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| Reaction Details | |||
|---|---|---|---|
 | Report a problem with these data | ||
| Target | Mitogen-activated protein kinase 14 | ||
| Ligand | BDBM50524521 | ||
| Substrate/Competitor | n/a | ||
| Meas. Tech. | ChEMBL_1893918 (CHEMBL4395839) | ||
| IC50 | 18±n/a nM | ||
| Citation |  Heider, F; Ansideri, F; Tesch, R; Pantsar, T; Haun, U; Döring, E; Kudolo, M; Poso, A; Albrecht, W; Laufer, SA; Koch, P Pyridinylimidazoles as dual glycogen synthase kinase 3?/p38? mitogen-activated protein kinase inhibitors. Eur J Med Chem175:309-329 (2019) [PubMed] Article | ||
| More Info.: | Get all data from this article, Assay Method | ||
| Mitogen-activated protein kinase 14 | |||
| Name: | Mitogen-activated protein kinase 14 | ||
| Synonyms: | CSAID-binding protein | CSBP | CSBP1 | CSBP2 | CSPB1 | Cytokine suppressive anti-inflammatory drug-binding protein | MAP kinase 14 | MAP kinase MXI2 | MAP kinase p38 alpha | MAPK 14 | MAPK14 | MAX-interacting protein 2 | MK14_HUMAN | MXI2 | Mitogen-activated protein kinase p38 alpha | SAPK2A | Stress-activated protein kinase 2a | p38 MAP kinase alpha/beta | ||
| Type: | Serine/threonine-protein kinase | ||
| Mol. Mass.: | 41286.76 | ||
| Organism: | Homo sapiens (Human) | ||
| Description: | Q16539 | ||
| Residue: | 360 | ||
| Sequence: |
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| BDBM50524521 | |||
| n/a | |||
| Name | BDBM50524521 | ||
| Synonyms: | CHEMBL4446355 | ||
| Type | Small organic molecule | ||
| Emp. Form. | C20H18ClFN4OS | ||
| Mol. Mass. | 416.9 | ||
| SMILES | CSc1nc(c([nH]1)-c1ccnc(NC(=O)[C@@H]2C[C@H](Cl)C2)c1)-c1ccc(F)cc1 |r,wU:15.15,17.18,(80.61,-5.18,;79.85,-6.51,;78.31,-6.51,;77.56,-5.17,;76.05,-5.47,;75.87,-7,;77.27,-7.65,;74.53,-7.76,;73.21,-6.97,;71.86,-7.72,;71.85,-9.27,;73.18,-10.05,;73.17,-11.59,;74.5,-12.37,;74.48,-13.91,;75.84,-11.61,;77.31,-12.02,;77.72,-10.54,;79.06,-9.78,;76.24,-10.13,;74.52,-9.29,;74.92,-4.44,;75.26,-2.93,;74.13,-1.89,;72.65,-2.35,;71.52,-1.31,;72.32,-3.86,;73.45,-4.9,)| | ||
| Structure | 
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