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1135278-41-9

中文名称 SR 59230A HCl
英文名称 SR 59230A HCl
CAS 1135278-41-9
分子式 C21H27NO2.HCl
分子量 361.91
MOL 文件 1135278-41-9.mol
1135278-41-9 结构式 1135278-41-9 结构式

基本信息

中文别名
化合物 T13016L
SR 59230A盐酸盐
英文别名
SR-59230A hydrochloride,SR59230A hydrochloride

物理化学性质

储存条件Store at 4°C
溶解度溶于二甲基亚砜
形态固体
颜色白色

常见问题列表

生物活性
SR59230A hydrochloride 是一种有效,选择性的,可透过血脑屏障的 β3-肾上腺素能受体 (β3-adrenergic receptor) 拮抗剂,对 β3,β1 和 β2 受体的 IC50 分别为 40、408 和 648 nM。
靶点

IC50: 40 nM (β3 receptor), 408 nM ((β1 receptor), 648 nM (β2 receptor)

体外研究

SR59230A (100 nM-50 μM; 24 hours) is able to reduce cell viability in a dose-dependent manner in Neuro-2A, BE(2)C and SK-N-BE(2) NB cell lines.

Cell Viability Assay

Cell Line: Three different neuroblastoma (NB) cell lines, one murine (Neuro-2A) and two human (SK-N-BE(2), BE(2)C)
Concentration: 100 nM, 1 μM, 5 μM, 10 μM, and 50 μM
Incubation Time: 24 hours
Result: Reduced cell viability in a dose-dependent manner, with significant effect at a concentration limit over 1 µM for Neuro-2A cells and 5 µM for SK-N-BE(2) and BE(2)C).
体内研究

MDMA (20 mg/kg) produces a slowly developing hyperthermia, reaching a maximum increase of 1.8°C at 130 min post injection. SR59230A (0.5 mg/kg) produces a small but significant attenuation of the slowly developing hyperthermia to MDMA. SR59230A (5 mg/kg) reveals a significant and marked early hypothermic reaction to MDMA.

Animal Model: Male C-57BL6J wild-type mice (22-35 g)
Dosage: 0.5 or 5 mg/kg
Administration: Injected s.c.; administered 30 min prior to the injection s.c. of MDMA (20 mg/kg).
Result: Modulated the actions of MDMA on temperature involve α1-adrenoceptor antagonism.
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