null

SMILES CCCCCCOc1ccc(NC2=C(Cl)C(=O)c3cccnc3C2=O)cc1

InChI Key InChIKey=MEGQGRDKTAMKGE-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50106502   

TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
University of Pittsburgh

Curated by ChEMBL
LigandPNGBDBM50106502(6-Chloro-7-(4-hexyloxy-phenylamino)-quinoline-5,8-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory Activity against Recombinant Human VHRMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X34WR5PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
University of Pittsburgh

Curated by ChEMBL
LigandPNGBDBM50106502(6-Chloro-7-(4-hexyloxy-phenylamino)-quinoline-5,8-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory Activity against Recombinant Human PTP1More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X34WR5PubMed
TargetM-phase inducer phosphatase 2(Homo sapiens (Human))
University of Pittsburgh

Curated by ChEMBL
LigandPNGBDBM50106502(6-Chloro-7-(4-hexyloxy-phenylamino)-quinoline-5,8-...)copy SMILEScopy InChI
Affinity DataIC50: 930nMAssay Description:Inhibitory activity against recombinant human cell division cycle 25BMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X34WR5PubMed