CAS 2055918-71-1

Formel: C26H22F2N6O4S

InChl: InChI=1S/C26H22F2N6O4S/c1-13-7-15-9-21(32-20(15)10-19(13)33-39(3,36)37)24(35)16-11-31-34(26(16)29)22-12-30-23(8-14(22)2)38-25-17(27)5-4-6-18(25)28/h4-12,32-33H,29H2,1-3H3

InChI Key: YVXUHNOWRKWXSJ-UHFFFAOYSA-N

SMILES: CC1=CC2=C(C=C1NS(=O)(=O)C)NC(=C2)C(=O)C3=C(N(N=C3)C4=CN=C(C=C4C)OC5=C(C=CC=C5F)F)N

CH6953755

CAS: 2055918-71-1

CH6953755

Formel: C₂₆H₂₂F₂N₆O₄S

Reinheit: 98.5%

Molekulargewicht: 552.55

Ref: 54-BUP07059

CH6953755

CAS: 2055918-71-1

Formel: C₂₆H₂₂F₂N₆O₄S

Reinheit: 98%

Molekulargewicht: 552.5525

Ref: IN-DA01MVST

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

Formel: C₂₆H₂₂F₂N₆O₄S

Reinheit: 98.87%

Farbe und Form: Solid

Molekulargewicht: 552.552

Ref: TM-T10784

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