inamrinone [Ligand Id: 7202] activity data from GtoPdb and ChEMBL

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ChEMBL ligand: CHEMBL12856 (Amcoral, Amrinone, C01CE01, Cartonic, Cordemcura, Inamrinone, NSC-759805, Vesistol, WIN 40680, WIN-40680, Wincoram)
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  • TTK protein kinase/Dual specificity protein kinase TTK in Human [ChEMBL: CHEMBL3983] [GtoPdb: 2264] [UniProtKB: P33981]
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  • aurora kinase A/Serine/threonine-protein kinase Aurora-A in Human [ChEMBL: CHEMBL4722] [GtoPdb: 1936] [UniProtKB: O14965]
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  • phosphodiesterase 3A in Human [GtoPdb: 1298] [UniProtKB: Q14432]
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  • phosphodiesterase 3B in Human [GtoPdb: 1299] [UniProtKB: Q13370]
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DB Assay description Assay Type Standard value Standard parameter Original value Original units Original parameter Reference
aurora kinase B/Aurora kinase B/Inner centromere protein in Human (target type: PROTEIN COMPLEX) [ChEMBL: CHEMBL3430907] [GtoPdb: 1937] [UniProtKB: Q96GD4Q9NQS7]
ChEMBL Inhibition of human full length N-terminal GST-tagged Aurora B (1 to 344 end residues)/His-tagged INCENP (803 to 918 end residues) expressed in baculovirus expression system using fluorescence-labeled FL-Peptide 21 as substrate after 60 mins in presence of ATP by fluorescence assay based Cheng-Prusoff equation analysis B 4.23 pKi 59300 nM Ki Bioorg Med Chem (2018) 26: 3021-3029 [PMID:29764757]
TTK protein kinase/Dual specificity protein kinase TTK in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3983] [GtoPdb: 2264] [UniProtKB: P33981]
ChEMBL Inhibition of full length human Mps1 using fluorescence-labeled H236 peptide as substrate after 60 to 90 mins in presence of ATP by fluorescence assay based Cheng-Prusoff equation analysis B 4.09 pKi 80800 nM Ki Bioorg Med Chem (2018) 26: 3021-3029 [PMID:29764757]
aurora kinase A/Serine/threonine-protein kinase Aurora-A in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4722] [GtoPdb: 1936] [UniProtKB: O14965]
ChEMBL Inhibition of full length N-terminal His-tagged Aurora A (unknown origin) using fluorescence-labeled FL-Peptide 21 as substrate after 60 mins in presence of ATP by fluorescence assay based Cheng-Prusoff equation analysis B 3.4 pKi 393900 nM Ki Bioorg Med Chem (2018) 26: 3021-3029 [PMID:29764757]
phosphodiesterase 3A in Human [GtoPdb: 1298] [UniProtKB: Q14432]
GtoPdb Inhibition of PDE3 purified from human platelets, and therefore assumed to be the PDE3A subtype. - 4.8 pIC50 16000 nM IC50 J Med Chem (1989) 32: 342-50 [PMID:2536438]
phosphodiesterase 3B in Human [GtoPdb: 1299] [UniProtKB: Q13370]
GtoPdb - - 4.51 pIC50 31200 nM IC50 Biochem Pharmacol (2000) 59: 347-56 [PMID:10644042]

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]