MC-1-F2

MC-1-F2
  • CAS No.:2376894-10-7
  • Grade:99.69%
  • Formula:C37H46N16O2
  • M.W.:746.87
  • Solvent:≥ 2.5 mg/mL (3.35 mM); Clear solution

Overview

MC-1-F2 is a FOXC2 inhibitor. MC-1-F2 shows a binding affinity ( K d ) 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 .

Application

Products | Products > Disease Areas > Cancer | Products > Disease Areas > Breast Cancer | Products > Signaling Pathways > Metabolic Enzyme/Protease | Products > Signaling Pathways > Apoptosis | Products > Signaling Pathways > Cytoskeleton | Products > Research Areas > Cancer | Products > Research Areas > Cancer > Cancer Targeted Therapy | Products > Research Areas > Cancer > Cancer Stem Cells | Products > Research Areas > Cancer > Cancer Drug Resistance | Products > Research Areas > Cancer > Cancer Metabolism and Metastasis | Products > Signaling Pathways > FOXC | Products > Signaling Pathways > c-Myc | Products > Signaling Pathways > Cadherin

Product Information

  • Catalog No.: HY-149894
  • CAS No.: 2376894-10-7
  • Molecular Formula: C37H46N16O2
  • Molecular Weight: 746.87
  • Purity: 99.69%
  • Storage: 4°C, stored under nitrogen * In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen)
  • Solubility: ≥ 2.5 mg/mL (3.35 mM); Clear solution
  • Availability: In-stock

Source

Original product source


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