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别名 维洛沙秦, Viloxazin, Emovit
Viloxazine (Viloxazin) (Viloxazin) 是一种去甲肾上腺素再摄取抑制剂、5-HT 2C 受体激动剂和 5-HT 2B 受体拮抗剂。其主要作用机制是调节血清素能和去甲肾上腺素能途径。Viloxazine通常用于抑郁症研究 [1] [2]。

Viloxazine (Viloxazin) (Viloxazin) 是一种去甲肾上腺素再摄取抑制剂、5-HT 2C 受体激动剂和 5-HT 2B 受体拮抗剂。其主要作用机制是调节血清素能和去甲肾上腺素能途径。Viloxazine通常用于抑郁症研究 [1] [2]。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 1 mg | ¥ 153 | 现货 | |
| 5 mg | ¥ 328 | 现货 | |
| 10 mg | ¥ 495 | 现货 | |
| 25 mg | ¥ 818 | 现货 | |
| 50 mg | ¥ 1,180 | 现货 | |
| 100 mg | ¥ 1,790 | 现货 | |
| 200 mg | ¥ 2,660 | 现货 | |
| 1 mL x 10 mM (in DMSO) | ¥ 363 | 现货 |
Viloxazine 相关产品
| 产品描述 | Viloxazine (Viloxazin) (Viloxazin) is a dual-action compound that functions as a norepinephrine reuptake inhibitor and exhibits potent agonistic activity towards 5-HT 2C receptors while acting as an antagonist for 5-HT 2B receptors, with respective potency values of EC 50 = 32 μM and IC 50 = 27 μM. Its primary mechanism of action involves the modulation of serotonergic and noradrenergic pathways. Viloxazine is commonly employed in depression research [1] [2]. |
| 靶点活性 | 5-HT2B:27 μM, 5-HT2C:32 μM(EC50) |
| 体内活性 | Viloxazine (1-16 mg/kg; spinal rat) stimulated the hind limb flexor reflex in the dose-dependent manner.[3] |
| 别名 | 维洛沙秦, Viloxazin, Emovit |
| 分子量 | 237.29 |
| 分子式 | C13H19NO3 |
| CAS No. | 46817-91-8 |
| Smiles | O(CC1CNCCO1)C2=C(OCC)C=CC=C2 |
| 存储 | Pure form: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| 溶解度信息 | DMSO: 60 mg/mL (252.86 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
| 体内实验配方 | 10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2.5 mg/mL (10.54 mM), Sonication is recommended. 请按顺序添加溶剂,在添加下一种溶剂之前,尽可能使溶液澄清。如有必要,可通过加热、超声、涡旋处理进行溶解。工作液建议现配现用。以上配方仅供参考,体内配方并不是绝对的,请根据不同情况进行调整。 | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
DMSO
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