| Reaction Details |
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 | Report a problem with these data |
| Target | MAP kinase-activated protein kinase 3 |
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| Ligand | BDBM50509949 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | ChEMBL_1839788 (CHEMBL4340003) |
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| IC50 | >10000±n/a nM |
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| Citation |  Sun, C; Fang, L; Zhang, X; Gao, P; Gou, S Novel 7-formyl-naphthyridyl-ureas derivatives as potential selective FGFR4 inhibitors: Design, synthesis, and biological activity studies. Bioorg Med Chem27:1932-1941 (2019) [PubMed] Article |
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| More Info.: | Get all data from this article, Assay Method |
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| MAP kinase-activated protein kinase 3 |
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| Name: | MAP kinase-activated protein kinase 3 |
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| Synonyms: | 3pK | Chromosome 3p kinase | MAP kinase-activated protein kinase 3 (MAPKAP-K3) | MAPK-Activated Protein Kinase 3 (MK3) | MAPK-activated protein kinase 3 | MAPK3_HUMAN | MAPKAP kinase 3 | MAPKAPK-3 | MAPKAPK3 |
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| Type: | Serine/threonine-protein kinase |
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| Mol. Mass.: | 42991.57 |
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| Organism: | Homo sapiens (Human) |
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| Description: | Recombinant MAPKAPK3 was phosphorylated by incubation with active p38alpha before assays. |
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| Residue: | 382 |
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| Sequence: | MDGETAEEQGGPVPPPVAPGGPGLGGAPGGRREPKKYAVTDDYQLSKQVLGLGVNGKVLE
CFHRRTGQKCALKLLYDSPKARQEVDHHWQASGGPHIVCILDVYENMHHGKRCLLIIMEC
MEGGELFSRIQERGDQAFTEREAAEIMRDIGTAIQFLHSHNIAHRDVKPENLLYTSKEKD
AVLKLTDFGFAKETTQNALQTPCYTPYYVAPEVLGPEKYDKSCDMWSLGVIMYILLCGFP
PFYSNTGQAISPGMKRRIRLGQYGFPNPEWSEVSEDAKQLIRLLLKTDPTERLTITQFMN
HPWINQSMVVPQTPLHTARVLQEDKDHWDEVKEEMTSALATMRVDYDQVKIKDLKTSNNR
LLNKRRKKQAGSSSASQGCNNQ
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| BDBM50509949 |
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| n/a |
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| Name | BDBM50509949 |
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| Synonyms: | CHEMBL4475216 | US11667631, Example 29 |
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| Type | Small organic molecule |
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| Emp. Form. | C26H31N7O5 |
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| Mol. Mass. | 521.5682 |
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| SMILES | COC[C@@H](C)Nc1cc(NC(=O)N2CCCc3cc(CN4CCCCOC4=O)c(C=O)nc23)ncc1C#N |r| |
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| Structure | 
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