A novel, potent, orally bioavailable antagonist of P2X3/P2X2/3 receptors (pIC50 = 8 in human and rat, pIC50 = 7.3 for human P2X2/3 receptor). Shown to be highly brain penetrant with a brain to plasma ratio of 6. Blocks agonist-evoked intracellular Ca2+ f
Reinheit:
99% (HPLC)
Formulierung:
Supplied as a light brown powder.
CAS Nummer:
[927887-18-1]
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