A-317491 sodium salt hydrate

A-317491 钠盐水合物

A-317491 sodium salt hydrate

A659417-5mg

5mg

≥99%

2-8°C储存,干燥

冰袋运输

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

C33H29NNaO9

606.57 g/mol

O=C(C1=CC(C(N(CC2=CC=CC(OC3=CC=CC=C3)=C2)[C@H]4CCCC5=C4C=CC=C5)=O)=C(C(O)=O)C=C1C(O)=O)O.[Na].O

H2O : 100 mg/mL (164.86 mM; Need ultrasonic)