| References: |
STF-31 is an inhibitor of GLUT1 (IC50 = ~1 µM) that blocks glucose uptake.It induces necrosis in cancer cells that lack the von Hippel-Lindau tumor suppressor gene, which overexpress GLUT1.Although STF-31 binds GLUT1, suggesting a direct effect, STF-31 also inhibits nicotinamide phosphoribosyltransferase, an enzyme that induces GLUT1 expression. STF-31 is also toxic to human pluripotent stem cells (hPSCs) and can be used to selectively eliminate hPSCs from mixed cultures. For the detailed information of STF-31, the solubility of STF-31 in water, the solubility of STF-31 in DMSO, the solubility of STF-31 in PBS buffer, the animal experiment (test) of STF-31, the cell expriment (test) of STF-31, the in vivo, in vitro and clinical trial test of STF-31, the EC50, IC50,and affinity,of STF-31, For the detailed information of STF-31, the solubility of STF-31 in water, the solubility of STF-31 in DMSO, the solubility of STF-31 in PBS buffer, the animal experiment (test) of STF-31, the cell expriment (test) of STF-31, the in vivo, in vitro and clinical trial test of STF-31, the EC50, IC50,and affinity,of STF-31, Please contact DC Chemicals. |
