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1202758-21-1

1202758-21-1 Structure

1202758-21-1 Structure
IdentificationBack Directory
[Name]

CNX-500
[CAS]

1202758-21-1
[Synonyms]

CNX-500
N1-(3-(3-((4-((3-acrylamidophenyl)amino)-5-methylpyrimidin-2-yl)amino)phenoxy)propyl)-N5-(15-oxo-19-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)-4,7,10-trioxa-14-azanonadecyl)glutaramide
Pentanediamide, N1-[19-[(3aS,4S,6aR)-hexahydro-2-oxo-1H-thieno[3,4-d]imidazol-4-yl]-15-oxo-4,7,10-trioxa-14-azanonadec-1-yl]-N5-[3-[3-[[5-methyl-4-[[3-[(1-oxo-2-propen-1-yl)amino]phenyl]amino]-2-pyrimidinyl]amino]phenoxy]propyl]-
[Molecular Formula]

C48H68N10O9S
[MDL Number]

MFCD30533366
[MOL File]

1202758-21-1.mol
[Molecular Weight]

961.18
Chemical PropertiesBack Directory
[density ]

1.232±0.06 g/cm3(Predicted)
[form ]

Solid
[pka]

13.27±0.70(Predicted)
[color ]

White to yellow
Hazard InformationBack Directory
[Uses]

CNX-500 is a probe consisting of a covalent Btk inhibitor (CC-292) chemically linked to biotin. CNX-500 retains inhibitory activity against Btk (IC50 of 0.5 nM) and the ability to form a covalent bond with Btk. CNX-500 has low inhibitory effects on kinase epidermal growth factor receptor, and upstream Src-family kinases including Syk and Lyn[1].
[References]

[1] Evans EK, et al. Inhibition of Btk with CC-292 provides early pharmacodynamic assessment of activity in mice and humans. J Pharmacol Exp Ther. 2013 Aug;346(2):219-28. DOI:10.1124/jpet.113.203489
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