compound 24 [PMID: 23441572] [Ligand Id: 8147] activity data from GtoPdb and ChEMBL

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ChEMBL ligand: CHEMBL2324924
  • mitogen-activated protein kinase 14/MAP kinase p38 alpha in Human [ChEMBL: CHEMBL260] [GtoPdb: 1499] [UniProtKB: Q16539]
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  • ABL proto-oncogene 1, non-receptor tyrosine kinase/Tyrosine-protein kinase ABL in Human [ChEMBL: CHEMBL1862] [GtoPdb: 1923] [UniProtKB: P00519]
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  • ABL proto-oncogene 2, non-receptor tyrosine kinase/Tyrosine-protein kinase ABL2 in Human [ChEMBL: CHEMBL4014] [GtoPdb: 1924] [UniProtKB: P42684]
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DB Assay description Assay Type Standard value Standard parameter Original value Original units Original parameter Reference
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 (unknown origin) B 7.37 pIC50 43 nM IC50 J Med Chem (2013) 56: 3033-3047 [PMID:23441572]
ABL proto-oncogene 1, non-receptor tyrosine kinase/Tyrosine-protein kinase ABL in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL1862] [GtoPdb: 1923] [UniProtKB: P00519]
ChEMBL Inhibition of Abl1 kinase (unknown origin) using Tyr 6 peptide as substrate assessed as residual enzyme activity after every 10 secs measured for 10 mins B 9 pIC50 1 nM IC50 J Med Chem (2013) 56: 3033-3047 [PMID:23441572]
ChEMBL Inhibition of wild type Abl1 kinase (unknown origin) B 9.22 pIC50 0.6 nM IC50 J Med Chem (2013) 56: 3033-3047 [PMID:23441572]
GtoPdb - - 9.3 pIC50 0.5 nM IC50 J Med Chem (2013) 56: 3033-47 [PMID:23441572]
ChEMBL Inhibition of Abl1 kinase Q252H mutant (unknown origin) B 9.3 pIC50 0.5 nM IC50 J Med Chem (2013) 56: 3033-3047 [PMID:23441572]
ChEMBL Inhibition of Abl1 kinase T315I mutant (unknown origin) B 9.4 pIC50 0.4 nM IC50 J Med Chem (2013) 56: 3033-3047 [PMID:23441572]
ChEMBL Inhibition of Abl1 kinase Y253F mutant (unknown origin) B 9.52 pIC50 0.3 nM IC50 J Med Chem (2013) 56: 3033-3047 [PMID:23441572]
ChEMBL Inhibition of Abl1 kinase M351T mutant (unknown origin) B 9.52 pIC50 0.3 nM IC50 J Med Chem (2013) 56: 3033-3047 [PMID:23441572]
ChEMBL Inhibition of Abl1 kinase H396P mutant (unknown origin) B 9.52 pIC50 0.3 nM IC50 J Med Chem (2013) 56: 3033-3047 [PMID:23441572]
ChEMBL Inhibition of Abl1 kinase (unknown origin) using Tyr 6 peptide as substrate assessed as residual enzyme activity after every 10 secs measured for 10 mins by platform assay B 9.7 pIC50 0.2 nM IC50 J Med Chem (2013) 56: 3033-3047 [PMID:23441572]
ABL proto-oncogene 2, non-receptor tyrosine kinase/Tyrosine-protein kinase ABL2 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4014] [GtoPdb: 1924] [UniProtKB: P42684]
ChEMBL Inhibition of Abl2 kinase (unknown origin) using Tyr 6 peptide as substrate assessed as residual enzyme activity after every 10 secs measured for 10 mins by platform assay B 8.7 pIC50 2 nM IC50 J Med Chem (2013) 56: 3033-3047 [PMID:23441572]
GtoPdb - - 9 pIC50 1 nM IC50 J Med Chem (2013) 56: 3033-47 [PMID:23441572]
ChEMBL Inhibition of Abl2 kinase (unknown origin) using Tyr 6 peptide as substrate assessed as residual enzyme activity after every 10 secs measured for 10 mins B 9 pIC50 1 nM IC50 J Med Chem (2013) 56: 3033-3047 [PMID:23441572]

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]