Branebrutinib (BMS-986195) is a highly potent, selective covalent, irreversible inhibitor of Brutons tyrosine kinase (BTK), with an IC50 of 0.1 nM[1][2]. Branebrutinib is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
Molecular Weight:
370.42
Purity:
99.78
CAS Number:
[1912445-55-6]
Formula:
C20H23FN4O2
Target:
Btk
Application Notes:
MCE Product type: Reference compound
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