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A P2X7 receptor antagonist, inhibits ATP-induced dye uptake in HEK293 cells expressing human purinergic P2X7 receptors (IC50 = 22.4 nM), inhibits common lancehead (B. atrox) venom proteolysis in a concentration-dependent manner, inhibits ATP-induced IL-1ß secretion in human THP-1 monocytes and primary mouse peritoneal macrophages (IC50s = 9.8 and 11.2 nM, respectively), inhibits common lancehead (B. atrox) and jararaca (B. jararaca) venom-induced skin hemorrhage in mice when intradermally administered at 3 mg/kg, inhibits carrageenan-induced paw edema in mice at 0.01 to 1 mg/kg. Formulation: A solid. InChI: InChI=1S/C16H10O3/c17-14-11-8-4-5-9-12(11)15(18)16(19)13(14)10-6-2-1-3-7-10/h1-9,19H. InChIKey: KUKDVSFMDRAXML-UHFFFAOYSA-N. SMILES: O=C1C(O)=C(C(C2=C1C=CC=C2)=O)C3=CC=CC=C3
This website uses cookies, which are necessary for the technical operation of the website and are always set. Other cookies, which increase the usability of this website, serve for direct advertising or simplify interaction with other websites and social networks, will only be used with your consent.
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