(Rac)-BRD0705 CAS 1597440-03-3
Introduction:Basic information about (Rac)-BRD0705 CAS 1597440-03-3, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
(Rac)-BRD0705 Basic information
| Product Name: | (Rac)-BRD0705 |
| Synonyms: | (Rac)-BRD0705;GSK3α,inhibit,Racemate,(Rac)BRD0705,GSK-3,Inhibitor,Glycogen synthase kinase-3,(Rac) BRD0705,(Rac)-BRD-0705,Glycogen synthase kinase 3,(Rac)-BRD0705;5H-Pyrazolo[3,4-b]quinolin-5-one, 4-ethyl-1,2,4,6,7,8-hexahydro-7,7-dimethyl-4-phenyl-;(Rac)-BRD0705, 10 mM in DMSO;4-ethyl-7,7-dimethyl-4-phenyl-1,6,8,9-tetrahydropyrazolo[3,4-b]quinolin-5-one |
| CAS: | 1597440-03-3 |
| MF: | C20H23N3O |
| MW: | 321.42 |
| EINECS: | |
| Product Categories: | |
| Mol File: | 1597440-03-3.mol |
(Rac)-BRD0705 Chemical Properties
| Boiling point | 512.0±50.0 °C(Predicted) |
| density | 1.22±0.1 g/cm3(Predicted) |
| form | Solid |
| pka | 14.82±0.60(Predicted) |
| color | Light yellow to yellow |
Safety Information
| Uses | (Rac)-BRD0705 is a less active racemate of BRD0705. 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)[1][2]. |
| 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 [2] Edward Scolnick, et al. Uses of paralog-selective inhibitors of gsk3 kinases. US20160375006A1. |
