|M28266||KL-11743||KL-11743 is a potent, orally active, and glucose-competitive inhibitor of the class I glucose transporters, with IC50s of 115, 137, 90, and 68 nM for GLUT1, GLUT2, GLUT3, and GLUT4, respectively. KL-11743 specifically blocks glucose metabolism. KL-11743 can synergize with electron transport inhibitors to induce cell death.|
|M8661||BAY-588||BAY-588 is an inactive control probe for BAY-876.|
|M7744||Dihydrokainic acid||Dihydrokainic acid is a selective inhibitor of the GLT-1 glutamate transporter.|
|M6316||1,9-Dideoxyforskolin||1,9-Dideoxyforskolin is a inactive analog of forskolin|
|M6156||WZB117||WZB117 is an inhibitor of Glucose Transporter 1 (GLUT1). It inhibited cell proliferation in lung cancer A549 cells and breast cancer MCF7 cells with an IC50 of approximately 10 μM.|
|M4970||STF-31||STF-31 is a selective glucose transporter GLUT1 inhibitor, with an IC50 of 1 μM. STF-31 is also a NAMPT inhibitor.|
|M20762||DRB18||DRB18 is a pan-GLUT (glucose transporters) inhibitor that inhibits growth and proliferation in several different cancer types with IC50 high nM range.|
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