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| ChEMBL ligand: CHEMBL3040440 (PND-1186, SR-2516, Vs-4718, VS-4718) |
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| DB | Assay description | Assay Type | Standard value | Standard parameter | Original value | Original units | Original parameter | Reference |
|---|---|---|---|---|---|---|---|---|
| protein tyrosine kinase 2/Focal adhesion kinase 1 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2695] [GtoPdb: 2180] [UniProtKB: Q05397] | ||||||||
| GtoPdb | - | - | 8.82 | pIC50 | 1.5 | nM | IC50 | Cancer Biol Ther (2010) 9: 764-77 [PMID:20234191] |
| ChEMBL | Inhibition of GST-FAK catalytic domain region (411-686) (unknown origin) expressed in baculovirus infected Sf9 cells by spectrophotometry | B | 8.82 | pIC50 | 1.5 | nM | IC50 | ACS Med Chem Lett (2021) 12: 30-38 [PMID:33488961] |
| ChEMBL | Inhibition of GST-fused FAK (411 to 686 residues) (unknown origin) expressed in sf9 cells using poly(Glu:Tyr) (4:1) copolymer as substrate by spectrophotometric method | B | 8.82 | pIC50 | 1.5 | nM | IC50 | J Med Chem (2020) 63: 14382-14403 [PMID:33058670] |
| ChEMBL | Inhibition of GST-fused His-tagged recombinant FAK KD (411 to 686 residues) (unknown origin) expressed in baculovirus infected Sf9 cells using poly(Glu:Tyr) as substrate in presence of ATP by coomassie blue staining based ELISA screening assay | B | 8.82 | pIC50 | 1.5 | nM | IC50 | Cancer Biol Ther (2010) 9: 764-777 [PMID:20234191] |
| mitogen-activated protein kinase 10/Mitogen-activated protein kinase 10 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2637] [GtoPdb: 1498] [UniProtKB: P53779] | ||||||||
| ChEMBL | Inhibition of JNK3 (unknown origin) using biotinylated ATF2 by HTRF method | B | 6.8 | pIC50 | 160 | nM | IC50 | Medchemcomm (2012) 3: 238-243 |
| mitogen-activated protein kinase 9/Mitogen-activated protein kinase 9 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4179] [GtoPdb: 1497] [UniProtKB: P45984] | ||||||||
| ChEMBL | Inhibition of JNK2 (unknown origin) using biotinylated ATF2 by HTRF method | B | 6.92 | pIC50 | 120 | nM | IC50 | Medchemcomm (2012) 3: 238-243 |
ChEMBL data shown on this page come from version 36:
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]