A-620223 is a PARP-1 inhibitor with a Ki of 8 nM against PARP-1 and EC50 of 3 nM in a whole cell assay. A-620223 demonstrates good in vivo efficacy in a B16F10 subcutaneous murine melanoma model in combination with Temozolomide (TMZ) (HY-17364) and in an MX-1 breast xenograph model in combination with Cisplatin (HY-17394). A-620223 can be used for the studies of melanoma and breast cancer[1].
Molekulargewicht:
286.37
Reinheit:
98.84
CAS Nummer:
[272769-49-0]
Formel:
C16H22N4O
Target-Kategorie:
PARP
Anwendungsbeschreibung:
MCE Product type: Reference compound
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