GSK-3 inhibitor X   Click here for help

GtoPdb Ligand ID: 5975

Synonyms: indirubin deriv. 8a [3]
Compound class: Synthetic organic
Comment: Please note that ChEMBL represents this compound as a tautomer of our structure.
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2D Structure
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Physico-chemical Properties
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Hydrogen bond acceptors 4
Hydrogen bond donors 2
Rotatable bonds 3
Topological polar surface area 79.79
Molecular weight 397.01
XLogP 3.66
No. Lipinski's rules broken 0
SMILES / InChI / InChIKey
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Canonical SMILES CC(=O)ONC1=c2ccccc2=NC1=C1C(=O)Nc2c1ccc(c2)Br
Isomeric SMILES CC(=O)ONC1=c2ccccc2=N/C/1=C/1\C(=O)Nc2c1ccc(c2)Br
InChI InChI=1S/C18H12BrN3O3/c1-9(23)25-22-16-12-4-2-3-5-13(12)20-17(16)15-11-7-6-10(19)8-14(11)21-18(15)24/h2-8,22H,1H3,(H,21,24)/b17-15-
InChI Key ORWSYHWTBSHFIV-ICFOKQHNSA-N
Bioactivity Comments
The primary target for this compound is GSK3. The publicly available data use GSK3 (as a complex of α and β isozymes) isolated from pig brain [3].
Selectivity at enzymes
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Target Sp. Type Action Value Parameter Concentration range (M) Reference
glycogen synthase kinase 3 alpha Pig Inhibitor Inhibition 8.0 pIC50 - 3
pIC50 8.0 (IC50 1x10-8 M) [3]
Description: Measured using GSK3 as a complex of α and β isozymes, isolated from pig brain
glycogen synthase kinase 3 beta Pig Inhibitor Inhibition 8.0 pIC50 - 3
pIC50 8.0 (IC50 1x10-8 M) [3]
Description: Measured using GSK3 as a complex of α and β isozymes, isolated from pig brain