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Propranolol hydrochloride 是非选择性的β-adrenergic receptor 拮抗剂,对 β1AR 和 β2AR 具有高亲和力。它能够抑制 [3H]-DHA 与大鼠脑膜制剂的结合。它可以用于研究高血压,嗜铬细胞瘤,心肌梗塞,心律不齐,心绞痛和肥大心肌病。
Propranolol hydrochloride 是非选择性的β-adrenergic receptor 拮抗剂,对 β1AR 和 β2AR 具有高亲和力。它能够抑制 [3H]-DHA 与大鼠脑膜制剂的结合。它可以用于研究高血压,嗜铬细胞瘤,心肌梗塞,心律不齐,心绞痛和肥大心肌病。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
50 mg | ¥ 271 | 待询 | |
100 mg | ¥ 375 | 待询 | |
500 mg | ¥ 587 | 待询 | |
1 g | ¥ 970 | 待询 | |
1 mL x 10 mM (in DMSO) | ¥ 418 | 待询 |
Propranolol hydrochloride 相关产品
产品描述 | Propranolol hydrochloride is a widely used non-cardioselective beta-adrenergic antagonist. Propranolol has been used for MYOCARDIAL INFARCTION; ARRHYTHMIA; ANGINA PECTORIS; HYPERTENSION; HYPERTHYROIDISM; MIGRAINE; PHEOCHROMOCYTOMA; and ANXIETY but adverse effects instigate replacement by newer drugs. |
靶点活性 | β-adrenoceptor:12 nM |
体外活性 | In cultured endothelial or tumor cells, propranolol has been shown to both reduce cAMP levels and simultaneously activate the mitogen-activated protein kinase (MAPK) pathway downstream of βAR inhibition[2]. It displays high affinity for 5-HT1B receptors (Ki= 17 nM), and milder affinity for 5HT1D receptors (Ki= 10.2 μM)[3]. |
体内活性 | Chronic administration of propranolol increased the beta(1)-adrenoceptors but decreased the beta(2)-adrenoceptors without changing total amount of plasma membrane beta-adrenoceptors[4]. |
别名 | 盐酸普萘洛尔, Propranolol HCl, NCS-91523, ICI-45520, AY-64043 |
分子量 | 295.804 |
分子式 | C16H22ClNO2 |
CAS No. | 318-98-9 |
Smiles | Cl.CC(C)NCC(O)COc1cccc2ccccc12 |
密度 | no data available |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | ||||||||||||||||||||||||||||||||||||||||
溶解度信息 | DMSO: 55 mg/mL (185.93 mM), Sonication is recommended. Ethanol: <1 mg/mL H2O: 6 mg/mL (20.28 mM), Sonication is recommended. | ||||||||||||||||||||||||||||||||||||||||
溶液配制表 | |||||||||||||||||||||||||||||||||||||||||
H2O/DMSO
DMSO
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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。
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