CT-721 is a potent and time-dependent Bcr-Abl kinase inhibitor with an IC50 of 21.3 nM for wild-type Bcr-Abl kinase, and possesses anti-chronic myeloid leukemia (CML) activities[1]. CT-721 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
Molekulargewicht:
525.04
CAS Nummer:
[1388710-60-8]
Formel:
C30H29ClN6O
Target-Kategorie:
Bcr-Abl
Anwendungsbeschreibung:
MCE Product type: Reference compound
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