BDBM50129952 2-(3-(5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-8-yl)-4-hydroxyphenyl)-5,7-dihydroxy-4H-chromen-4-one::8-[5-(5,7-Dihydroxy-4-oxo-4H-chromen-2-yl)-2-hydroxy-phenyl]-5,7-dihydroxy-2-(4-hydroxy-phenyl)-chromen-4-one::Amentoflavone::CHEMBL63354::cid_5281600
SMILES Oc1ccc(cc1)-c1cc(=O)c2c(O)cc(O)c(-c3cc(ccc3O)-c3cc(O)c4c(cc(O)cc4=O)o3)c2o1
InChI Key InChIKey=QYDURWHTEIUTEI-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 82 hits for monomerid = 50129952
Affinity DataIC50: 2.58E+3nMAssay Description:Inhibition of recombinant human MMP9 preincubated for 30 mins followed by McaPro-Leu-Gly-Leu-Dpa-Ala-Arg-NH2 substrate addition measured by fluoresce...More data for this Ligand-Target Pair
TargetProbable nicotinate-nucleotide adenylyltransferase(Staphylococcus aureus subsp. aureus N315)
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Target1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase gamma-1(Bovine)
Seoul National University
Curated by ChEMBL
Seoul National University
Curated by ChEMBL
Affinity DataIC50: 2.90E+4nMAssay Description:Inhibition of bovine brain PI-PLCgamma1More data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human cloned cPLA2 expressed in HEK293 cellsMore data for this Ligand-Target Pair
Target1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase gamma-1(Human)
Seoul National University
Curated by ChEMBL
Seoul National University
Curated by ChEMBL
Affinity DataIC50: 2.90E+4nMAssay Description:Inhibition of PLCgamma1More data for this Ligand-Target Pair
Affinity DataIC50: 1.54E+3nMAssay Description:Inhibition of BACE1 after 60 mins by FRET assayMore data for this Ligand-Target Pair
Affinity DataIC50: 2.38E+4nMAssay Description:Inhibition of sPLA2-2A in HEK293 cellMore data for this Ligand-Target Pair
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Catholic University of Daegu
Curated by ChEMBL
Catholic University of Daegu
Curated by ChEMBL
Affinity DataIC50: 7.40E+3nMAssay Description:Inhibition of human recombinant PTP1B using p-NPP as substrate preincubated for 10 mins followed by substrate addition measured after 20 mins by micr...More data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of rat cloned sPLA2-1B expressed in HEK293 cellsMore data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human cloned sPLA2-10 expressed in HEK293 cellsMore data for this Ligand-Target Pair
Affinity DataIC50: 3.53E+4nMAssay Description:Inhibition of cow milk xanthine oxidaseMore data for this Ligand-Target Pair
Affinity DataKd: 17nMAssay Description:Binding affinity to recombinant VEGFA (unknown origin) measured for 60 seconds by surface plasmon resonance assayMore data for this Ligand-Target Pair
Affinity DataKd: 8.20nMAssay Description:Binding affinity to recombinant PIGF1 (unknown origin) measured for 60 seconds by surface plasmon resonance assayMore data for this Ligand-Target Pair
TargetGamma-aminobutyric acid receptor subunit alpha-1/beta-2/gamma-2(Human)
University of Sydney
Curated by ChEMBL
University of Sydney
Curated by ChEMBL
Affinity DataIC50: 2.82E+8nMAssay Description:logIC50 (30 uM) GABA-A receptor alpha-1-beta-2-gamma-2 subunits expressed in Xenopus oocytesMore data for this Ligand-Target Pair
TargetGamma-aminobutyric acid receptor subunit alpha-1/beta-2/gamma-2(Human)
University of Sydney
Curated by ChEMBL
University of Sydney
Curated by ChEMBL
Affinity DataEC50: 3.60E+3nMAssay Description:Effective concentration against human recombinant GABA-A receptor alpha-1-beta-2-gamma-2 subunits expressed in Xenopus oocytesMore data for this Ligand-Target Pair
Affinity DataIC50: 3.03E+4nMAssay Description:Inhibition of recombinant human MMP2 preincubated for 30 mins followed by McaPro-Leu-Gly-Leu-Dpa-Ala-Arg-NH2 substrate addition measured by fluoresce...More data for this Ligand-Target Pair
TargetTransitional endoplasmic reticulum ATPase(Human)
The Scripps Research Institute Molecular Screening Center
Curated by PubChem BioAssay
The Scripps Research Institute Molecular Screening Center
Curated by PubChem BioAssay
Affinity DataIC50: 8.98E+3nMAssay Description:Source (MLPCN Center Name): The Scripps Research Institute Molecular Screening Center Center Affiliation: The Scripps Research Institute (TSRI) Assay...More data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of recombinant human MMP3 preincubated for 30 mins followed by McaPro-Leu-Gly-Leu-Dpa-Ala-Arg-NH2 substrate addition measured by fluoresce...More data for this Ligand-Target Pair
Affinity DataKd: 2.18E+3nMAssay Description:Binding affinity to MMP9 (unknown origin) by SPR assayMore data for this Ligand-Target Pair
Affinity DataIC50: 1.27E+3nMAssay Description:Inhibition of human neutrophil elastase using N-Methoxysuccinyl-Ala-Ala-Pro-Val-p-nitroanilid as substrate measured after 1 hrMore data for this Ligand-Target Pair
Affinity DataIC50: 1.85E+3nMAssay Description:Inhibition of human Cathepsin KMore data for this Ligand-Target Pair
Affinity DataIC50: 1.19E+5nMAssay Description:Inhibition of HIV1 recombinant reverse transcriptase p66/p51 expressed in Escherichia coliMore data for this Ligand-Target Pair
TargetReplicase polyprotein 1ab(SARS-CoV)
Korea Research Institute of Bioscience and Biotechnology
Curated by ChEMBL
Korea Research Institute of Bioscience and Biotechnology
Curated by ChEMBL
Affinity DataIC50: 8.30E+3nMAssay Description:Inhibition of SARS coronavirus 3C-like protease after 60 mins by FRET assayMore data for this Ligand-Target Pair
Affinity DataIC50: 4.80E+3nMAssay Description:Inhibition of human amyloid beta (1 to 40) assessed as reduction in aggregation measured after 24 hrs by ThT fluorescence assayMore data for this Ligand-Target Pair
Affinity DataIC50: 187nMAssay Description:Inhibition of recombinant human full-length PARP-1 using biotinylated substrateMore data for this Ligand-Target Pair
Affinity DataIC50: 1.03E+4nMAssay Description:Inhibition of recombinant human full-length PARP-2 using biotinylated substrateMore data for this Ligand-Target Pair
Affinity DataIC50: 0.200nMAssay Description:Inhibition of PARP-1 (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 1.03E+4nMAssay Description:Inhibition of PARP-2 (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 120nMAssay Description:Inhibition of PARP1 (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 259nMAssay Description:Inhibition of PARP1 (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 198nMAssay Description:Inhibition of PARP1 (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 1.03E+4nMAssay Description:Inhibition of PARP2 (unknown origin)More data for this Ligand-Target Pair
TargetTransitional endoplasmic reticulum ATPase(Human)
The Scripps Research Institute Molecular Screening Center
Curated by PubChem BioAssay
The Scripps Research Institute Molecular Screening Center
Curated by PubChem BioAssay
Affinity DataIC50: 5.00E+4nMAssay Description:Source (MLPCN Center Name): The Scripps Research Institute Molecular Screening Center Center Affiliation: The Scripps Research Institute (TSRI) Assay...More data for this Ligand-Target Pair
TargetInduced myeloid leukemia cell differentiation protein Mcl-1(Human)
Emory University
Curated by PubChem BioAssay
Emory University
Curated by PubChem BioAssay
Affinity DataIC50: 1.63E+3nMAssay Description:NIH Molecular Libraries Screening Centers Network [MLSCN] Emory Chemical Biology Discovery Center in MLSCN Assay provider: Nikolovska-Coleska, Univer...More data for this Ligand-Target Pair
TargetM1 family aminopeptidase(Plasmodium falciparum (isolate FcB1 / Columbia))
Srmlsc
Curated by PubChem BioAssay
Srmlsc
Curated by PubChem BioAssay
Affinity DataIC50: 1.08E+5nMAssay Description:Southern Research Molecular Libraries Screening Center (SRMLSC) Southern Research Institute (Birmingham, Alabama) NIH Molecular Libraries Screening...More data for this Ligand-Target Pair
Affinity DataEC50: 1.50E+5nMAssay Description:Keywords: Group A streptococcus, GAS, streptokinase, expression, virulence, inhibition, dose response, EC50 Assay Overview: The goal of this assa...More data for this Ligand-Target Pair
TargetGamma-aminobutyric acid receptor subunit alpha-1(Rat)
WestfÄLische Wilhelms-UniversitÄ
Curated by PDSP Ki Database
WestfÄLische Wilhelms-UniversitÄ
Curated by PDSP Ki Database
Affinity DataKi: 36nMAssay Description:Binding affinity to delta opioid receptorMore data for this Ligand-Target Pair
Affinity DataKi: 37nMAssay Description:Binding affinity (in vitro) against Opioid receptor delta 1 using radio-ligand binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 37nMAssay Description:Binding affinity to delta opioid receptorMore data for this Ligand-Target Pair
TargetSodium-dependent dopamine transporter(Bovine)
WestfÄLische Wilhelms-UniversitÄ
Curated by PDSP Ki Database
WestfÄLische Wilhelms-UniversitÄ
Curated by PDSP Ki Database
Affinity DataKi: 1.24E+3nMAssay Description:Binding affinity (in vitro) against Dopamine receptor D3 using radio-ligand binding assayMore data for this Ligand-Target Pair
Target5-hydroxytryptamine receptor 2C(Human)
WestfÄLische Wilhelms-UniversitÄ
Curated by PDSP Ki Database
WestfÄLische Wilhelms-UniversitÄ
Curated by PDSP Ki Database
Target5-hydroxytryptamine receptor 2C(Human)
WestfÄLische Wilhelms-UniversitÄ
Curated by PDSP Ki Database
WestfÄLische Wilhelms-UniversitÄ
Curated by PDSP Ki Database
Affinity DataKi: 2.56E+3nMAssay Description:Binding affinity towards pig 5-hydroxytryptamine 2C receptorMore data for this Ligand-Target Pair
Affinity DataKi: 4.09E+3nMAssay Description:Binding affinity (in vitro) against 5-hydroxytryptamine 1D receptor alpha using radio-ligand binding assayMore data for this Ligand-Target Pair
Target5-hydroxytryptamine receptor 1B(Human)
WestfÄLische Wilhelms-UniversitÄ
Curated by PDSP Ki Database
WestfÄLische Wilhelms-UniversitÄ
Curated by PDSP Ki Database
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Catholic University of Daegu
Curated by ChEMBL
Catholic University of Daegu
Curated by ChEMBL
Affinity DataKi: 7.80E+3nMAssay Description:Mixed-competitive inhibition of human recombinant PTP1B using p-NPP as substrate preincubated for 10 mins followed by substrate addition measured aft...More data for this Ligand-Target Pair
TargetKappa-type opioid receptor(Human)
WestfÄLische Wilhelms-UniversitÄ
Curated by PDSP Ki Database
WestfÄLische Wilhelms-UniversitÄ
Curated by PDSP Ki Database