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BAY-876, MedChemExpress
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Quantity:
2 mg
5 mg
10 mg
50 mg
100 mg
Unit Size:
100mg
10mg
2mg
50mg
5mg
Description
BAY-876 is an orally active and selective glucose transporter 1 (GLUT1) inhibitor with an IC50 of 2 nM. BAY-876 is >130-fold more selective for GLUT1 than GLUT2, GLUT3, and GLUT4. BAY-876 is also a potent blocker of glycolytic metabolism and ovarian cancer growth.
Specifications
Specifications
| Chemical Name or Material | BAY-876 |
| CAS | 1799753-84-6 |
| Color | White |
| Purity Grade Notes | Research |
| Molecular Formula | C24H16F4N6O2 |
| Quantity | 5 mg |
| Solubility Information | DMSO : ≥ 100 mg/mL (201.44 mM) ∣Methanol : 1 mg/mL (2.01 mM; ultrasonic and warming and heat to 60°C) |
| SMILES | O=C(C1=NC2=CC(F)=CC=C2C(C(NC3=C(C)N(CC4=CC=C(C#N)C=C4)N=C3C(F)(F)F)=O)=C1)N |
| Molecular Weight (g/mol) | 496.42 |
| Formula Weight | 496.42 |
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Research purposes only
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