Reaction Details | |||
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Target | Aurora kinase B | ||
Ligand | BDBM50191398 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | ChEMBL_445190 (CHEMBL894338) | ||
IC50 | 10000±n/a nM | ||
Citation | Myrianthopoulos, V; Magiatis, P; Ferandin, Y; Skaltsounis, AL; Meijer, L; Mikros, E An integrated computational approach to the phenomenon of potent and selective inhibition of aurora kinases B and C by a series of 7-substituted indirubins. J Med Chem50:4027-37 (2007) [PubMed] Article | ||
More Info.: | Get all data from this article, Assay Method | ||
Aurora kinase B | |||
Name: | Aurora kinase B | ||
Synonyms: | AIK2 | AIM-1 | AIM1 | AIRK2 | ARK2 | AURKB | AURKB_HUMAN | Aurora B kinase (aurB) | Aurora B-INCENP | Aurora kinase 2 | Aurora kinase B (AURKB) | Aurora-related kinase 2 | STK-1 | STK1 | STK12 | STK5 | Serine/threonine-protein kinase aurora B | ||
Type: | Protein | ||
Mol. Mass.: | 39327.72 | ||
Organism: | Homo sapiens (Human) | ||
Description: | Q96GD4 | ||
Residue: | 344 | ||
Sequence: |
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BDBM50191398 | |||
n/a | |||
Name | BDBM50191398 | ||
Synonyms: | (2'Z,3'E)-7-iodoindirubin-3'-oxime | CHEMBL209648 | ||
Type | Small organic molecule | ||
Emp. Form. | C16H10IN3O2 | ||
Mol. Mass. | 403.174 | ||
SMILES | Oc1[nH]c2c(I)cccc2c1-c1[nH]c2ccccc2c1N=O |(26.57,-40.82,;27.04,-39.35,;28.5,-38.87,;28.49,-37.34,;29.64,-36.32,;31.1,-36.79,;29.32,-34.82,;27.85,-34.35,;26.72,-35.37,;27.04,-36.86,;26.14,-38.11,;24.6,-38.11,;23.69,-39.38,;22.21,-38.9,;20.87,-39.67,;19.53,-38.9,;19.53,-37.35,;20.87,-36.58,;22.2,-37.35,;23.68,-36.86,;24.15,-35.38,;23.11,-34.25,)| | ||
Structure |