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| Reaction Details | |||
|---|---|---|---|
 | Report a problem with these data | ||
| Target | Mitogen-activated protein kinase 7 | ||
| Ligand | BDBM50559472 | ||
| Substrate/Competitor | n/a | ||
| Meas. Tech. | ChEMBL_2069575 (CHEMBL4724828) | ||
| IC50 | 1100±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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| BDBM50559472 | |||
| n/a | |||
| Name | BDBM50559472 | ||
| Synonyms: | CHEMBL4758899 | ||
| Type | Small organic molecule | ||
| Emp. Form. | C20H23N3O4 | ||
| Mol. Mass. | 369.4143 | ||
| SMILES | COc1cccc2c1Oc1cc(N[C@H]3CC[C@H](O)CC3)ncc1N(C)C2=O |r,wU:13.13,wD:16.17,(37.79,-40.16,;39.32,-40.03,;39.96,-38.64,;41.5,-38.5,;42.16,-37.09,;41.27,-35.83,;39.73,-35.97,;39.08,-37.37,;37.57,-37.73,;36.35,-36.78,;35.01,-37.55,;33.68,-36.78,;32.35,-37.55,;32.35,-39.09,;33.68,-39.85,;33.67,-41.39,;32.34,-42.16,;32.33,-43.69,;31.01,-41.38,;31.02,-39.85,;33.68,-35.24,;35.01,-34.47,;36.34,-35.24,;37.54,-34.26,;37.18,-32.76,;39.05,-34.58,;40,-33.37,)| | ||
| Structure | 
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