P2X Receptor

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Catalog No.
Product Name
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  1. P2X7 receptor antagonist

    A 740003 is a novel competitive antagonist of P2X7 receptors (IC50 values = 40 nM for human and 18 nM for rat).
  2. P2X1 antagonist

    NF279 is a suramin analog that acts as a highly selective, competitive, and reversible ATP-antagonist of P2X receptor (IC50/KB ~ 1 μM in smooth muscle).
  3. P2X3 and P2X2/3 receptor antagonist

    A-317491 sodium salt hydrate is a non-nucleotide P2X3 and P2X2/3 receptor antagonist, which inhibits calcium flux mediated by the receptors.
  4. P2X7 receptor antagonist

    A-438079 HCl is a competitive P2X7 receptor antagonist (pIC50 = 6.9 for the inhibition of Ca2+ influx in the human recombinant P2X7 cell line). Devoid of activity at other P2 receptors (IC50 >> 10 uM).
  5. P2X3/P2X2/3 receptor antagonist

    AF-353 is a novel, potent and orally bioavailable P2X3/P2X2/3 receptor antagonist, inhibits human and rat P2X3 (pIC50= 8.0).
  6. P2X7 receptor antagonist

    A 438079 Hcl is a competitive P2X7 receptor antagonist (pIC50 = 6.9 for the inhibition of Ca2+ influx in the human recombinant P2X7 cell line).
  7. P2X7 receptor antagonist

    A-804598 is a P2X7 selective, competitive antagonist with the IC50s value for human, rat and mouse channels of 11, 10 and 9 nM, respectively.
  8. P2X7 receptor antagonist

    JNJ-54175446 is a potent and selective brain penetrant P2X7 receptor antagonist, with pIC50s of 8.46 and 8.81 for hP2X7 receptor and rP2X7 receptor, respectively.
  9. P2X3R antagonist

    Gefapixant is an orally active P2X3 receptor (P2X3R) antagonist with IC50s of ~30 nM versus recombinant hP2X3 homotrimers and 100-250 nM at hP2X2/3 heterotrimeric receptors.
  10. P2X4 antagonist

    PSB-12062 is a potent and selective P2X4 antagonist with an IC50 of 1.38 μM for human P2X4.
  11. P2X7R antagonist

    AZ10606120 dihydrochloride is a selective, high affinity antagonist for P2X7 receptor (P2X7R) at human and rat with an IC50 of ~10?nM.
  12. P2X7 selective antagonist

    A 839977 is a P2X7 selective antagonist.
  13. P2X7 receptor antagonist

    CE-224535 is a selective P2X7 receptor antagonist.
  14. purinergic P2X2/3 receptors antagonist

    Minodronic acid (YM-529) is an antagonist of purinergic P2X2/3 receptors involved in pain.

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