GLUT
Inhibitory Selectivity
Isoform-specific Inhibitors
GLUT Products
| Catalog No. | Information | Product Use Citations | Product Validations |
|---|---|---|---|
| S7931 |
STF-31STF-31 is a selective glucose transporter GLUT1 inhibitor. |
NP69 cells were transfected with LMP1 expression plasmid and treated with STF-31 or infected with lentivirus expressing shGlut-1 for 48 h. The cells were then lysed and subjected to Western blotting using specific antibodies against Glut-1 and cleaved caspase 3. β-Actin expression was used as the loading control.
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| S7927 |
WZB117WZB117 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. |
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| S8452 |
BAY-876BAY-876 is a potent and selective GLUT1 inhibitor (IC50=0.002 μM) with a selectivity factor of >100 against GLUT2, GLUT3, and GLUT4. |
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| S9636 |
DRB18DRB18 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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| S5748 |
4′-Deoxyphlorizin4'-Deoxyphlorizin is an inhibitor of the glucose transport system. |
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| S0235 |
Lavendustin BLavendustin B inhibits HIV-1 integrase (IN) interaction with its cognate cellular cofactor lens epithelium-derived growth factor (LEDGF/p75). Lavendustin B is an inhibitor of Tyrosine Kinase and also a competitive inhibitor of glucose transporter 1 (Glut1). |
| Catalog No. | Information | Product Use Citations | Product Validations |
|---|---|---|---|
| S7931 |
STF-31STF-31 is a selective glucose transporter GLUT1 inhibitor. |
NP69 cells were transfected with LMP1 expression plasmid and treated with STF-31 or infected with lentivirus expressing shGlut-1 for 48 h. The cells were then lysed and subjected to Western blotting using specific antibodies against Glut-1 and cleaved caspase 3. β-Actin expression was used as the loading control.
|
|
| S7927 |
WZB117WZB117 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. |
||
| S8452 |
BAY-876BAY-876 is a potent and selective GLUT1 inhibitor (IC50=0.002 μM) with a selectivity factor of >100 against GLUT2, GLUT3, and GLUT4. |
||
| S9636 |
DRB18DRB18 is a pan-GLUT (glucose transporters) inhibitor that inhibits growth and proliferation in several different cancer types with IC50 high nM range. |
||
| S5748 |
4′-Deoxyphlorizin4'-Deoxyphlorizin is an inhibitor of the glucose transport system. |
||
| S0235 |
Lavendustin BLavendustin B inhibits HIV-1 integrase (IN) interaction with its cognate cellular cofactor lens epithelium-derived growth factor (LEDGF/p75). Lavendustin B is an inhibitor of Tyrosine Kinase and also a competitive inhibitor of glucose transporter 1 (Glut1). |
