Catalog No. C5580

Raceanisodamine

(别名:Racanisodamine; 消旋山莨菪碱)

α1肾上腺素受体的弱拮抗剂

Raceanisodamine
规格价格货期数量
250mg
¥347.00
现货
500mg
¥595.00
现货
1g
¥952.00
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CAS号:17659-49-3纯度:98.00%
仅用于科研,不用于诊疗。未经明确授权不得转售。
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EZ Cap™ Cy5 Firefly Luciferase mRNA (5-moUTP)
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用于观察mRNA运送,定位,翻译
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HotStart™ 2X Green qPCR Master Mix
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产品描述

Raceanisodamine is a weak antagonist of α1-adrenergic receptors [1].

The adrenergic receptors play an important role in modulating sympathetic nervous system activity as well as a site of action for many therapeutic agents. The α1-adrenergic receptors contain three types, termed as α1A-, α1B-, and α1D. The α1-adrenergic receptor plays an essential role in smooth muscle, growth, neurological, and cardiovascular function [2]. With the binding of the endogenous ligands, epinephrine and norepinephrine, the adrenergic receptors are the prime mediators of smooth muscle contraction and hypertrophic growth [2].

Raceanisodamine was a natural tropane alkaloid predominantly found in the roots of A. tanguticus. Raceanisodamine weakly antagonized the activity of α1-adrenoceptors and blocked WB-4101 and clonidine binding in brain membrane preparations with pKi values of 2.63 and 1.61, respectively [1]. Raceanisodamine showed antioxidant effects and protected against free radical-induced cellular damage [3].

References:
[1] Varma D R, Yue T L.  Adrenoceptor blocking properties of atropine‐like agents anisodamine and anisodine on brain and cardiovascular tissues of rats[J]. British journal of pharmacology, 1986, 87(3): 587-594.
[2] Piascik M T, Perez D M.  α1-Adrenergic receptors: new insights and directions[J]. Journal of Pharmacology and Experimental Therapeutics, 2001, 298(2): 403-410.
[3] Poupko J M, Baskin S I, Moore E.  The pharmacological properties of anisodamine[J]. Journal of Applied Toxicology, 2007, 27(2): 116-121.

产品性质

物理外观Solid
CAS号17659-49-3
分子式C17H23NO4
分子量305.37
小分子别名Racanisodamine
化学名称6-hydroxy-8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-hydroxy-2-phenylpropanoate
溶解度≥13.32 mg/mL in EtOH; ≥13.65 mg/mL in H2O; ≥51.3 mg/mL in DMSO
SMILESCN(C(C1)CC(C2)OC(C(CO)c3ccccc3)=O)C2C1O
存储条件-20°C
运输条件蓝冰

产品应用 (实验数据来自文献,APExBIO并未验证,仅供参考)

IC50和靶点

生物活性描述拉卡尼索达明是茴香胺的外消旋异构体之一;药理作用与茴香胺相似。拉卡尼索达明是一种非选择性毒蕈碱拮抗剂;用作控制近视的滴眼液成分。

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