GSK-1482160 is an orally active and blood-brain barrier penetrant P2X7 receptor (P2X7R) negative allosteric modulator with pIC50s of 8.5 (human) and 6.5 (rat). GSK-1482160 reduces the efficacy of ATP at the P2X7 receptor without affecting its affinity, thereby inhibiting the release of IL-1beta. GSK-1482160 is an effective radioligand and can be labeled with radioactive isotopes like 11C or 18F to image P2X7R. GSK-1482160 can be used for the studies of chronic joint pain and chronic constriction injury (CCI)[1][2][3].
Molekulargewicht:
334.72
Reinheit:
98.67
CAS Nummer:
[1001389-72-5]
Formel:
C14H14ClF3N2O2
Target-Kategorie:
Interleukin Related,P2X Receptor
Anwendungsbeschreibung:
MCE Product type: Reference compound
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