ChemicalBook--->CAS DataBase List--->2056261-41-5

2056261-41-5

2056261-41-5 Structure

2056261-41-5 Structure
IdentificationBack Directory
[Name]

BRD0705
[CAS]

2056261-41-5
[Synonyms]

BRD0705
BRD0705 (BRD-0705
[Molecular Formula]

C20H23N3O
[MDL Number]

MFCD31726167
[MOL File]

2056261-41-5.mol
[Molecular Weight]

321.42
Chemical PropertiesBack Directory
[Boiling point ]

512.0±50.0 °C(Predicted)
[density ]

1.22±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO: 300 mg/mL (933.36 mM)
[form ]

Solid
[pka]

14.82±0.60(Predicted)
[color ]

White to light yellow
Hazard InformationBack Directory
[Description]

BRD0705 is a potent, paralog selective and orally active GSK3α inhibitor. BRD0705 can be used for acute myeloid leukemia.
[Uses]

BRD0705 is a potent, paralog selective and orally active GSK3α inhibitor with an IC50 of 66 nM and a Kd of 4.8 μM. BRD0705 displays increased selectivity for GSK3α (8-fold) versus GSK3β (IC50 of 515 nM). BRD0705 can be used for acute myeloid leukemia (AML) research[1].
[in vivo]

BRD0705 (30 mg/kg; oral gavage; twice daily; NSG mice) treatment impairs leukemia initiation and prolongs survival in AML mouse models[1].

Animal Model:8-week-old male NSG mice injected with MLL-AF9 AML cells[1]
Dosage:30 mg/kg
Administration:Oral gavage; twice daily
Result:Mice survival was significantly improved.
[IC 50]

GSK3α: 66 nM (IC50); GSK3α: 4.8 μM (Kd); GSK-3β(WT): 515 nM (IC50)
[storage]

Store at -20°C
[References]

[1] Wagner FF, et al. Exploiting an Asp-Glu "switch" in glycogen synthase kinase 3 to design paralog-selective inhibitors for use in acute myeloid leukemia. Sci Transl Med. 2018 Mar 7;10(431). pii: eaam8460. DOI:10.1126/scitranslmed.aam8460
Spectrum DetailBack Directory
[Spectrum Detail]

BRD0705(2056261-41-5)1HNMR
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