A-317491 sodium salt hydrate is a potent, selective and non-nucleotide antagonist of P2X 3 and P2X 2/3 receptors , with K i s of 22, 22, 9, and 92 nM for hP2X 3 , rP2X 3 , hP2X 2/3 , and rP2X 2/3 , respectively. A-317491 sodium salt hydrate is highly sele Appearance:Solid IC50& Target:P2X3 Receptor In Vitro:A-317491 potently blocks recombinant human and rat P2X 3 and P2X 2/3 receptor-mediated calcium flux (K i =22-92 nM). A-317491 (1 nM-10 μM) produces a concentration-dependent block of dorsal root ganglion (DRG) currents with an IC 50 of 15 nM. MC In Vivo:A-317491 (0.1-30mg/kg; a single s.c.) dose-dependently reverses inflammatory mechanical hyperalgesia in rats. A-317491 (3-30mg/kg; a single .v.) exhibits the plasma half-life (7.38 h), clearance rate (1.83 L/h/kg), and volume of distribution (0.17 Biological Activity:A-317491 sodium salt hydrate is a potent, selective and non-nucleotide antagonist of P2X 3 and P2X 2/3 receptors , with K i s of 22, 22, 9, and 92 nM for hP2X 3 , rP2X 3 , hP2X 2/3 , and rP2X 2/3 , respectively. A-317491 sodium salt hydrate is highly sele
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A-317491 sodium salt hydrate
CAS number：unknown molecular formula：C33H29NNaO9
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| Chinese alias | A-317491 钠盐水合物 | ||
| English alias | - | ||
| CAS number | unknown | molecular formula | C33H29NNaO9 |
| molecular weight | 606.57 g/mol | Exact mass | ≥99% |
| PSA | - | logp | - |
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