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ChEMBL ligand: CHEMBL290376 (DuP-714) |
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DB | Assay description | Assay Type | Standard value | Standard parameter | Original value | Original units | Original parameter | Reference |
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plasminogen/Plasminogen in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL1801] [GtoPdb: 2394] [UniProtKB: P00747] | ||||||||
ChEMBL | In vitro for inhibition of plasmin | B | 8.29 | pKi | 5.1 | nM | Ki | Bioorg Med Chem Lett (1996) 6: 2913-2918 |
coagulation factor II, thrombin/Thrombin in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL204] [GtoPdb: 2362] [UniProtKB: P00734] | ||||||||
ChEMBL | Binding affinity against Thrombin. | B | 10.39 | pKd | 0.04 | nM | Kd | J Med Chem (2000) 43: 305-341 [PMID:10669559] |
ChEMBL | Inhibition of Coagulation factor II | B | 10.38 | pKi | 0.04 | nM | Ki | Bioorg Med Chem Lett (1999) 9: 925-930 [PMID:10230612] |
ChEMBL | Inhibition constant for binding with thrombin was determined | B | 10.39 | pKi | 0.04 | nM | Ki | J Med Chem (1993) 36: 1831-1838 [PMID:8515421] |
ChEMBL | In vitro for inhibition of thrombin. | B | 10.39 | pKi | 0.04 | nM | Ki | Bioorg Med Chem Lett (1996) 6: 2913-2918 |
GtoPdb | Affinity for thrombin active site. | - | 10.39 | pKi | 0.04 | nM | Ki | Bioorg Med Chem Lett (1996) 6: 2913–2918 |
ChEMBL | Inhibition of thrombin | B | 10.4 | pKi | 0.04 | nM | Ki | Bioorg Med Chem Lett (1997) 7: 1595-1600 |
ChEMBL | Inhibition of compound against thrombin mediated platelet activation and fibrinogen cleavage. | B | 10.4 | pKi | 0.04 | nM | Ki | J Med Chem (2000) 43: 305-341 [PMID:10669559] |
Thrombin in Bovine (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4471] [UniProtKB: P00735] | ||||||||
ChEMBL | Concentration necessary to double time for clot formation induced by bovine thrombin | B | 7.26 | pKi | 55 | nM | Ki | Bioorg Med Chem Lett (1996) 6: 2913-2918 |
plasminogen activator, tissue type/Tissue-type plasminogen activator in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL1873] [GtoPdb: 2392] [UniProtKB: P00750] | ||||||||
GtoPdb | - | - | 8.24 | pKi | 5.7 | nM | Ki | Bioorg Med Chem Lett (1996) 6: 2913–2918 |
ChEMBL | Compound was tested in vitro for inhibition of tissue plasminogen activator | B | 8.24 | pKi | 5.7 | nM | Ki | Bioorg Med Chem Lett (1996) 6: 2913-2918 |
serine protease 1/Trypsin I in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL209] [GtoPdb: 2397] [UniProtKB: P07477] | ||||||||
ChEMBL | Inhibitory activity against trypsin | B | 8.05 | pKi | 9 | nM | Ki | Bioorg Med Chem Lett (1999) 9: 925-930 [PMID:10230612] |
ChEMBL | Inhibition of trypsin | B | 10.35 | pKi | 0.04 | nM | Ki | Bioorg Med Chem Lett (1997) 7: 1595-1600 |
ChEMBL | Binding affinity against Trypsin | B | 10.35 | pKi | 0.04 | nM | Ki | J Med Chem (2000) 43: 305-341 [PMID:10669559] |
ChEMBL | Compound was tested in vitro for inhibition of trypsin | B | 10.35 | pKi | 0.04 | nM | Ki | Bioorg Med Chem Lett (1996) 6: 2913-2918 |
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]