Noradrenaline bitartrate monohydrate
| 规格 | 价格 | 货期 | 数量 |
|---|---|---|---|
| 1mL(10 mM in DMSO) | ¥454.00 | 现货 | |
| 500mg | ¥481.00 | 现货 | |
| 1g | ¥609.00 | 现货 | |
| 5g | ¥1818.00 | 现货 |
特色产品
- 用于免疫印迹和质谱分析等后续操作
- 适用于30 KDa-130 KDa大小的蛋白
- 可将信号灵敏度提高100倍
- 同时保持稳定的特异性和分辨率
- 提供更高的转录效率并抑制免疫激活
- 使用5-moUTP和Cy5-utp修饰
产品描述
Noradrenaline bitartrate monohydrate is an agonist of adrenergic receptors, with Ki values of 330, 56 and 740 nM for α1, α2 and β1 adrenoceptors, respectively [1].
Noradrenaline is a neurotransmitter distributed in both the peripheral and central nervous systems. In the autonomic nervous system, noradrenaline acting at α1-receptors causes constriction of cutaneous blood vessels. In the central nervous system, noradrenaline found primarily in the locus coeruleus in the brainstem, plays important roles in a variety of physiological activities, such as sleep/wake cycles, attention, orientation, mood and memory [2].
In femoral strips isolated from the untreated dogs, noradrenaline bitartrate monohydrate (5 × 10-9 ~ 10-4 M) induced dose-dependent contractions which were inhibited completely by 10-8 M phenoxybcnzamine administered 40 min previously. In the femoral strips isolated from the ephedrine-treated dogs, contractile responses to noradrenaline bitartrate monohydrate were potentiated at low concentrations (5 × 10-9 ~ 10-7 M) but inhibited at high concentrations (5 × 10-7 ~ 10-4 M) [3].
References:
[1]. Ramos B P, Arnsten A F. Adrenergic pharmacology and cognition: focus on the prefrontal cortex. Pharmacology & Therapeutics, 2007, 113(3): 523-536.
[2]. Bylund D B, Bylund K C. Norepinephrine. Encyclopedia of the Neurological Sciences (Second Edition), 2014, 3: 638–640.
[3]. Furukawa T, Morishita H. Modifications of responses to adrenergic drugs in arterial strip by treatment in vivo with ephedrine and reserpine. The Japanese Journal of Pharmacology, 1975, 25(4): 441-451.
产品性质
| 物理外观 | A solid |
| CAS号 | 108341-18-0 |
| 分子式 | C8H11NO3·C4H6O6·H2O |
| 分子量 | 337.28 |
| 小分子别名 | Norepinephrine bitartrate monohydrate |
| 化学名称 | (R)-4-(2-amino-1-hydroxyethyl)benzene-1,2-diol (2R,3R)-2,3-dihydroxysuccinate hydrate |
| 溶解度 | insoluble in EtOH; ≥11.35 mg/mL in DMSO; ≥51 mg/mL in H2O |
| SMILES | NC[C@@H](c(cc1)cc(O)c1O)O.O[C@H]([C@H](C(O)=O)O)C(O)=O.O |
| 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 | 重酒石酸去甲肾上腺素是一种直接刺激α-肾上腺素能受体的药物。 |



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