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| Reaction Details | |||
|---|---|---|---|
 | Report a problem with these data | ||
| Target | Glycogen synthase kinase-3 alpha | ||
| Ligand | BDBM50424224 | ||
| Substrate/Competitor | n/a | ||
| Meas. Tech. | ChEMBL_934468 (CHEMBL2321415) | ||
| IC50 | >100000±n/a nM | ||
| Citation |  Fugel, W; Oberholzer, AE; Gschloessl, B; Dzikowski, R; Pressburger, N; Preu, L; Pearl, LH; Baratte, B; Ratin, M; Okun, I; Doerig, C; Kruggel, S; Lemcke, T; Meijer, L; Kunick, C 3,6-Diamino-4-(2-halophenyl)-2-benzoylthieno[2,3-b]pyridine-5-carbonitriles are selective inhibitors of Plasmodium falciparum glycogen synthase kinase-3. J Med Chem56:264-75 (2013) [PubMed] Article | ||
| More Info.: | Get all data from this article, Assay Method | ||
| Glycogen synthase kinase-3 alpha | |||
| Name: | Glycogen synthase kinase-3 alpha | ||
| Synonyms: | GSK-3 alpha | GSK3A | GSK3A_HUMAN | Glycogen synthase kinase 3 alpha (GSKalpha) | Glycogen synthase kinase-3 | Glycogen synthase kinase-3 alpha | Glycogen synthase kinase-3 alpha (GSK3 Alpha) | Glycogen synthase kinase-3 alpha (GSK3A) | Glycogen synthase kinase-3 alpha (GSK3alpha) | ||
| Type: | Enzyme | ||
| Mol. Mass.: | 50991.79 | ||
| Organism: | Homo sapiens (Human) | ||
| Description: | P49840 | ||
| Residue: | 483 | ||
| Sequence: |
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| BDBM50424224 | |||
| n/a | |||
| Name | BDBM50424224 | ||
| Synonyms: | CHEMBL2313850 | ||
| Type | Small organic molecule | ||
| Emp. Form. | C21H12BrClN4OS | ||
| Mol. Mass. | 483.768 | ||
| SMILES | Nc1c(sc2nc(N)c(C#N)c(-c3ccccc3Br)c12)C(=O)c1cccc(Cl)c1 |(50.21,-49.5,;49.73,-50.97,;50.65,-52.22,;49.74,-53.48,;48.26,-53,;46.93,-53.77,;45.59,-53,;44.26,-53.77,;45.6,-51.45,;44.26,-50.67,;42.93,-49.9,;46.92,-50.68,;46.91,-49.15,;48.25,-48.38,;48.24,-46.84,;46.91,-46.07,;45.57,-46.85,;45.58,-48.39,;44.25,-49.17,;48.26,-51.45,;52.19,-52.22,;52.96,-50.89,;52.96,-53.56,;52.18,-54.89,;52.95,-56.22,;54.49,-56.22,;55.26,-54.88,;56.8,-54.87,;54.49,-53.55,)| | ||
| Structure | 
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