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首页-小分子抑制剂&激动剂-Membrane Transporter/Ion Channel-Sodium Channel-VX-150
VX-150

Chemical Structure : VX-150

CAS No.: 1793080-72-4

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VX-150 (VX150)

货号: PC-22573Not For Human Use, Lab Use Only.

VX-150 is a highly selective, orally bioavailable NaV1.8 channel inhibitor, shows >400-fold selectivity over other sodium channel subtypes, induces analgesia in a variety of evoked pain tests, without affecting subject safety.

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5 mg ￥1580 In stock
10 mg ￥2480 In stock
25 mg ￥3980 In stock
50 mg ￥5880 In stock
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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

VX-150 is a highly selective, orally bioavailable NaV1.8 channel inhibitor, shows >400-fold selectivity over other sodium channel subtypes, induces analgesia in a variety of evoked pain tests, without affecting subject safety.

物理化学性质&存储条件

分子量 516.34
分子式 C21H17F4N2O7P
外观性状 Solid
CAS No.
储存条件
固体粉末
-20°C 12 个月; 4°C 6 个月
配置液
-80°C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO
Chemical Name/SMILES

(4-(2-(4-Fluoro-2-methylphenoxy)-4-(trifluoromethyl)benzamido)-2-oxopyridin-1(2H)-yl)methyl dihydrogen phosphate

参考文献

1. Hijma HJ, et al. Pain Med. 2021 Aug 6;22(8):1814-1826.

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