null
SMILES O[C@H]1[C@H](Oc2cc3oc(cc(=O)c3c(O)c2O)-c2ccccc2)O[C@@H]([C@@H](O)[C@@H]1O)C(O)=O
InChI Key InChIKey=IKIIZLYTISPENI-ZFORQUDYSA-N
PDB links: 3 PDB IDs match this monomer.
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 22 hits for monomerid = 50242173
TargetATP-binding cassette sub-family C member 2(Rattus norvegicus)
University of Tokyo
Curated by ChEMBL
University of Tokyo
Curated by ChEMBL
Affinity DataKi: 7.95E+3nMAssay Description:TP_TRANSPORTER: inhibition of DNP-SG uptake in bile canalicular membrane vesicles from SD ratMore data for this Ligand-Target Pair
TargetCytochrome P450 1A2(Homo sapiens (Human))
Department of Chemistry, Tripura University, Suryamaninagar 799022, Tripura, India. Electronic address: dindabtu@gmail.com.
Curated by ChEMBL
Department of Chemistry, Tripura University, Suryamaninagar 799022, Tripura, India. Electronic address: dindabtu@gmail.com.
Curated by ChEMBL
Affinity DataKi: 2.54E+4nMAssay Description:Mixed-type inhibition of CYP1A2 in pooled human liver microsomes using varying levels of phenacetin as substrate pretreated for 5 mins followed by su...More data for this Ligand-Target Pair
Affinity DataIC50: 2.00E+5nMAssay Description:Displacement of [3H]LSD from human 5HT7 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
TargetProlyl endopeptidase(Homo sapiens (Human))
Institut de Recerca Biomèdica de Barcelona
Curated by ChEMBL
Institut de Recerca Biomèdica de Barcelona
Curated by ChEMBL
Affinity DataIC50: 1.20E+4nMAssay Description:Inhibition of human brain prolyl oligopeptidase expressed in Escherichia coliMore data for this Ligand-Target Pair
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Institut de Recerca Biomèdica de Barcelona
Curated by ChEMBL
Institut de Recerca Biomèdica de Barcelona
Curated by ChEMBL
Affinity DataIC50: 2.25E+5nMAssay Description:Inhibition of DPP4 (unknown origin)More data for this Ligand-Target Pair
TargetProlyl endopeptidase(Homo sapiens (Human))
Institut de Recerca Biomèdica de Barcelona
Curated by ChEMBL
Institut de Recerca Biomèdica de Barcelona
Curated by ChEMBL
Affinity DataIC50: 1.23E+4nMAssay Description:Inhibition of human recombinant POPMore data for this Ligand-Target Pair
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
China Pharmaceutical University
Curated by ChEMBL
China Pharmaceutical University
Curated by ChEMBL
Affinity DataIC50: 3.55E+3nMAssay Description:Inhibition of LSD1 (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+6nMAssay Description:Inhibition of trypsin-induced elevation in PAI1 production in HUVEC by ELISAMore data for this Ligand-Target Pair
Affinity DataIC50: 6.41E+3nMAssay Description:This is a review article. Please point to the original journal.More data for this Ligand-Target Pair
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
China Pharmaceutical University
Curated by ChEMBL
China Pharmaceutical University
Curated by ChEMBL
Affinity DataIC50: 3.01E+3nMAssay Description:Inhibition of LSD1 (unknown origin) expressed in human MGC-803 cells incubated for 5 days by DAPI staining based immunofluorescence methodMore data for this Ligand-Target Pair
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
China Pharmaceutical University
Curated by ChEMBL
China Pharmaceutical University
Curated by ChEMBL
Affinity DataIC50: 3.01E+3nMAssay Description:Inhibition of LSD1 (unknown origin)More data for this Ligand-Target Pair
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
China Pharmaceutical University
Curated by ChEMBL
China Pharmaceutical University
Curated by ChEMBL
Affinity DataIC50: 3.01E+3nMAssay Description:Mean functional activity against human H3 receptorMore data for this Ligand-Target Pair
In DepthDetails
Affinity DataIC50: 1.22E+4nMAssay Description:The kinase assay was performed using the EMD Millipore KinaseProfiler service assay protocol. Aurora B kinase was supplied by EMD Millipore Corp. The...More data for this Ligand-Target Pair
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
Dalian University of Technology
Curated by ChEMBL
Dalian University of Technology
Curated by ChEMBL
Affinity DataIC50: 1.44E+4nMAssay Description:Inhibition of Cdk1/cyclin BMore data for this Ligand-Target Pair