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

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Cat. No. Product Name Information
PC-28215

EVT-401

P2X7R antagonist

EVT-401 (EVT401) is a potent, highly selective human P2X7 receptor (P2X7R) antagonist with Ki of 7.6 nM in competitive binding assays.
PC-27099

P2X7R antagonist A20

P2X7 antagonist

P2X7R antagonist A20 (Compound 9q) is a potent, selective antagonist of ATP-gated channel P2X7 receptor (P2X7R) with IC50 of 18 nM (hP2X7), exhibits non-competitive negative allosteric mode of antagonism.
PC-26954

(Rac)-EVT-401

P2X7R antagonist

(Rac)-EVT-401 is the racemate form of EVT-401, a potent, highly selective human P2X7 receptor (P2X7R) antagonist with Ki of 7.6 nM in competitive binding assays.
PC-26569

UB-ALT-P2

P2X7 antagonist

UB-ALT-P2 is a potent and selective brain-penetrant negative allosteric modulator / antagonist of ATP-gated P2X7 receptor (P2X7R) with IC50 of 1.3 nM.
PC-26328

Funopixant

P2X3 antagonist

Funopixant is a potent, selective P2X3 receptor antagonist with IC50 of 32.45 nM for hP2X3.
PC-26167

PSB-1011

P2X2 antagonist

PSB-1011 is a potent, moderately selective rat P2X2 receptor antagonist with IC50 of 79 nM, weakly inhibits P2X1 and P2X3 receptors and shows no activity against P2X4 and P2X7 receptors.
PC-26162

PSB-15417

P2X4 antagonist

PSB-15417 is a potent, specific P2X4 receptor (P2X4R) antagonist with IC50 of 21.9 nM and 37 nM for human and rat P2X4 receptor, shows limited activity against P2X1, P2X2, P2X3 and P2X7 receptors (All IC50>2 uM).
PC-26160

MRS4719

P2X4 antagonist

MRS4719 is a potent, selective P2X4 receptor antagonist with IC50 of 0.5 uM (human P2X4R), selective versus hP2X1R, hP2X2/3R, hP2X3R.
PC-26159

PSB-0704

P2X4 antagonist

PSB-0704 is a potent, allosteric P2X4 receptor inhibitor with IC50 of 12.5 and 0.07 uM for human wt P2X4 and P2X4-E307T receptor mutant.
PC-25132

PPADS tetrasodium

P2X receptor antagonist

PPADS tetrasodiuma is a non-selective P2X receptor antagonist, inhibits recombinant P2X1, P2X12, P2X13, P2X15 with IC50 of 1-2.6 uM.
PC-22910

AZ11645373

P2X7 antagonist

AZ11645373 is a selective and potent antagonist of human P2X7 receptor, inhibits ATP-mediated release of IL-1β in LPS-stimulated THP-1 monocytes with Kb of 92 nM.
PC-22645

GSK1482160

P2X7 NAM

GSK1482160 is an orally available allosteric P2X7 receptor negative allosteric modulator (NAM) with pIC50 of 8.5 and 6.5 for human and rat P2X7R respectively.

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