BDBM50162328 CHEMBL195166::N-Furan-2-ylmethyl-N''-(3-{[(furan-2-ylmethyl)-aminooxalyl]-amino}-methyl)-benzyl)-oxalamide::cid_2851556
SMILES O=C(NCc1ccco1)C(=O)NCc1cccc(CNC(=O)C(=O)NCc2ccco2)c1
InChI Key InChIKey=CASUHSYWKAPYDI-UHFFFAOYSA-N
Data 7 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 7 hits for monomerid = 50162328
TargetLow molecular weight phosphotyrosine protein phosphatase(Human)
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataIC50: 4.00E+4nMAssay Description:Concentration to inhibit strand transfer of soluble mutant (F185K, C280S) of wild type Human immunodeficiency virus-1 integraseMore data for this Ligand-Target Pair
TargetCarboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 1(Human)
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataIC50: 8.00E+4nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, C...More data for this Ligand-Target Pair
TargetLow molecular weight phosphotyrosine protein phosphatase(Human)
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataIC50: 1.00E+5nMAssay Description:Concentration to inhibit strand transfer of wild type Human immuno deficiency virus-1 integraseMore data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+5nMAssay Description:Concentration to inhibit 3' processing of wild type Human immuno deficiency virus-1 integraseMore data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+6nMAssay Description:Concentration to inhibit 3' processing of soluble mutant (F185K, C280S) of wild type Human immunodeficiency virus-1 integraseMore data for this Ligand-Target Pair
