BRAFV600E/ABL2-IN-2 is a dual BRAFV600E and ABL2 kinase inhibitor, with an IC50 of 0.088 µM against human BRAFV600E and an IC50 of 0.3 µM against human ABL2. BRAFV600E/ABL2-IN-2 reduces the phosphorylation levels of downstream ERK1/2 and CrkL in melanoma cells. BRAFV600E/ABL2-IN-2 decreases the expression of P-glycoprotein (P-glycoprotein) in melanoma cells. BRAFV600E/ABL2-IN-2 induces G1 cell cycle arrest and apoptosis (Apoptosis) in melanoma cells. BRAFV600E/ABL2-IN-2 is applicable to relevant research on melanoma[1].
Molekulargewicht:
559.86
Formel:
C24H20BrClN4O3S
Target-Kategorie:
Apoptosis,PERK,P-glycoprotein
Anwendungsbeschreibung:
MCE Product type: Reference compound
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