DT2216 is a potent and selective BCL-XL (Bcl-2 family member) degrader based on PROTAC technology. DT2216 causes effective degradation of BCL-XL protein by recruiting Von Hippel-Lindau (VHL) E3 ubiquitin ligase. DT2216 inhibits various BCL-XL-dependent leukemia and cancer cells but considerably less toxic to platelets. DT2216 is composed of the Bcl-2 family protein inhibitor Navitoclax-piperazine (HY-44432), a linker, and a VHL E3 ubiquitin ligase (Pink: Navitoclax-piperazine, Blue: VHL ligand, Black: linker)[1].
Molekulargewicht:
1542.36
Reinheit:
99.97
CAS Nummer:
[2365172-42-3]
Formel:
C77H96ClF3N10O10S4
Target-Kategorie:
Apoptosis,Bcl-2 Family,PROTACs
Anwendungsbeschreibung:
Reference compound
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