购物车
- 全部删除
- 您的购物车当前为空
Bethanidine sulfate 和其邻位氯衍生物 (BW 392C60) 作为有效的肾上腺素能神经元阻滞剂,在多种动物模型中(特别是猫)展示了与溴苄胺及胍乙啶相似的拟交感神经效应。此化合物在神经刺激期抑制去甲肾上腺素的释放,并增加平滑肌对肾上腺素和去甲肾上腺素的敏感性。Bethanidine sulfate 能提高酪胺的升压反应,然而该效应随剂量增加而递减。不同于胍乙啶,Bethanidine sulfate 不消耗猫虹膜中的升压胺。它还会暂时抑制自主胆碱能系统,并在高剂量下造成短暂的神经肌肉麻痹,对比其持久的肾上腺素能神经阻断作用。
Bethanidine sulfate 和其邻位氯衍生物 (BW 392C60) 作为有效的肾上腺素能神经元阻滞剂,在多种动物模型中(特别是猫)展示了与溴苄胺及胍乙啶相似的拟交感神经效应。此化合物在神经刺激期抑制去甲肾上腺素的释放,并增加平滑肌对肾上腺素和去甲肾上腺素的敏感性。Bethanidine sulfate 能提高酪胺的升压反应,然而该效应随剂量增加而递减。不同于胍乙啶,Bethanidine sulfate 不消耗猫虹膜中的升压胺。它还会暂时抑制自主胆碱能系统,并在高剂量下造成短暂的神经肌肉麻痹,对比其持久的肾上腺素能神经阻断作用。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
10 mg | 询价 | 10-14周 | |
50 mg | 询价 | 10-14周 |
产品描述 | Bethanidine sulfate and its ortho-chloro derivative (BW 392C60) are potent adrenergic neuron blockers exhibiting sympathomimetic effects similar to those of bromobenzamine and guanethidine in various animal models, particularly in cats. These compounds inhibit the release of norepinephrine during neural stimulation and enhance the responsiveness of smooth muscle to epinephrine and norepinephrine. Notably, bethanidine sulfate increases the pressor response to tyramine, although this effect diminishes with higher doses. Unlike guanethidine, bethanidine sulfate does not deplete pressor amines in the iris of cats following administration. Additionally, it temporarily suppresses autonomic cholinergic mechanisms and can cause transient neuromuscular paralysis at large doses, contrasting its long-term adrenergic neuron blocking effects. |
别名 | BW 467C60 |
分子量 | 275.32 |
分子式 | C10H17N3O4S |
CAS No. | 114-85-2 |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
版权所有©2015-2024 TargetMol Chemicals Inc.保留所有权利.