CAS 2301916-69-6

(2S,4R)-1-((S)-3,3-Dimethyl-2-(3-(2-(4-((4-((3-(N-methylmethylsulfonamido)benzyl)amino)-5-(trifluoromethyl)pyrimidin-2-yl)amino)phenoxy)ethoxy)propanamido)butanoyl)-4-hydroxy-N-(4-(4-methylthiazol-5-y

CAS : 2301916-69-6

(2S,4R)-1-((S)-3,3-Dimethyl-2-(3-(2-(4-((4-((3-(N-methylmethylsulfonamido)benzyl)amino)-5-(trifluoromethyl)pyrimidin-2-yl)amino)phenoxy)ethoxy)propanamido)butanoyl)-4-hydroxy-N-(4-(4-methylthiazol-5-y

Degré de pureté : 99%

Masse moléculaire : 996.15g/mol

Ref: 54-PC1007891

PROTAC FAK degrader 1

CAS : 2301916-69-6

PROTAC FAK degrader 1 is a selective and potent degrader of focal adhesion kinase (Fak) (IC50 of 6.5 nM).

Formule : C₄₇H₅₆F₃N₉O₈S₂

Degré de pureté : 98%

Couleur et forme : Solid

Masse moléculaire : 996.13

Ref: TM-T13840

Protac fak degrader 1

CAS : 2301916-69-6

Protac Fak Degrader 1 is a research tool for pharmacology and cell biology. It is used to inhibit ion channels, ligands and receptors. Protac Fak Degrader 1 has been shown to be an activator of the G protein-coupled receptor (GPCR) family. Protac Fak Degrader 1 is a peptide that binds to the extracellular domain of the receptor, which prevents it from interacting with other proteins or ligands. Protac Fak Degrader 1 is purified at high purity and can be used as a reagent in life science experiments.

Formule : C₄₇H₅₆F₃N₉O₈S₂

Degré de pureté : Min. 95%

Masse moléculaire : 996.1 g/mol

Ref: 3D-BSD91669