Description
A PFKFB3 inhibitor (IC50 = 137 nM for human recombinant PFKFB3); inhibits PFKFB3 and glycolysis in Jurkat cells (IC50s = 1.6 and 0.847 μM, respectively); inhibits the growth of leukemia cells in vitro (IC50 = 0.33 μM for Jurkat cells); reduces tumor volume in CT-26 murine colon carcinoma syngeneic model and a BxPC-3 pancreatic cancer mouse xenograft model; enhances activity of the anti-CTLA-4 antibody in the B16/F10 mouse model of melanoma
Formal name: 1-(4-pyridinyl)-3-[7-(trifluoromethyl)-2E-quinolinyl]-2-propen-1-one
Synonyms:
Molecular weight: 328.3
CAS: 1462249-75-7
Purity: ≥95%
Formulation: A crystalline solid
Product Type|Biochemicals|Kinase Inhibitors|Carbohydrate Kinases||Product Type|Biochemicals|Small Molecule Inhibitors|Kinases||Product Type|Biochemicals|Small Molecule Inhibitors|Phosphatases||Research Area|Cancer|Cell Signaling||Research Area|Cancer|Metabolism