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(Rac)-BRD0705

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CAS:1597440-03-3
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CAS:1597440-03-3
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CAS:1597440-03-3
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(Rac)-BRD0705 manufacturers

  • (Rac)-BRD0705
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  • $88.00 / 1mg
  • 2024-11-19
  • CAS:1597440-03-3
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  • Purity: 99.67%
  • Supply Ability: 10g
  • (Rac)-BRD0705
  • (Rac)-BRD0705 pictures
  • $88.00 / 1mg
  • 2024-11-19
  • CAS:1597440-03-3
  • Min. Order:
  • Purity: 99.67%
  • Supply Ability: 10g
(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
CAS:1597440-03-3
MF:C20H23N3O
MW:321.42
EINECS:
Product Categories:
Mol File:1597440-03-3.mol
(Rac)-BRD0705 Structure
(Rac)-BRD0705 Chemical Properties
Boiling point 512.0±50.0 °C(Predicted)
density 1.22±0.1 g/cm3(Predicted)
pka14.82±0.60(Predicted)
form Solid
color Light yellow to yellow
Safety Information
MSDS Information
(Rac)-BRD0705 Usage And Synthesis
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.
(Rac)-BRD0705 Preparation Products And Raw materials
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