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Product introduction
Information DT2216 DT2216 is a potent and selective degrader of BCL-XL based on PROTAC technology. DT2216 inhibits various BCL-XL-dependent leukemia and cancer cells but considerably less toxic to platelets. Targets BCL-XL In vitro DT2216 is a BCL-XL proteolysis targeting chimera (PROTAC) that targets BCL-XL to the Von Hippel-Lindau (VHL) E3 ligase for degradation. DT2216 is more potent against various BCL-XL-dependent leukemia and cancer cells but significantly less toxic to platelets than ABT263 in vitro because VHL is poorly expressed in platelets. In vivo DT2216 effectively inhibits the growth of several xenograft tumors as a single agent or in combination with other chemotherapeutic agents, without causing significant thrombocytopenia. Cell Research(from reference) Cell lines:MOLT-4, RS4;11, NCI-H146, MDA-MB-231, PC-3, HepG2, SW620, 786-O, WI-38, HEK 293T cells Concentrations:0.1 μM, 0.3 μM Incubation Time:24 h
Chinese name
DT2216
English name
DT2216
Chinese alias
-
English alias
(2S,4R)-1-((S)-2-(7-(4-((R)-3-(4-(N-(4-(4-((2-(4-chlorophenyl)-5,5-dimethylcyclohex-1-enyl)methyl)piperazin-1-yl)benzoyl)sulfamoyl)-2-(trifluoromethylsulfonyl)phenylamino)-4-(phenylthio)butyl)piperazin-1-yl)-7-oxoheptanamido)-3,3-dimethylbutanoyl)-4-hydro
CAS number
2365172-42-3
molecular formula
C77H96ClF3N10O10S4
molecular weight
1542.36 g/mol
Exact mass
-
PSA
321.000 Ų
Logp
12.800
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DT2216 100mg

DT2216 100mg; supplied for laboratory research, analysis, inspection, and scientific procurement use; specifications: 100mg; ≥98%.

item number:D414272-100mg
Product model:100mg
level: 100mg; ≥98%
Lead Time:30days
sold 702 Items
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100mg

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