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. |
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