JB170 is a potent and highly specific PROTAC-mediated AURORA-A (Aurora Kinase) degrader (DC50=28 nM) by linking Alisertib, to the Cereblon-binding molecule Thalidomide. JB170 preferentially binds AURORA-A (EC50=193 nM) over AURORA-B (EC50=1.4 µM). JB170-mediated S-phase arrest is caused specifically by AURORA-A depletion. JB170 has excellent ability to inhibit non-catalytic function of AURORA-A kinase[1].
Molekulargewicht:
963.36
Reinheit:
98.97
CAS Nummer:
[2705844-82-0]
Formel:
C48H44ClFN8O11
Target-Kategorie:
Aurora Kinase,PROTACs
Anwendungsbeschreibung:
MCE Product type: Reference compound
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