P2X Receptor
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A 438079 hydrochloride
Catalog No. A14983 P2X7 receptor 拮抗剂A 438079 hydrochloride是一种竞争性P2X7受体拮抗剂(抑制人重组P2X7细胞系中Ca2+流入的pIC50 = 6.9)。 了解更多 -
JNJ-54175446
Catalog No. A18675 P2X7 receptor antagonistJNJ-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. 了解更多 -
A 839977
Catalog No. A21178 -
CE-224535
Catalog No. A21183 -
GW791343 trihydrochloride
Catalog No. A21204 P2X7 allosteric modulatorGW791343 3Hcl is a P2X7 allosteric modulator; exhibits species-specific activity and acts as a negative allosteric modulator of human P2X7 (pIC50 = 6.9 - 7.2). 了解更多 -
Minodronic acid
Catalog No. A21975 purinergic P2X2/3 receptors antagonistMinodronic acid (YM-529) is an antagonist of purinergic P2X2/3 receptors involved in pain. 了解更多 -
GW791343 HCl
Catalog No. A11107 -
Ticlopidine HCl
Catalog No. A11690 Ticlopidine是一种二磷酸腺苷(ADP)受体抑制剂。它通过阻断ADP受体来改变血小板膜的功能,从而抑制血小板聚集。这防止了糖蛋白IIb/IIIa的构象变化,从而使血小板与血纤蛋白原结合。 了解更多 -
NF 279
Catalog No. A11972 -
A-317491 sodium salt hydrate
Catalog No. A12412 P2X3 and P2X2/3 receptor 拮抗剂A-317491 sodium salt hydrate是一种非核苷酸的P2X3和P2X2/3受体拮抗剂,可抑制受体介导的钙通量。 了解更多 -
A-438079 HCl
Catalog No. A12597 P2X7 receptor 拮抗剂A-438079 HCl是一种竞争性P2X7受体拮抗剂(抑制人重组P2X7细胞系中Ca2+流入的pIC50 = 6.9)。在其他P2受体上没有活性(IC50 > 10 uM)。 了解更多