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首页-小分子抑制剂&激动剂-Membrane Transporter/Ion Channel-P2X Receptor-NP-1815-PX
NP-1815-PX

Chemical Structure : NP-1815-PX

CAS No.: 1239578-79-0

NP-1815-PX (P2X4 antagonist)

货号: PC-22525Not For Human Use, Lab Use Only.

NP-1815-PX is a potent, selective P2X4 receptor (P2X4R) antagonist, inhibits P2X4R-mediated [Ca2+]i increase in hP2X4R-1321N1 cells with IC50 of 0.26  μM.

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纯度 & COA & 质检文件 纯度: >98% (HPLC)

生物&药学活性

NP-1815-PX is a potent, selective P2X4 receptor (P2X4R) antagonist, inhibits P2X4R-mediated [Ca2+]i increase in hP2X4R-1321N1 cells with IC50 of 0.26  μM.
NP-1815-PX has no effect on ATP-induced [Ca2+]i increase in hP2X7R- and rP2X3R-1321N1 cells, with IC50 of >30 μM for hP2X1R, rat (r) P2X3R, hP2X2/3R and hP2X7R, and 7.3 μM for hP2X2R.
NP-1815-PX inhibits ATP-mediated responses in primary cultured microglial cells.
NP-1815-PX (10 and 30 pmol/mouse) exhibits an inhibitory effect on mechanical allodynia in a model of herpetic pain.

物理化学性质&存储条件

分子量 402.43
分子式 C21H14N4O3S
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

5-[3-(5-thioxo-4H-[1,2,4]oxadiazol-3-yl)phenyl]-1H-naphtho[1, 2-b][1,4]diazepine-2,4(3H,5H)-dione

参考文献

1. Matsumura Y, et al. Sci Rep. 2016 Aug 31;6:32461.

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