CAS 1799753-84-6

2,4-Quinolinedicarboxamide, N4-[1-[(4-cyanophenyl)methyl]-5-methyl-3-(trifluoromethyl)-1H-pyrazol-4-yl]-7-fluoro-

CAS: 1799753-84-6

Fórmula: C₂₄H₁₆F₄N₆O₂

Pureza: 98%

Forma y color: Solid

Peso molecular: 496.4165

Ref: IN-DA0021JG

N4-[1-[(4-Cyanophenyl)Methyl]-5-Methyl-3-(Trifluoromethyl)-1H-Pyrazol-4-yl]-7-Fluoro-2,4-Quinolinedicarboxamide

CAS: 1799753-84-6

N4-[1-[(4-Cyanophenyl)Methyl]-5-Methyl-3-(Trifluoromethyl)-1H-Pyrazol-4-yl]-7-Fluoro-2,4-Quinolinedicarboxamide

Pureza: 98%

Peso molecular: 496.42g/mol

Ref: 54-PC108561

BAY-876

CAS: 1799753-84-6

BAY-876

Pureza: ≥95%

Peso molecular: 496.42g/mol

Ref: 54-BUP07439

BAY-876

CAS: 1799753-84-6

BAY-876 is a selective and orally GLUT1 inhibitor. BAY-876 inhibits glycolytic metabolism and exhibits antitumor activity. Cost-effective and quality-assured.

Fórmula: C₂₄H₁₆F₄N₆O₂

Pureza: 98.61% - 99.78%

Forma y color: Solid

Peso molecular: 496.42

Ref: TM-T3713

BAY-876

Producto controlado

CAS: 1799753-84-6

Applications BAY-876 is a potent glucose transporter 1 (GLUT 1) selective small molecular inhibitor that showed good metabolic stability in vitro and high oral bioavailability in vivo.
References Siebeneicher, H., et al.: ChemMedChem, 11, 2261 (2016)

Fórmula: C₂₄H₁₆F₄N₆O₂

Forma y color: Light Yellow To Beige

Peso molecular: 496.42

Ref: TR-B127530

BAY 876

CAS: 1799753-84-6

Selective and potent inhibitor of glucose transporter GLUT1 with IC50 of 2 nM. The compound limits glucose uptake and is able to block basal as well as stress-regulated glycolysis in ovarian cancer cells. It supresses proliferation, viability and tumorigenicity of ovarian cancer cells.

Fórmula: C₂₄H₁₆F₄N₆O₂

Pureza: Min. 95%

Forma y color: Solid

Peso molecular: 496.42 g/mol

Ref: 3D-BB166031