GLUT Glucose transporter

Cat.No.	Name	Information
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.