CAS 2055918-71-1

CH6953755

CAS: 2055918-71-1

Formel: C₂₆H₂₂F₂N₆O₄S

Reinheit: 98%

Molekulargewicht: 552.5525

Ref: IN-DA01MVST

CH6953755

CAS: 2055918-71-1

CH6953755

Formel: C₂₆H₂₂F₂N₆O₄S

Reinheit: ≥98%

Molekulargewicht: 552.55

Ref: 54-BUP07059

CH6953755

CAS: 2055918-71-1

N-(2-(5-Amino-1-(6-(2,6-difluorophenoxy)-4-methylpyridin-3-yl)-1H-pyrazole-4-carbonyl)-5-methyl-1H-indol-6-yl)methanesulfonamide

Formel: C₂₆H₂₂F₂N₆O₄S

Reinheit: 98%

Molekulargewicht: 552.55

Ref: IN-DG01239518

CH6953755

CAS: 2055918-71-1

CH6953755 is a potent and selective inhibitor of the protein interactions between the N-terminal domain of the human erythrocyte membrane protein band 3 (HEMB) and erythrocyte membrane protein band 4.1 (EMAP). It is also an activator of ligand binding to the receptor. CH6953755 has been shown to inhibit ion channels in a variety of cell types, including neuronal cells and myocytes, leading to reduced excitability. This compound has a high purity level as it is not metabolized by enzymes.

Formel: C₂₆H₂₂F₂N₆O₄S

Reinheit: Min. 95%

Molekulargewicht: 552.6 g/mol

Ref: 3D-FHD91871

CH6953755

CAS: 2055918-71-1

CH6953755: oral YES1 kinase inhibitor, IC50 1.8 nM, potent, selective, anticancer, halts cell proliferation.

Formel: C₂₆H₂₂F₂N₆O₄S

Reinheit: 98.87%

Farbe und Form: Solid

Molekulargewicht: 552.55

Ref: TM-T10784