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ChemicalBook--->CAS DataBase List--->2166387-64-8

2166387-64-8

2166387-64-8 Structure

2166387-64-8 Structure
IdentificationBack Directory
[Name]

BI-3812
[CAS]

2166387-64-8
[Synonyms]

BI-3812
CPD1815
BI3812;BI 3812
1-(5-Chloro-4-((8-methoxy-1-methyl-3-(2-(methylamino)-2-oxoethoxy)-2-oxo-1,2-dihydroquinolin-6-yl)amino)pyrimidin-2-yl)-N,N-dimethylpiperidine-4-carboxamide
4-Piperidinecarboxamide, 1-[5-chloro-4-[[1,2-dihydro-8-methoxy-1-methyl-3-[2-(methylamino)-2-oxoethoxy]-2-oxo-6-quinolinyl]amino]-2-pyrimidinyl]-N,N-dimethyl-
[Molecular Formula]

C26H32ClN7O5
[MDL Number]

MFCD31657385
[MOL File]

2166387-64-8.mol
[Molecular Weight]

558.03
Chemical PropertiesBack Directory
[density ]

1.40±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO:22.92(Max Conc. mg/mL);41.07(Max Conc. mM)
[form ]

Solid
[pka]

14.73±0.46(Predicted)
[color ]

Off-white to pink
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Uses]

BI-3812 is a highly efficient BCL6 inhibitor that is capable of suppressing the BTB domain of BCL6, with an IC50 value of ≤ 3 nM, exhibiting antitumor activity[1].
[Biological Activity]

BI-3812 is a potent BCL6 inhibitor with IC50 less than 3 nM.
[in vivo]

BI-3812 is a BCL6 inhibitor, with an IC 50 of ≤3 nM. BI-3812 shows an IC 50 of 40 nM for the cellular BCL6.

[target]

TargetValue
BCL6
(Cell-free assay)
3 nM
[References]

[1] Kerres N, et al. Chemically Induced Degradation of the Oncogenic Transcription Factor BCL6. Cell Rep. 2017 Sep 19;20(12):2860-2875. DOI:10.1016/j.celrep.2017.08.081
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