|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.
|BAY-588 is an inactive control probe for BAY-876.
|BAY-876 is a potent, highly selective, cell-permeable inhibitor of glucose transporter GLUT1 with an IC50 of 2 nM.
|Dihydrokainic acid is a selective inhibitor of the GLT-1 glutamate transporter.
|1,9-Dideoxyforskolin is a inactive analog of forskolin
|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.
|STF-31 is a selective glucose transporter GLUT1 inhibitor, with an IC50 of 1 μM. STF-31 is also a NAMPT inhibitor.
|SLC26A3-IN-3 is a SLC26A3 inhibitor (IC50: 40 nM).
|MSNBA is a specific inhibitor of GLUT5 fructose transport in proteoliposomes.
|SLC26A3-IN-1 is an inhibitor of anion exchanger protein SLC26A3 (IC50=340 nM).
|SLC26A3-IN-2 is an orally active inhibitor of anion exchanger protein SLC26A3 (IC50=360 nM).
|MMV009085 is a potent PfHT1 (Plasmodium falciparum hexose transporter)-specific inhibitor and a potential anti-malarial agent .
|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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