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ChEMBL ligand: CHEMBL685 (Chlorfenson, Emverm, K-6451, Mebendazol, Mebendazole, Mebendazole polymorph c, Mebendazolum, Mebenvet, NSC-184849, NSC-5618, Orthotran, Ovex, Ovitelmin, Ovochlor, Pantelmin, R 17,635, R-17635, Telmin, Telmintic, Vermicidin, Vermox, Zhihuanqing) |
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DB | Assay description | Assay Type | Standard value | Standard parameter | Original value | Original units | Original parameter | Reference |
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Calmodulin-domain protein kinase 1 in Toxoplasma gondii (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL1781862] [UniProtKB: Q9BJF5] | ||||||||
ChEMBL | Inhibition of Toxoplasma gondii CDPK1 | B | 6.17 | pIC50 | 670 | nM | IC50 | Bioorg Med Chem Lett (2012) 22: 5264-5267 [PMID:22795629] |
Methionine aminopeptidase in Escherichia coli (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3423] [UniProtKB: P0AE18] | ||||||||
ChEMBL | Inhibition of Co2+ loaded MetAP expressed in Escherichia coli | B | 5 | pIC50 | >10000 | nM | IC50 | J Med Chem (2006) 49: 511-522 [PMID:16420038] |
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 human ABL by radiometric assay | B | 5.34 | pKi | 4600 | nM | Ki | J Med Chem (2012) 55: 2803-2810 [PMID:22369268] |
ChEMBL | Inhibition of human ABL | B | 5.3 | pIC50 | 5000 | nM | IC50 | Bioorg Med Chem Lett (2012) 22: 5264-5267 [PMID:22795629] |
SRC proto-oncogene, non-receptor tyrosine kinase/Tyrosine-protein kinase SRC in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL267] [GtoPdb: 2206] [UniProtKB: P12931] | ||||||||
ChEMBL | Inhibition of human SRC by radiometric assay | B | 5 | pKi | >10000 | nM | Ki | J Med Chem (2012) 55: 2803-2810 [PMID:22369268] |
ChEMBL | Inhibition of human SRC | B | 5 | pIC50 | >10000 | nM | IC50 | Bioorg Med Chem Lett (2012) 22: 5264-5267 [PMID:22795629] |
kinase insert domain receptor/Vascular endothelial growth factor receptor 2 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL279] [GtoPdb: 1813] [UniProtKB: P35968] | ||||||||
ChEMBL | Inhibition of VEGFR2-mediated angiogenesis in human HUVEC cells after 24 hrs by inverted photomicroscopic analysis | B | 5.06 | pIC50 | 8800 | nM | IC50 | J Med Chem (2012) 55: 6832-6848 [PMID:22780961] |
ChEMBL | Inhibition of human VEGFR2 (789 to 1356 residues) assessed as reduction in autophosphorylation at Y1175 residues using poly (Glu4Tyr1) peptide and ATP as substrate incubated for 60 mins by ADP-Glo Kinase Assay | B | 5.37 | pIC50 | 4300 | nM | IC50 | Eur J Med Chem (2021) 215: 113268-113268 [PMID:33636537] |
ChEMBL | Inhibition of VEGFR2 after 60 mins by electrophoretic mobility shift assay | B | 5.44 | pIC50 | 3600 | nM | IC50 | J Med Chem (2012) 55: 6832-6848 [PMID:22780961] |
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]