BDBM50262062 4-(4-phenyl-1H-1,2,3-triazol-1-yl)benzenesulfonamide::CHEMBL513184

SMILES NS(=O)(=O)c1ccc(cc1)-n1cc(nn1)-c1ccccc1

InChI Key InChIKey=JUKNQYMAQLBMLX-UHFFFAOYSA-N

Data  12 KI  2 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 14 hits for monomerid = 50262062   

TargetCarbonic anhydrase 12(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50262062(4-(4-phenyl-1H-1,2,3-triazol-1-yl)benzenesulfonami...)
Affinity DataKi:  6nMAssay Description:Inhibition of human carbonic anhydrase 12 pre-incubated for 15 mins by stopped flow carbon dioxide hydrase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 12(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50262062(4-(4-phenyl-1H-1,2,3-triazol-1-yl)benzenesulfonami...)
Affinity DataKi:  6nMAssay Description:Inhibition of recombinant human carbonic anhydrase 12 preincubated for 15 mins by stopped-flow CO2 hydrase AssayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Griffith University

Curated by ChEMBL
LigandPNGBDBM50262062(4-(4-phenyl-1H-1,2,3-triazol-1-yl)benzenesulfonami...)
Affinity DataKi:  7.90nMAssay Description:Inhibition of human cloned CA2 by CO2 hydration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 5B, mitochondrial(Homo sapiens (Human))
Griffith University

Curated by ChEMBL
LigandPNGBDBM50262062(4-(4-phenyl-1H-1,2,3-triazol-1-yl)benzenesulfonami...)
Affinity DataKi:  10.6nMAssay Description:Inhibition of human recombinant CA5B by CO2 hydration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 5A, mitochondrial(Homo sapiens (Human))
Griffith University

Curated by ChEMBL
LigandPNGBDBM50262062(4-(4-phenyl-1H-1,2,3-triazol-1-yl)benzenesulfonami...)
Affinity DataKi:  17.8nMAssay Description:Inhibition of human recombinant CA5A by CO2 hydration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 9(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50262062(4-(4-phenyl-1H-1,2,3-triazol-1-yl)benzenesulfonami...)
Affinity DataKi:  26nMAssay Description:Inhibition of recombinant human carbonic anhydrase 9 preincubated for 15 mins by stopped-flow CO2 hydrase AssayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 9(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50262062(4-(4-phenyl-1H-1,2,3-triazol-1-yl)benzenesulfonami...)
Affinity DataKi:  26nMAssay Description:Inhibition of human carbonic anhydrase 9 pre-incubated for 15 mins by stopped flow carbon dioxide hydrase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Griffith University

Curated by ChEMBL
LigandPNGBDBM50262062(4-(4-phenyl-1H-1,2,3-triazol-1-yl)benzenesulfonami...)
Affinity DataKi:  44nMAssay Description:Inhibition of recombinant human carbonic anhydrase 2 preincubated for 15 mins by stopped-flow CO2 hydrase AssayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Griffith University

Curated by ChEMBL
LigandPNGBDBM50262062(4-(4-phenyl-1H-1,2,3-triazol-1-yl)benzenesulfonami...)
Affinity DataKi:  44nMAssay Description:Inhibition of human carbonic anhydrase 2 pre-incubated for 15 mins by stopped flow carbon dioxide hydrase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50262062(4-(4-phenyl-1H-1,2,3-triazol-1-yl)benzenesulfonami...)
Affinity DataKi:  342nMAssay Description:Inhibition of human carbonic anhydrase 1 pre-incubated for 15 mins by stopped flow carbon dioxide hydrase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50262062(4-(4-phenyl-1H-1,2,3-triazol-1-yl)benzenesulfonami...)
Affinity DataKi:  392nMAssay Description:Inhibition of recombinant human carbonic anhydrase 1 preincubated for 15 mins by stopped-flow CO2 hydrase AssayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50262062(4-(4-phenyl-1H-1,2,3-triazol-1-yl)benzenesulfonami...)
Affinity DataKi:  5.10E+3nMAssay Description:Inhibition of human cloned CA1 by CO2 hydration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 1(Ovis aries (Sheep))
University Of Alberta

Curated by ChEMBL
LigandPNGBDBM50262062(4-(4-phenyl-1H-1,2,3-triazol-1-yl)benzenesulfonami...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of ovine COX1 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
University Of Alberta

Curated by ChEMBL
LigandPNGBDBM50262062(4-(4-phenyl-1H-1,2,3-triazol-1-yl)benzenesulfonami...)
Affinity DataIC50:  1.30E+3nMAssay Description:Inhibition of human recombinant COX2 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed