BRD0705
- Product Name
- BRD0705
- CAS No.
- 2056261-41-5
- Chemical Name
- BRD0705
- Synonyms
- BRD0705;BRD0705 ,S9638;BRD0705 (BRD-0705;BRD0705, 10 mM in DMSO;(4S)-4-ethyl-7,7-dimethyl-4-phenyl-1,6,8,9-tetrahydropyrazolo[3,4-b]quinolin-5-one;(S)-4-Ethyl-7,7-dimethyl-4-phenyl-4,6,7,8-tetrahydro-1H-pyrazolo[3,4-b]quinolin-5(2H)-one;5H-Pyrazolo[3,4-b]quinolin-5-one, 4-ethyl-1,2,4,6,7,8-hexahydro-7,7-dimethyl-4-phenyl-, (4S)-;β-catenin,Glycogen synthase kinase 3,leukemia,Acute,survival,BRD-0705,inhibit,Inhibitor,oral,BRD0705,myeloid,Glycogen synthase kinase-3,bioavailability,BRD 0705,GSK-3,kinase
- CBNumber
- CB24667681
- Molecular Formula
- C20H23N3O
- Formula Weight
- 321.42
- MOL File
- 2056261-41-5.mol
BRD0705 Property
- 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
N-Bromosuccinimide Price
- Product number
- Axon2931
- Product name
- BRD0705
- Purity
- 99%
- Packaging
- 5mg
- Price
- $231
- Updated
- 2021/12/16
- Product number
- CS-0066622
- Product name
- BRD0705
- Purity
- 98.41%
- Packaging
- 5mg
- Price
- $650
- Updated
- 2021/12/16
- Product number
- Axon2931
- Product name
- BRD0705
- Purity
- 99%
- Packaging
- 25mg
- Price
- $781
- Updated
- 2021/12/16
- Product number
- CS-0066622
- Product name
- BRD0705
- Purity
- 98.41%
- Packaging
- 10mg
- Price
- $1050
- Updated
- 2021/12/16
- Product number
- CS-0066622
- Product name
- BRD0705
- Purity
- 98.41%
- Packaging
- 50mg
- Price
- $2950
- Updated
- 2021/12/16
BRD0705 Chemical Properties,Usage,Production
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)
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
BRD0705 Preparation Products And Raw materials
Raw materials
Preparation Products
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