PARP1/c-Met-IN-2 is a highly potent, orally active, PARP1 (IC50 = 21.8 nM) and c-Met (IC50 = 30.2 nM) dual inhibitor. PARP1/c-Met-IN-2 can elevate the expression level of gammaH2AX, cause DNA damage. PARP1/c-Met-IN-2 exhibits remarkable anti-tumor efficacy in the Olaparib (HY-10162)-resistant HCT116 (HCT116OR) xenograft models. PARP1/c-Met-IN-2 can be used for the study of Colon Cancer[1].
Molekulargewicht:
676.12
Formel:
C36H30ClN7O5
Target-Kategorie:
c-Met/HGFR,DNA/RNA Synthesis,PARP
Anwendungsbeschreibung:
MCE Product type: Reference compound
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