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| Product | Description | |
|---|---|---|
| STF-31 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| STF-31 | STF-31 is a selective glucose transporter GLUT1 inhibitor. It effectively eliminates undifferentiated human pluripotent stem cells (hPSCs) from culture. Synonyms: STF 31; 4-[[(4-tert-butylphenyl)sulfonylamino]methyl]-N-pyridin-3-ylbenzamide. Grades: >98%. CAS No. 724741-75-7. Molecular formula: C23H25N3O3S. Mole weight: 423.53. |  |
| STF-31 | STF-31 is a selective inhibitor of glucose transporter 1 (GLUT1), with an IC50 of 1 ?M. STF-31 is also a NAMPT inhibitor. STF-31 inhibits glucose uptake in renal cell carcinoma (RCC) 4 cells[1][2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 724741-75-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-18728. |  |
| Glucose Transporter Inhibitor III (STF-31) | A cell-permeable sulfonamide that selectively inhibits the growth of VHL-deficient renal cell carcinomas (RCCs) dose-dependently (0-5uM) by directly targeting glucose transporter 1 (GLUT1), which is up-regulated by HIF (hypoxia-inducible factor) transcription factor in VHL-deficient cells. It elicits decreased oxidative phosphorylation associated with aerobic glycolysis and leads to necrosis, which is consistent with the effect induced by GLUT1 RNA interference. It does not bind to other glucose transporters, and does not inhibit a broad range of 50 tested kinases. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. |  Worldwide |
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