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首页-小分子抑制剂&激动剂-Membrane Transporter/Ion Channel-Sodium Channel-PF-04856264
PF-04856264

Chemical Structure : PF-04856264

CAS No.: 1235397-05-3

PF-04856264 (PF04856264)

货号: PC-61853Not For Human Use, Lab Use Only.

PF-04856264 is a potent, selective Nav1.7 blocker with IC50 of 28 nM, dispalys >1,000-fold selectivity over Nav1.5.

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5 mg ¥1280 In stock
10 mg ¥1980 In stock
25 mg ¥3280 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

PF-04856264 is a potent, selective Nav1.7 blocker with IC50 of 28 nM, dispalys >1,000-fold selectivity over Nav1.5.
PF-04856264 state-dependently and selectively inhibits Nav1.7 and significantly reduces OD1-induced spontaneous pain when delivered locally and systemically.

物理化学性质&存储条件

分子量 437.5
分子式 C20H15N5O3S2
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

3-cyano-4-(2-(1-methyl-1H-pyrazol-5-yl)phenoxy)-N-(thiazol-2-yl)benzenesulfonamide

参考文献

1. McCormack K, et al. Proc Natl Acad Sci U S A. 2013 Jul 16;110(29):E2724-32.

2. Deuis JR, et al. Toxins (Basel). 2016 Mar 17;8(3). pii: E78.

3. Deuis JR, et al. Sci Rep. 2017 Jan 20;7:40883.

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