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Tuaminoheptane原为一种鼻塞解除剂,属于交感神经兴奋剂和血管收缩剂。通过抑制和释放去甲肾上腺素的作用,Tuaminoheptane展现出其解充血和兴奋的效能。与具有芳香族环结构的苯乙胺类去甲肾上腺素释放剂不同,Tuaminoheptane的化学结构较为独特。此外,Tuaminoheptane还可能引起接触性皮炎,因其通过抑制体积调节阴离子通道而具有皮肤刺激性,这限制了其作为解充血剂的有效性。
Tuaminoheptane原为一种鼻塞解除剂,属于交感神经兴奋剂和血管收缩剂。通过抑制和释放去甲肾上腺素的作用,Tuaminoheptane展现出其解充血和兴奋的效能。与具有芳香族环结构的苯乙胺类去甲肾上腺素释放剂不同,Tuaminoheptane的化学结构较为独特。此外,Tuaminoheptane还可能引起接触性皮炎,因其通过抑制体积调节阴离子通道而具有皮肤刺激性,这限制了其作为解充血剂的有效性。
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 | Tuaminoheptane was originally developed as a nasal decongestant and belongs to the class of sympathomimetics and vasoconstrictors. It exhibits decongestant and stimulating effects by inhibiting and releasing norepinephrine. Unlike phenethylamine-based norepinephrine releasers, Tuaminoheptane has a unique chemical structure. Additionally, it may cause contact dermatitis due to its potential to irritate the skin by inhibiting volume-regulated anion channels, which limits its effectiveness as a decongestant. |
别名 | Tuamine sulfate |
分子量 | 164.26 |
分子式 | C7H17N 1/2H2O4S |
CAS No. | 6411-75-2 |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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