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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 34:
Zdrazil B, Felix E, Hunter F, Manners EJ, Blackshaw J, Corbett S, de Veij M, Ioannidis H, Lopez DM, Mosquera JF, Magarinos MP, Bosc N, Arcila R, Kizilören T, Gaulton A, Bento AP, Adasme MF, Monecke P, Landrum GA, Leach AR. (2024). The ChEMBL Database in 2023: a drug discovery platform spanning multiple bioactivity data types and time periods. Nucleic Acids Res., 52(D1). DOI: 10.1093/nar/gkad1004. [EPMCID:10767899] [PMID:37933841]
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]