Reaction Details |
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Target | Mitogen-activated protein kinase 1 |
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Ligand | BDBM50205363 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1524687 (CHEMBL3631081) |
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Kd | 247000±n/a nM |
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Citation | Burdick, DJ; Wang, S; Heise, C; Pan, B; Drummond, J; Yin, J; Goeser, L; Magnuson, S; Blaney, J; Moffat, J; Wang, W; Chen, H Fragment-based discovery of potent ERK2 pyrrolopyrazine inhibitors. Bioorg Med Chem Lett25:4728-32 (2015) [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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BDBM50205363 |
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n/a |
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Name | BDBM50205363 |
Synonyms: | 6-(benzylamino)purine | 6-BAP | 6-[(phenylmethyl)amino]-9H-purine | BAP | CHEMBL228862 | Cytokinin B | N(6)-(benzylamino)purine | N-benzyl-9H-purin-6-amine | N-benzyladenine | benzyladenine |
Type | Small organic molecule |
Emp. Form. | C12H11N5 |
Mol. Mass. | 225.2492 |
SMILES | C(Nc1ncnc2nc[nH]c12)c1ccccc1 |
Structure |
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