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| Reaction Details | |||
|---|---|---|---|
 | Report a problem with these data | ||
| Target | Glycogen synthase kinase-3 alpha | ||
| Ligand | BDBM50424226 | ||
| 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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| BDBM50424226 | |||
| n/a | |||
| Name | BDBM50424226 | ||
| Synonyms: | CHEMBL2314102 | ||
| Type | Small organic molecule | ||
| Emp. Form. | C22H16N4O2S | ||
| Mol. Mass. | 400.453 | ||
| SMILES | COc1ccccc1-c1c(C#N)c(N)nc2sc(C(=O)c3ccccc3)c(N)c12 |(2.87,-6.42,;4.21,-7.18,;5.54,-6.4,;5.53,-4.87,;6.86,-4.1,;8.2,-4.85,;8.2,-6.39,;6.87,-7.16,;6.87,-8.7,;5.54,-9.47,;4.21,-8.69,;2.87,-7.92,;5.54,-11.02,;4.21,-11.79,;6.87,-11.79,;8.21,-11.02,;9.68,-11.5,;10.59,-10.24,;12.13,-10.24,;12.9,-8.91,;12.91,-11.57,;12.13,-12.91,;12.9,-14.24,;14.44,-14.24,;15.21,-12.89,;14.44,-11.57,;9.68,-8.99,;10.16,-7.52,;8.21,-9.47,)| | ||
| Structure | 
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