-AR subtype. Bopindolol is a prodrug of pindolol and can be rapidly metabolized to an active hydrolyzed form. Bopindolol can be used for essential and renovascular hypertension research [1] [2]. |
| 体内活性 | Bopindolol (intravenous injection; l8, 16 and 32 μg/kg) dose-dependently inhibits isoprenaline-induced tachycardia, and this agent is 4 times more potent than propranolol in anaesthetised dogs [1]. Bopindolol (intraperitoneal injection; 3.0 mg/kg) reduces the diastolic blood pressure (DBP) in pithed rats. And pindolol (1.0 mg/kg) produces similar decreases in DBP of about 8 mmHg. it also produces a dose-dependent decrease in heart rate [2]. |
| 分子量 | 380.48 |
| 分子式 | C23H28N2O3 |
| CAS No. | 62658-63-3 |
| Smiles | O(CC(OC(=O)C1=CC=CC=C1)CNC(C)(C)C)C2=C3C(NC(C)=C3)=CC=C2 |
| 密度 | 1.143 g/cm3 (Predicted) |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。
对于不同动物的给药剂量换算,您也可以参考 更多