BDBM14672 2-hydroxypropane-1,2,3-tricarboxylic acid::CHEMBL1261::CITRIC ACID::Citrate::Citric Acid::Fragment 2::cid_311
SMILES OC(=O)CC(O)(CC(O)=O)C(O)=O
InChI Key InChIKey=KRKNYBCHXYNGOX-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 16 hits for monomerid = 14672
Affinity DataKi: 4.90E+5nMpH: 5.0Assay Description:Inhibition of Bacillus licheniformis BS3 beta-lactamase at pH 5More data for this Ligand-Target Pair
Affinity DataIC50: 8.00E+5nMAssay Description:Inhibition of KDM5B (unknown origin)More data for this Ligand-Target Pair
TargetPerilipin-1(Human)
The Scripps Research Institute Molecular Screening Center
Curated by PubChem BioAssay
The Scripps Research Institute Molecular Screening Center
Curated by PubChem BioAssay
TargetPerilipin-5(Human)
The Scripps Research Institute Molecular Screening Center
Curated by PubChem BioAssay
The Scripps Research Institute Molecular Screening Center
Curated by PubChem BioAssay
Target3-dehydroquinate dehydratase(Helicobacter pylori (strain ATCC 700392 / 26695) (...)
University of Glasgow
Curated by ChEMBL
University of Glasgow
Curated by ChEMBL
Affinity DataKd: 2.50E+3nMAssay Description:Binding affinity for Helicobacter pylori DHQase 2More data for this Ligand-Target Pair
Affinity DataKd: 7.30E+3nMAssay Description:Binding affinity for Streptomyces coelicolor DHQase 2More data for this Ligand-Target Pair
Affinity DataIC50: 3.00E+5nMAssay Description:Inhibition of human hexahistidine-tagged full-length FTO expressed in Escherichia coli BL21 (DE3) using 3-methylthymidine as substrate assessed as in...More data for this Ligand-Target Pair
Affinity DataIC50: 2.13E+5nMAssay Description:Inhibition of N-terminal His6-tagged recombinant Paramecium bursaria chlorella virus 1 CPH expressed in Escherichia coli Rosetta 2 (DE3) cells pre-in...More data for this Ligand-Target Pair
Affinity DataIC50: 4.88E+5nMAssay Description:Inhibition of N-terminal His-tagged recombinant human ALKBH5 catalytic AlkB domain (74 to 294 residues) transfected in Escherichia coli BL21-V2R-pRAR...More data for this Ligand-Target Pair
Affinity DataIC50: 6.28E+5nMAssay Description:Inhibition of recombinant human ALKBH5 catalytic AlkB domain (74 to 294 residues) transfected in Escherichia coli BL21 (DE3) using 8-mer m6A-ssDNA as...More data for this Ligand-Target Pair
Affinity DataIC50: 8.50E+5nMAssay Description:Inhibition of human FIH expressed in H5 insect cellsMore data for this Ligand-Target Pair
Affinity DataIC50: 6.30E+6nMAssay Description:Inhibition of human PHD1 expressed in H5 insect cellsMore data for this Ligand-Target Pair
Affinity DataIC50: 4.80E+6nMAssay Description:Inhibition of human PHD2 expressed in H5 insect cellsMore data for this Ligand-Target Pair
Affinity DataIC50: 5.50E+5nMAssay Description:Inhibition of human PHD3 expressed in H5 insect cellsMore data for this Ligand-Target Pair
Affinity DataIC50: >4.00E+7nMpH: 7.4 T: 22°CAssay Description:SPA uses 125I as energy donor and scintillant-coated beads as energy acceptor. The labeled ligand is captured by the biotinylated Src-SH2 protein imm...More data for this Ligand-Target Pair
TargetHepatocyte nuclear factor 4-alpha(Human)
The Scripps Research Institute Molecular Screening Center
Curated by PubChem BioAssay
The Scripps Research Institute Molecular Screening Center
Curated by PubChem BioAssay