BDBM80759 7-[(1-hydroxy-1-phenylpropan-2-yl)amino]quinoline-5,8-dione::7-[(1-oxidanyl-1-phenyl-propan-2-yl)amino]quinoline-5,8-dione::7-[(2-hydroxy-1-methyl-2-phenyl-ethyl)amino]quinoline-5,8-quinone::CHEMBL339439::MLS002702297::SMR001565859::cid_386231

SMILES CC(Nc1cc(O)c2cccnc2c1O)C(=O)c1ccccc1

InChI Key InChIKey=NRNOHSAWMMRPDI-UHFFFAOYSA-N

Data  6 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 6 hits for monomerid = 80759   

TargetHexokinase HKDC1 [W721R](Homo sapiens (Human))
Burnham Center For Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM80759(7-[(1-hydroxy-1-phenylpropan-2-yl)amino]quinoline-...)
Affinity DataIC50:  1.85E+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
In DepthDetails PCBioAssay
TargetHexokinase HKDC1 [W721R](Homo sapiens (Human))
Burnham Center For Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM80759(7-[(1-hydroxy-1-phenylpropan-2-yl)amino]quinoline-...)
Affinity DataIC50:  7.51E+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
In DepthDetails PCBioAssay
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
University Of Pittsburgh

Curated by ChEMBL
LigandPNGBDBM80759(7-[(1-hydroxy-1-phenylpropan-2-yl)amino]quinoline-...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibitory Activity against Recombinant Human PTP1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
University Of Pittsburgh

Curated by ChEMBL
LigandPNGBDBM80759(7-[(1-hydroxy-1-phenylpropan-2-yl)amino]quinoline-...)
Affinity DataIC50:  1.60E+4nMAssay Description:Inhibitory Activity against Recombinant Human VHRMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 2(Homo sapiens (Human))
University Of Pittsburgh

Curated by ChEMBL
LigandPNGBDBM80759(7-[(1-hydroxy-1-phenylpropan-2-yl)amino]quinoline-...)
Affinity DataIC50:  510nMAssay Description:Inhibitory activity against recombinant human cell division cycle 25BMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosyl-DNA phosphodiesterase 2(Homo sapiens (Human))
The Scripps Research Institute Molecular Screening Center

Curated by PubChem BioAssay
LigandPNGBDBM80759(7-[(1-hydroxy-1-phenylpropan-2-yl)amino]quinoline-...)
Affinity DataIC50:  5.45E+3nMAssay Description:Source (MLPCN Center Name): The Scripps Research Institute Molecular Screening Center (SRIMSC) Center Affiliation: The Scripps Research Institute (TS...More data for this Ligand-Target Pair
In DepthDetails PCBioAssay