Reaction Details |
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Target | Mitogen-activated protein kinase 3 |
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Ligand | BDBM50164693 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_304950 (CHEMBL826978) |
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IC50 | >1000±n/a nM |
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Citation | Verma, S; Nagarathnam, D; Shao, J; Zhang, L; Zhao, J; Wang, Y; Li, T; Mull, E; Enyedy, I; Wang, C; Zhu, Q; Altieri, M; Jordan, J; Dang, TT; Reddy, S Substituted aminobenzimidazole pyrimidines as cyclin-dependent kinase inhibitors. Bioorg Med Chem Lett15:1973-7 (2005) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Mitogen-activated protein kinase 3 |
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Name: | Mitogen-activated protein kinase 3 |
Synonyms: | ERK1 | ERK1/ERK2 | Extracellular signal-regulated kinase 1 | Extracellular signal-regulated kinase 1 (ERK1) | MAP kinase ERK1 | MAPK3 | MAPK3/MAPK7 | MK03_HUMAN | Mitogen-activated protein kinase | Mitogen-activated protein kinase 3 | PRKM3 |
Type: | Protein |
Mol. Mass.: | 43136.58 |
Organism: | Homo sapiens (Human) |
Description: | curated by PDB 4QTB |
Residue: | 379 |
Sequence: | MAAAAAQGGGGGEPRRTEGVGPGVPGEVEMVKGQPFDVGPRYTQLQYIGEGAYGMVSSAY
DHVRKTRVAIKKISPFEHQTYCQRTLREIQILLRFRHENVIGIRDILRASTLEAMRDVYI
VQDLMETDLYKLLKSQQLSNDHICYFLYQILRGLKYIHSANVLHRDLKPSNLLINTTCDL
KICDFGLARIADPEHDHTGFLTEYVATRWYRAPEIMLNSKGYTKSIDIWSVGCILAEMLS
NRPIFPGKHYLDQLNHILGILGSPSQEDLNCIINMKARNYLQSLPSKTKVAWAKLFPKSD
SKALDLLDRMLTFNPNKRITVEEALAHPYLEQYYDPTDEPVAEEPFTFAMELDDLPKERL
KELIFQETARFQPGVLEAP
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BDBM50164693 |
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n/a |
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Name | BDBM50164693 |
Synonyms: | CHEMBL194721 | N*2*-(3H-Benzoimidazol-5-yl)-N*4*-(2-chloro-phenyl)-5-trifluoromethyl-pyrimidine-2,4-diamine |
Type | Small organic molecule |
Emp. Form. | C18H12ClF3N6 |
Mol. Mass. | 404.776 |
SMILES | FC(F)(F)c1cnc(Nc2ccc3nc[nH]c3c2)nc1Nc1ccccc1Cl |
Structure |
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