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| Reaction Details | |||
|---|---|---|---|
 | Report a problem with these data | ||
| Target | Mitogen-activated protein kinase 7 | ||
| Ligand | BDBM50559467 | ||
| Substrate/Competitor | n/a | ||
| Meas. Tech. | ChEMBL_2069575 (CHEMBL4724828) | ||
| IC50 | 131±n/a nM | ||
| Citation |  Sato, M; Kondo, T; Kohno, Y; Seto, S Discovery of benzo[f]pyrido[4,3-b][1,4]oxazepin-10-one derivatives as orally available bromodomain and extra-terminal domain (BET) inhibitors with efficacy in an in vivo psoriatic animal model. Bioorg Med Chem34:0 (2021) [PubMed] Article | ||
| More Info.: | Get all data from this article, Assay Method | ||
| Mitogen-activated protein kinase 7 | |||
| Name: | Mitogen-activated protein kinase 7 | ||
| Synonyms: | BMK1 | Big MAP kinase 1 | ERK5 | Extracellular signal-regulated kinase 5 (ERK5) | MAPK7 | MK07_HUMAN | PRKM7 | ||
| Type: | Protein | ||
| Mol. Mass.: | 88377.36 | ||
| Organism: | Homo sapiens (Human) | ||
| Description: | Q13164 | ||
| Residue: | 816 | ||
| Sequence: |
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| BDBM50559467 | |||
| n/a | |||
| Name | BDBM50559467 | ||
| Synonyms: | CHEMBL4763016 | ||
| Type | Small organic molecule | ||
| Emp. Form. | C19H20FN3O3 | ||
| Mol. Mass. | 357.3788 | ||
| SMILES | CN1c2cnc(N[C@H]3CC[C@H](O)CC3)cc2Oc2cccc(F)c2C1=O |r,wU:7.6,wD:10.10,(51.72,-32.35,;52.07,-33.85,;50.87,-34.83,;49.54,-34.06,;48.21,-34.83,;48.21,-36.37,;46.88,-37.14,;46.88,-38.67,;48.21,-39.44,;48.21,-40.98,;46.87,-41.74,;46.87,-43.28,;45.55,-40.97,;45.55,-39.44,;49.54,-37.14,;50.88,-36.37,;52.1,-37.32,;53.61,-36.96,;54.5,-38.23,;56.04,-38.09,;56.69,-36.68,;55.8,-35.42,;56.44,-34.03,;54.26,-35.56,;53.59,-34.17,;54.53,-32.96,)| | ||
| Structure | 
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