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ChEMBL ligand: CHEMBL3629013 |
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DB | Assay description | Assay Type | Standard value | Standard parameter | Original value | Original units | Original parameter | Reference |
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mitogen-activated protein kinase 8/c-Jun N-terminal kinase 1 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2276] [GtoPdb: 1496] [UniProtKB: P45983] | ||||||||
ChEMBL | Inhibition of JNK1 (unknown origin) by FRET method | B | 5.98 | pIC50 | 1040 | nM | IC50 | J Med Chem (2015) 58: 8182-8199 [PMID:26431428] |
GtoPdb | - | - | 6 | pIC50 | 1004 | nM | IC50 | J Med Chem (2015) 58: 8182-99 [PMID:26431428] |
mitogen-activated protein kinase 9/c-Jun N-terminal kinase 2 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4179] [GtoPdb: 1497] [UniProtKB: P45984] | ||||||||
ChEMBL | Inhibition of JNK2 (unknown origin) by FRET method | B | 5.3 | pIC50 | 5000 | nM | IC50 | J Med Chem (2015) 58: 8182-8199 [PMID:26431428] |
mitogen-activated protein kinase 10/c-Jun N-terminal kinase 3 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2637] [GtoPdb: 1498] [UniProtKB: P53779] | ||||||||
ChEMBL | Inhibition of JNK3 (unknown origin) by FRET method | B | 5.68 | pIC50 | 2100 | nM | IC50 | J Med Chem (2015) 58: 8182-8199 [PMID:26431428] |
GtoPdb | - | - | 5.68 | pIC50 | 2100 | nM | IC50 | J Med Chem (2015) 58: 8182-99 [PMID:26431428] |
mitogen-activated protein kinase kinase 4/Dual specificity mitogen-activated protein kinase kinase 4 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2897] [GtoPdb: 2065] [UniProtKB: P45985] | ||||||||
GtoPdb | - | - | 5.3 | pIC50 | >5000 | nM | IC50 | J Pharmacol Exp Ther (1997) 283: 636-47 [PMID:9353380] |
ChEMBL | Inhibition of MKK4 (unknown origin) using KFMMTPpYVVTR substrate incubated for 1 hr measured by MpTPpYV probe-based fluorescence polarization assay | B | 5.3 | pIC50 | >5000 | nM | IC50 | J Med Chem (2015) 58: 8182-8199 [PMID:26431428] |
mitogen-activated protein kinase kinase 7/Dual specificity mitogen-activated protein kinase kinase 7 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3530] [GtoPdb: 2068] [UniProtKB: O14733] | ||||||||
GtoPdb | - | - | 5.3 | pIC50 | 5000 | nM | IC50 | J Med Chem (2015) 58: 8182-99 [PMID:26431428] |
ChEMBL | Inhibition of MKK7 (unknown origin) using KFMMTPpYVVTR substrate incubated for 1 hr measured by MpTPpYV probe-based fluorescence polarization assay | B | 5.3 | pIC50 | >5000 | nM | IC50 | J Med Chem (2015) 58: 8182-8199 [PMID:26431428] |
colony stimulating factor 1 receptor/Macrophage colony stimulating factor receptor in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL1844] [GtoPdb: 1806] [UniProtKB: P07333] | ||||||||
ChEMBL | Inhibition of CSF1R (unknown origin) by FRET method | B | 4.24 | pIC50 | 57000 | nM | IC50 | J Med Chem (2015) 58: 8182-8199 [PMID:26431428] |
mitogen-activated protein kinase kinase kinase 10/Mitogen-activated protein kinase kinase kinase 10 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2873] [GtoPdb: 2070] [UniProtKB: Q02779] | ||||||||
ChEMBL | Inhibition of MLK2 (unknown origin) by FRET method | B | 5 | pIC50 | >10000 | nM | IC50 | J Med Chem (2015) 58: 8182-8199 [PMID:26431428] |
mitogen-activated protein kinase kinase kinase 11/Mitogen-activated protein kinase kinase kinase 11 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2708] [GtoPdb: 2071] [UniProtKB: Q16584] | ||||||||
ChEMBL | Inhibition of MLK3 (unknown origin) by FRET method | B | 5 | pIC50 | >10000 | nM | IC50 | J Med Chem (2015) 58: 8182-8199 [PMID:26431428] |
mitogen-activated protein kinase kinase kinase 12/Mitogen-activated protein kinase kinase kinase 12 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL1908389] [GtoPdb: 2072] [UniProtKB: Q12852] | ||||||||
ChEMBL | Inhibition of N-terminally GST- tagged human DLK catalytic domain (1 to 520 amino acids) using N-terminally HIS-tagged MKK4 K131M as substrate incubated for 60 mins by TR-FRET assay | B | 7.38 | pKi | 42 | nM | Ki | J Med Chem (2015) 58: 8182-8199 [PMID:26431428] |
GtoPdb | - | - | 7.38 | pKi | 42 | nM | Ki | J Med Chem (2015) 58: 8182-99 [PMID:26431428] |
ChEMBL | Inhibition of Dox inducible human DLK transfected in HEK293 cells assessed as reduction in JNK phosphorylation incubated for 5.5 hrs measured by Hoechst 33342 staining based imaging analysis | B | 6.27 | pIC50 | 536 | nM | IC50 | J Med Chem (2015) 58: 8182-8199 [PMID:26431428] |
mitogen-activated protein kinase kinase kinase 9/Mitogen-activated protein kinase kinase kinase 9 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2872] [GtoPdb: 2084] [UniProtKB: P80192] | ||||||||
ChEMBL | Inhibition of MLK1 (unknown origin) by FRET method | B | 5 | pIC50 | >10000 | nM | IC50 | J Med Chem (2015) 58: 8182-8199 [PMID:26431428] |
ChEMBL data shown on this page come from version 32:
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]