MC-1-F2 is a FOXC2 inhibitor. MC-1-F2 shows a binding affinity (Kd) of 26 µM for full-length FOXC2. MC-1-F2 reduces epithelial-mesenchymal transition (EMT) markers in breast cancer cells, suppresses cancer stem cell (CSC) properties and reduces invasiveness in castration-resistant prostate cancer (CRPC) cells. MC-1-F2 can be used for the study of CRPC and breast cancer[1][2].
Molecular Weight:
746.87
Purity:
99.78
CAS Number:
[2376894-10-7]
Formula:
C37H46N16O2
Target:
Cadherin,c-Myc
Application Notes:
MCE Product type: Reference compound1
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