S(-)-Propranolol HCl
S(-)-盐酸普萘洛尔是一种非选择性β-肾上腺素能受体(βAR)拮抗剂,对β1AR和β2AR具有高亲和力,其Ki值分别为1.8 nM和0.8 nM。盐酸普萘洛尔抑制[3H]-DHA与大鼠脑膜制备物的结合,其IC50为12 nM。
| Discription | S(-)-Propranolol Hydrochloride is a nonselective β-adrenergic receptor (βAR) antagonist, has high affinity for the β1AR and β2AR with Ki values of 1.8 nM and 0.8 nM, respectively. Propranolol hydrochloride inhibits [3H]-DHA binding to rat brain membrane preparation with an IC50 of 12 nM. |
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| 目录号 | A13428 |
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| 分子式 | C16H22ClNO2 |
| 分子量 | 295.8 |
| CAS号 | CAS: 4199-10-4 |
| SMILES | CC(C)NC[C@@H](COC1=CC=CC2=CC=CC=C21)O.Cl |
| 其他名称 | S-(-)-PROPANOLOL HCL, (S)-PROPRANOLOL HYDROCHLORIDE |
| 储存条件 | Store lyophilized at -20ºC, keep desiccated. |
Calculate the dilution required to prepare a stock solution. This equation is commonly abbreviated as: C1V1 = C2V2