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ChEMBL ligand: CHEMBL471901 |
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DB | Assay description | Assay Type | Standard value | Standard parameter | Original value | Original units | Original parameter | Reference |
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calcium/calmodulin dependent protein kinase ID/CaM kinase I delta in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL5073] [GtoPdb: 1953] [UniProtKB: Q8IU85] | ||||||||
ChEMBL | Inhibition of human CAMK1D using KKALRRQETVDAL as substrate in presence of [gamma-33P]-ATP by hotspot kinase assay | B | 6.34 | pIC50 | 456 | nM | IC50 | J Med Chem (2020) 63: 6784-6801 [PMID:32433887] |
ChEMBL | Inhibition of recombinant human full-length His-tagged CAMK1D expressed in baculovirus expression system using autocamtide-2 as substrate preincubated for 15 mins followed by ATP addition and measured after 2 hrs by ADP-glo luminescence assay | B | 6.36 | pIC50 | 432 | nM | IC50 | J Med Chem (2020) 63: 6784-6801 [PMID:32433887] |
Lysyl-tRNA synthetase in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL5575] [UniProtKB: Q15046] | ||||||||
ChEMBL | Inhibition of human Syk | B | 7.39 | pIC50 | 41 | nM | IC50 | Bioorg Med Chem (2008) 16: 7347-7357 [PMID:18585046] |
spleen associated tyrosine kinase/Tyrosine-protein kinase SYK in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2599] [GtoPdb: 2230] [UniProtKB: P43405] | ||||||||
ChEMBL | Inhibition of SYK | B | 7.39 | pIC50 | 41 | nM | IC50 | Bioorg Med Chem Lett (2008) 18: 6231-6235 [PMID:18938080] |
ChEMBL | Inhibition of recombinant Syk | B | 7.39 | pIC50 | 41 | nM | IC50 | Bioorg Med Chem Lett (2009) 19: 1944-1949 [PMID:19254842] |
ChEMBL | Inhibition of spleen tyrosine kinase (unknown origin) | B | 7.39 | pIC50 | 41 | nM | IC50 | Eur J Med Chem (2013) 67: 434-446 [PMID:23917087] |
GtoPdb | - | - | 7.39 | pIC50 | 41 | nM | IC50 | Bioorg Med Chem (2005) 13: 4936-51 [PMID:15990316] |
ChEMBL | Inhibition of human SYK using poly[Glu:Tyr] (4:1) as substrate in presence of [gamma-33P]-ATP by hotspot kinase assay | B | 8.15 | pIC50 | 7 | nM | IC50 | J Med Chem (2020) 63: 6784-6801 [PMID:32433887] |
zeta chain of T cell receptor associated protein kinase 70/Tyrosine-protein kinase ZAP-70 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2803] [GtoPdb: 2285] [UniProtKB: P43403] | ||||||||
GtoPdb | - | - | 4.95 | pIC50 | 11200 | nM | IC50 | Bioorg Med Chem (2005) 13: 4936-51 [PMID:15990316] |
ChEMBL | Inhibition of human ZAP70 | B | 4.95 | pIC50 | 11200 | nM | IC50 | Bioorg Med Chem (2008) 16: 7347-7357 [PMID:18585046] |
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]