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首页-小分子抑制剂&激动剂-Membrane Transporter/Ion Channel-Sodium Channel-A-803467
A-803467

Chemical Structure : A-803467

CAS No.: 944261-79-4

A-803467 (A 803467, A803467)

货号: PC-42804Not For Human Use, Lab Use Only.

A-803467 (A803467) potent and selective Nav1.8 sodium channel blocker with IC50 of 8 nM.

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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

A-803467 (A803467) is a potent and selective Nav1.8 sodium channel blocker with IC50 of 8 nM.
A-803467 displays >100-fold selectivity versus human Nav1.2, Nav1.3, Nav1.5, and Nav1.7 (IC50s>1 uM).
A-803467 potently blocks tetrodotoxin-resistant currents (IC50= 140 nM) and the generation of spontaneous and electrically evoked action potentials in vitro in rat dorsal root ganglion neurons.
A-803467 attenuates neuropathic and inflammatory pain in the rat.

物理化学性质&存储条件

分子量 357.7876
分子式 C19H16ClNO4
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

2-Furancarboxamide, 5-(4-chlorophenyl)-N-(3,5-dimethoxyphenyl)-

参考文献

1. Jarvis MF, et al. Proc Natl Acad Sci U S A. 2007 May 15;104(20):8520-5.

2. McGaraughty S, et al. J Pharmacol Exp Ther. 2008 Mar;324(3):1204-11.

3. Joshi SK, et al. J Pain. 2009 Mar;10(3):306-15.

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