compound 16 [PMID: 17480064] [Ligand Id: 8177] activity data from GtoPdb and ChEMBL

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ChEMBL ligand: CHEMBL226403
  • MAPK activated protein kinase 2/MAP kinase-activated protein kinase 2 in Human [ChEMBL: CHEMBL2208] [GtoPdb: 2094] [UniProtKB: P49137]
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  • MAPK activated protein kinase 3/MAP kinase-activated protein kinase 3 in Human [ChEMBL: CHEMBL4670] [GtoPdb: 2095] [UniProtKB: Q16644]
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  • MAPK activated protein kinase 5/MAP kinase-activated protein kinase 5 in Human [ChEMBL: CHEMBL3094] [GtoPdb: 2096] [UniProtKB: Q8IW41]
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  • mitogen-activated protein kinase 1/MAP kinase ERK2 in Human [ChEMBL: CHEMBL4040] [GtoPdb: 1495] [UniProtKB: P28482]
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  • MAPK interacting serine/threonine kinase 1/MAP kinase-interacting serine/threonine-protein kinase MNK1 in Human [ChEMBL: CHEMBL4718] [GtoPdb: 2104] [UniProtKB: Q9BUB5]
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  • mitogen-activated protein kinase 14/MAP kinase p38 alpha in Human [ChEMBL: CHEMBL260] [GtoPdb: 1499] [UniProtKB: Q16539]
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DB Assay description Assay Type Standard value Standard parameter Original value Original units Original parameter Reference
MAPK activated protein kinase 2/MAP kinase-activated protein kinase 2 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2208] [GtoPdb: 2094] [UniProtKB: P49137]
GtoPdb - - 8.07 pIC50 8.5 nM IC50 J Med Chem (2007) 50: 2647-54 [PMID:17480064]
ChEMBL Inhibition of MK2 B 8.07 pIC50 8.5 nM IC50 J Med Chem (2007) 50: 2647-2654 [PMID:17480064]
ChEMBL Inhibition of human recombinant MK2 expressed in Escherichia coli BL21(DE3) after 60 mins B 8.07 pIC50 8.5 nM IC50 J Med Chem (2008) 51: 6225-6229 [PMID:18771253]
ChEMBL Inhibition of MK2 pretreated for 30 mins before substrate addition measured after 2 hrs by IMAP assay B 7.31 pEC50 49 nM EC50 Bioorg Med Chem Lett (2011) 21: 3818-3822 [PMID:21565500]
MAPK activated protein kinase 3/MAP kinase-activated protein kinase 3 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4670] [GtoPdb: 2095] [UniProtKB: Q16644]
ChEMBL Inhibition of MK3 B 6.68 pIC50 210 nM IC50 J Med Chem (2007) 50: 2647-2654 [PMID:17480064]
GtoPdb - - 6.68 pIC50 210 nM IC50 J Med Chem (2007) 50: 2647-54 [PMID:17480064]
MAPK activated protein kinase 5/MAP kinase-activated protein kinase 5 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3094] [GtoPdb: 2096] [UniProtKB: Q8IW41]
GtoPdb - - 6.09 pIC50 810 nM IC50 J Med Chem (2007) 50: 2647-54 [PMID:17480064]
ChEMBL Inhibition of MAPKAPK5 (unknown origin) B 7 pIC50 100 nM IC50 J Med Chem (2013) 56: 6991-7002 [PMID:23937569]
ChEMBL Inhibition of MK5 B 7.09 pIC50 81 nM IC50 J Med Chem (2007) 50: 2647-2654 [PMID:17480064]
mitogen-activated protein kinase 1/MAP kinase ERK2 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4040] [GtoPdb: 1495] [UniProtKB: P28482]
ChEMBL Inhibition of ERK2 B 5.46 pIC50 3440 nM IC50 J Med Chem (2007) 50: 2647-2654 [PMID:17480064]
MAPK interacting serine/threonine kinase 1/MAP kinase-interacting serine/threonine-protein kinase MNK1 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4718] [GtoPdb: 2104] [UniProtKB: Q9BUB5]
ChEMBL Inhibition of MNK1 B 5.24 pIC50 5700 nM IC50 J Med Chem (2007) 50: 2647-2654 [PMID:17480064]
mitogen-activated protein kinase 14/MAP kinase p38 alpha in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL260] [GtoPdb: 1499] [UniProtKB: Q16539]
ChEMBL Inhibition of p38alpha B 4 pIC50 >100000 nM IC50 J Med Chem (2007) 50: 2647-2654 [PMID:17480064]

ChEMBL data shown on this page come from version 33:

Mendez D, Gaulton A, Bento AP, Chambers J, De Veij M, Félix E, Magariños MP, Mosquera JF, Mutowo P, Nowotka M, Gordillo-Marañón M, Hunter F, Junco L, Mugumbate G, Rodriguez-Lopez M, Atkinson F, Bosc N, Radoux CJ, Segura-Cabrera A, Hersey A, Leach AR. (2019) 'ChEMBL: towards direct deposition of bioassay data' Nucleic Acids Res., 47(D1). DOI: 10.1093/nar/gky1075. [EPMCID:30398643]
Davies M, Nowotka M, Papadatos G, Dedman N, Gaulton A, Atkinson F, Bellis L, Overington JP. (2015) 'ChEMBL web services: streamlining access to drug discovery data and utilities.' Nucleic Acids Res., 43(W1). DOI: 10.1093/nar/gkv352. [EPMCID:25883136]