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ChEMBL ligand: CHEMBL47386 ((-)-Epigallocatechin, Epigallocatechin) |
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DB | Assay description | Assay Type | Standard value | Standard parameter | Original value | Original units | Original parameter | Reference |
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aldo-keto reductase family 1 member B/Aldose reductase in Rat (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2622] [GtoPdb: 2768] [UniProtKB: P07943] | ||||||||
ChEMBL | Inhibition of aldose reductase in rat lens homogenate | B | 4.52 | pIC50 | >30000 | nM | IC50 | J Nat Prod (2003) 66: 1191-1196 [PMID:14510595] |
synuclein alpha/Alpha-synuclein in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL6152] [GtoPdb: 3285] [UniProtKB: P37840] | ||||||||
ChEMBL | Inhibition of human alpha-synuclein filament formation expressed in Escherichia coli BL21(DE3) cells incubated for 72 hrs by thioflavin S based fluorescence assay | B | 4.97 | pIC50 | 10600 | nM | IC50 | Eur J Med Chem (2019) 167: 10-36 [PMID:30743095] |
BCL2 apoptosis regulator/Apoptosis regulator Bcl-2 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4860] [GtoPdb: 2844] [UniProtKB: P10415] | ||||||||
ChEMBL | Binding affinity to BCL2 | B | 4 | pKi | >100000 | nM | Ki | Proc Natl Acad Sci U S A (2007) 104: 19512-19517 [PMID:18040043] |
ChEMBL | Displacement of NLWAAQRYGRELRRMSD-K(FITC)-FVD from Bcl-2 (unknown origin) by fluorescence polarization assay | B | 4 | pKi | >100000 | nM | Ki | Med Chem Res (2010) 19: 817-835 |
CB1 receptor/Cannabinoid CB1 receptor in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL218] [GtoPdb: 56] [UniProtKB: P21554] | ||||||||
ChEMBL | Displacement of [3H]-CP55940 from CB1 receptor (unknown origin) | B | 4.45 | pKi | 35700 | nM | Ki | J Nat Prod (2019) 82: 636-646 [PMID:30816712] |
DNA repair protein RAD52 homolog in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2362978] [UniProtKB: P43351] | ||||||||
ChEMBL | Inhibition of RAD52 (unknown origin) assessed as effect on RAD52-mediated annealing of complementary oligonucleotides using T-28 ssDNA substrate by FRET assay | B | 5.31 | pIC50 | 4900 | nM | IC50 | US-20180209956-A1. HTS Assay for Identifying Small Molecule Inhibitors of RAD52 and Uses of Identified Small Molecule Inhibitors for Treatment and Prevention of BRCA-Deficient Malignancies (2018) |
ChEMBL | Inhibition of RAD52 (unknown origin) assessed as effect on RAD52-mediated annealing of complementary oligonucleotides using T-28 ssDNA substrate in presence of replication protein A by FRET assay | B | 5.32 | pIC50 | 4800 | nM | IC50 | US-20180209956-A1. HTS Assay for Identifying Small Molecule Inhibitors of RAD52 and Uses of Identified Small Molecule Inhibitors for Treatment and Prevention of BRCA-Deficient Malignancies (2018) |
ChEMBL | Inhibition of RAD52 (unknown origin) assessed as reduction in RAD52-ssDNA interaction using Cy3-dT30-Cy5 ssDNA by FRET assay | B | 5.74 | pIC50 | 1800 | nM | IC50 | US-20180209956-A1. HTS Assay for Identifying Small Molecule Inhibitors of RAD52 and Uses of Identified Small Molecule Inhibitors for Treatment and Prevention of BRCA-Deficient Malignancies (2018) |
ChEMBL | Inhibition of 6His-tagged human RD52 assessed as reduction in RD52 binding to Cy3-dT30-Cy5 ssDNA incubated for 30 mins by FRET assay | B | 5.74 | pIC50 | 1800 | nM | IC50 | J Med Chem (2020) 63: 14151-14183 [PMID:33135887] |
ChEMBL | Inhibition of RAD52 (unknown origin) assessed as reduction in RAD52-ssDNA interaction using Cy3-dT30-Cy5 ssDNA in presence of replication protein A by FRET assay | B | 5.8 | pIC50 | 1600 | nM | IC50 | US-20180209956-A1. HTS Assay for Identifying Small Molecule Inhibitors of RAD52 and Uses of Identified Small Molecule Inhibitors for Treatment and Prevention of BRCA-Deficient Malignancies (2018) |
Enoyl-[acyl-carrier-protein] reductase in Escherichia coli (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL1857] [UniProtKB: P0AEK4] | ||||||||
ChEMBL | Inhibition of Escherichia coli ENR | B | 4 | pIC50 | >100000 | nM | IC50 | J Med Chem (2007) 50: 765-775 [PMID:17263522] |
Enoyl-acyl-carrier protein reductase in Plasmodium falciparum (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4150] [UniProtKB: Q965D5] | ||||||||
ChEMBL | Inhibition of Plasmodium falciparum ENR using NADH substrate | B | 5.43 | pKi | 3750 | nM | Ki | J Med Chem (2007) 50: 765-775 [PMID:17263522] |
ChEMBL | Inhibition of Plasmodium falciparum ENR using crotonyl-CoA substrate | B | 5.7 | pKi | 2000 | nM | Ki | J Med Chem (2007) 50: 765-775 [PMID:17263522] |
ChEMBL | Inhibition of Plasmodium falciparum ENR in presence of triclosan | B | 7.76 | pKi | 17.56 | nM | Ki | J Med Chem (2007) 50: 765-775 [PMID:17263522] |
ChEMBL | Inhibition of Plasmodium falciparum ENR | B | 5.15 | pIC50 | 7000 | nM | IC50 | J Med Chem (2007) 50: 765-775 [PMID:17263522] |
NAD kinase in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL6177] [UniProtKB: O95544] | ||||||||
ChEMBL | Inhibition of NADK (unknown origin) by HPLC analysis | B | 4 | pIC50 | >100000 | nM | IC50 | ACS Med Chem Lett (2022) 13: 1699-1706 [PMID:36385933] |
Ribonuclease HI in Escherichia coli (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL1770039] [UniProtKB: P0A7Y4] | ||||||||
ChEMBL | Inhibition of Escherichia coli recombinant ribonuclease H after 30 mins by FRET quenching assay | B | 4.7 | pIC50 | >20000 | nM | IC50 | Bioorg Med Chem Lett (2011) 21: 2840-2844 [PMID:21489793] |
ChEMBL | Inhibition of Escherichia coli recombinant ribonuclease H after 30 mins by FRET quenching assay | B | 4.7 | pIC50 | >20000 | nM | IC50 | Bioorg Med Chem Lett (2011) 21: 2840-2844 [PMID:21489793] |
xanthine dehydrogenase/Xanthine dehydrogenase in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL1929] [GtoPdb: 2646] [UniProtKB: P47989] | ||||||||
ChEMBL | Inhibition of xanthine oxidase assessed as decrease in uric acid production by spectrophotometry | B | 4 | pIC50 | >100000 | nM | IC50 | J Nat Prod (1998) 61: 71-76 [PMID:9461655] |
TAS2R39 in Human [GtoPdb: 675] [UniProtKB: P59534] | ||||||||
GtoPdb | - | - | 3.4 | pEC50 | 395500 | nM | EC50 | Biochem Biophys Res Commun (2011) 405: 620-5 [PMID:21272567] |
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]