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| Reaction Details | |||
|---|---|---|---|
 | Report a problem with these data | ||
| Target | Aurora kinase C | ||
| Ligand | BDBM50175305 | ||
| Substrate/Competitor | n/a | ||
| Meas. Tech. | ChEMBL_1628974 (CHEMBL3871600) | ||
| IC50 | 12±n/a nM | ||
| Citation |  Chang, CF; Lin, WH; Ke, YY; Lin, YS; Wang, WC; Chen, CH; Kuo, PC; Hsu, JTA; Uang, BJ; Hsieh, HP Discovery of novel inhibitors of Aurora kinases with indazole scaffold: In silico fragment-based and knowledge-based drug design. Eur J Med Chem124:186-199 (2016) [PubMed] Article | ||
| More Info.: | Get all data from this article, Assay Method | ||
| Aurora kinase C | |||
| Name: | Aurora kinase C | ||
| Synonyms: | AIE2 | AIK3 | AIRK3 | ARK3 | AURKC | AURKC_HUMAN | Aurora Kinase C (Aurora-C) | Aurora kinase C | Aurora kinase C (AURKC) | Aurora-C | Aurora-C/INCENP | Aurora/Ipl1-related kinase 3 | Aurora/Ipl1/Eg2 protein 2 | STK13 | Serine/threonine-protein kinase 13 | Serine/threonine-protein kinase Aurora-C | ||
| Type: | Enzyme | ||
| Mol. Mass.: | 35602.43 | ||
| Organism: | Homo sapiens (Human) | ||
| Description: | Amino acid residues 1-309 were expressed as His-tagged fusion protein using baculovirus expression system. | ||
| Residue: | 309 | ||
| Sequence: |
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| BDBM50175305 | |||
| n/a | |||
| Name | BDBM50175305 | ||
| Synonyms: | CHEMBL3600873 | ||
| Type | Small organic molecule | ||
| Emp. Form. | C22H21ClFN3O3S | ||
| Mol. Mass. | 461.937 | ||
| SMILES | OC(=O)[C@@]1(Cc2cccc(Nc3nccs3)n2)CC[C@@H](CC1)Oc1cccc(Cl)c1F |r,wU:3.2,wD:19.24,(2.4,1.65,;1.33,2.27,;1.34,3.5,;,1.54,;-1.33,2.27,;-2.67,1.5,;-2.64,-.04,;-3.96,-.84,;-5.31,-.09,;-5.34,1.45,;-6.69,2.19,;-8,1.39,;-8.11,-.13,;-9.61,-.48,;-10.41,.83,;-9.4,2,;-4.02,2.24,;1.33,.77,;1.33,-.77,;,-1.54,;-1.33,-.77,;-1.33,.77,;0,-3.08,;1.34,-3.85,;2.67,-3.07,;4.01,-3.84,;4.01,-5.38,;2.68,-6.15,;2.68,-7.39,;1.34,-5.39,;.28,-6.01,)| | ||
| Structure | 
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