null

SMILES NS(=O)(=O)c1cccc(c1)-c1nnc(o1)-c1ccc(Cl)cc1

InChI Key InChIKey=WSFBXXSBCRXLBR-UHFFFAOYSA-N

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

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 6 hits for monomerid = 50502792   

TargetCarbonic anhydrase 13(Homo sapiens (Human))TBA
LigandPNGBDBM50502792(CHEMBL4460034)copy SMILEScopy InChI
Affinity DataKi:  16nMAssay Description:Inhibition of recombinant human carbonic anhydrase 13 by stopped flow CO2 hydrase assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X63RMCPubMed
TargetCarbonic anhydrase 9(Homo sapiens (Human))TBA
LigandPNGBDBM50502792(CHEMBL4460034)copy SMILEScopy InChI
Affinity DataKi:  55nMAssay Description:Inhibition of recombinant human carbonic anhydrase 9 by stopped flow CO2 hydrase assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X63RMCPubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50502792(CHEMBL4460034)copy SMILEScopy InChI
Affinity DataKi:  608nMAssay Description:Inhibition of recombinant human carbonic anhydrase 2 by stopped flow CO2 hydrase assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X63RMCPubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))TBA
LigandPNGBDBM50502792(CHEMBL4460034)copy SMILEScopy InChI
Affinity DataKi:  916nMAssay Description:Inhibition of recombinant human carbonic anhydrase 1 by stopped flow CO2 hydrase assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X63RMCPubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Ushinsky Yaroslavl State Pedagogical University

Curated by ChEMBL
LigandPNGBDBM50502792(CHEMBL4460034)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human recombinant MAO-A expressed in insect cells microsomes assessed as inhibition of 4-hydroxyquinoline formation using kynuramine as...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K64NBTPubMed
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
Ushinsky Yaroslavl State Pedagogical University

Curated by ChEMBL
LigandPNGBDBM50502792(CHEMBL4460034)copy SMILEScopy InChI
Affinity DataIC50: 210nMAssay Description:Inhibition of human recombinant MAO-B expressed in insect cells microsomes assessed as inhibition of 4-hydroxyquinoline formation using kynuramine as...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K64NBTPubMed