Reaction Details |
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Target | Mitogen-activated protein kinase 1 |
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Ligand | BDBM50021767 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1368653 |
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IC50 | 445±n/a nM |
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Citation | Blake, JF; Gaudino, JJ; De Meese, J; Mohr, P; Chicarelli, M; Tian, H; Garrey, R; Thomas, A; Siedem, CS; Welch, MB; Kolakowski, G; Kaus, R; Burkard, M; Martinson, M; Chen, H; Dean, B; Dudley, DA; Gould, SE; Pacheco, P; Shahidi-Latham, S; Wang, W; West, K; Yin, J; Moffat, J; Schwarz, JB Discovery of 5,6,7,8-tetrahydropyrido[3,4-d]pyrimidine inhibitors of Erk2. Bioorg Med Chem Lett24:2635-9 (2014) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Mitogen-activated protein kinase 1 |
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Name: | Mitogen-activated protein kinase 1 |
Synonyms: | ERK2 | ERT1 | Extracellular signal-regulated kinase 2 | Extracellular signal-regulated kinase 2 (ERK-2) | Extracellular signal-regulated kinase 2 (ERK2) | MAP Kinase 2/ERK2 | MAPK 2 | MAPK1 | MK01_HUMAN | Mitogen activated kinase 1 (ERK-2) | Mitogen-activated protein kinase 1 (ERK-2) | Mitogen-activated protein kinase 1 (ERK2) | Mitogen-activated protein kinase 2 | PRKM1 | PRKM2 | p42-MAPK |
Type: | Ser/Thr Protein Kinase |
Mol. Mass.: | 41392.76 |
Organism: | Homo sapiens (Human) |
Description: | P28482 |
Residue: | 360 |
Sequence: | MAAAAAAGAGPEMVRGQVFDVGPRYTNLSYIGEGAYGMVCSAYDNVNKVRVAIKKISPFE
HQTYCQRTLREIKILLRFRHENIIGINDIIRAPTIEQMKDVYIVQDLMETDLYKLLKTQH
LSNDHICYFLYQILRGLKYIHSANVLHRDLKPSNLLLNTTCDLKICDFGLARVADPDHDH
TGFLTEYVATRWYRAPEIMLNSKGYTKSIDIWSVGCILAEMLSNRPIFPGKHYLDQLNHI
LGILGSPSQEDLNCIINLKARNYLLSLPHKNKVPWNRLFPNADSKALDLLDKMLTFNPHK
RIEVEQALAHPYLEQYYDPSDEPIAEAPFKFDMELDDLPKEKLKELIFEETARFQPGYRS
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BDBM50021767 |
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n/a |
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Name | BDBM50021767 |
Synonyms: | CHEMBL3298677 |
Type | Small organic molecule |
Emp. Form. | C22H22ClFN6O2 |
Mol. Mass. | 456.9 |
SMILES | Cc1cc(Nc2ncc3CCN(Cc3n2)C(=O)N[C@H](CO)c2ccc(F)c(Cl)c2)ccn1 |r| |
Structure |
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