BDBM50334349 4-(3-(3-nitrophenyl)ureido)benzenesulfonamide::4-{[(3'-Nitrophenyl)carbamoyl]amino}benzenesulfonamide::4-{[(3-nitrophenyl)carbamoyl]amino}benzenesulfonamide::CA IX inhibitor, (C)1::CHEMBL1614844

SMILES NS(=O)(=O)c1ccc(NC(=O)Nc2cccc(c2)[N+]([O-])=O)cc1

InChI Key InChIKey=MTGVDZIMBQRGPD-UHFFFAOYSA-N

Data  18 KI

PDB links: 1 PDB ID matches this monomer.

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 18 hits for monomerid = 50334349   

TargetCarbonic anhydrase 9(Homo sapiens (Human))
University Of Florida College Of Medicine

Curated by ChEMBL
LigandPNGBDBM50334349(4-(3-(3-nitrophenyl)ureido)benzenesulfonamide | 4-...)
Affinity DataKi:  0.900nMAssay Description:Inhibition of human carbonic anhydrase 9 for 15 mins by stopped flow CO2 hydration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 9(Homo sapiens (Human))
University Of Florida College Of Medicine

Curated by ChEMBL
LigandPNGBDBM50334349(4-(3-(3-nitrophenyl)ureido)benzenesulfonamide | 4-...)
Affinity DataKi:  0.900nMAssay Description:The inhibition constants (Ki) of FEC to four human CA isoenzymes I, II, IX and XII were determined by CA catalyzed CO2 hydration assays following pre...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 9(Homo sapiens (Human))
University Of Florida College Of Medicine

Curated by ChEMBL
LigandPNGBDBM50334349(4-(3-(3-nitrophenyl)ureido)benzenesulfonamide | 4-...)
Affinity DataKi:  0.900nMAssay Description:Inhibition of human CA9 by stopped-flow CO2 hydrase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 9(Homo sapiens (Human))
University Of Florida College Of Medicine

Curated by ChEMBL
LigandPNGBDBM50334349(4-(3-(3-nitrophenyl)ureido)benzenesulfonamide | 4-...)
Affinity DataKi:  0.900nMAssay Description:Inhibition of tumor-associated human carbonic anhydrase 9 preincubated for 15 min by CO2 hydration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 12(Homo sapiens (Human))
Universita` Degli Studi Di Firenze

Curated by ChEMBL
LigandPNGBDBM50334349(4-(3-(3-nitrophenyl)ureido)benzenesulfonamide | 4-...)
Affinity DataKi:  5.70nMAssay Description:Inhibition of tumor-associated human carbonic anhydrase 12 preincubated for 15 min by CO2 hydration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 12(Homo sapiens (Human))
Universita` Degli Studi Di Firenze

Curated by ChEMBL
LigandPNGBDBM50334349(4-(3-(3-nitrophenyl)ureido)benzenesulfonamide | 4-...)
Affinity DataKi:  5.70nMAssay Description:Inhibition of human carbonic anhydrase 12 for 15 mins by stopped flow CO2 hydration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 12(Homo sapiens (Human))
Universita` Degli Studi Di Firenze

Curated by ChEMBL
LigandPNGBDBM50334349(4-(3-(3-nitrophenyl)ureido)benzenesulfonamide | 4-...)
Affinity DataKi:  5.70nMAssay Description:Inhibition of human CA12 by stopped-flow CO2 hydrase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase(Mycobacterium tuberculosis)
Universit£

Curated by ChEMBL
LigandPNGBDBM50334349(4-(3-(3-nitrophenyl)ureido)benzenesulfonamide | 4-...)
Affinity DataKi:  6.5nMAssay Description:Inhibition of Mycobacterium tuberculosis recombinant beta-carbonic anhydrase Rv3273 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))
Universit£

Curated by ChEMBL
LigandPNGBDBM50334349(4-(3-(3-nitrophenyl)ureido)benzenesulfonamide | 4-...)
Affinity DataKi:  15nMAssay Description:Inhibition of human CA2 by stopped-flow CO2 hydrase assayMore data for this Ligand-Target Pair
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50334349(4-(3-(3-nitrophenyl)ureido)benzenesulfonamide | 4-...)
Affinity DataKi:  15nMAssay Description:Inhibition of human cytosolic carbonic anhydrase 2 preincubated for 15 min by CO2 hydration assayMore data for this Ligand-Target Pair
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50334349(4-(3-(3-nitrophenyl)ureido)benzenesulfonamide | 4-...)
Affinity DataKi:  15nMAssay Description:Inhibition of human carbonic anhydrase 2 for 15 mins by stopped flow CO2 hydration assayMore data for this Ligand-Target Pair
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50334349(4-(3-(3-nitrophenyl)ureido)benzenesulfonamide | 4-...)
Affinity DataKi:  15nMAssay Description:Inhibition of human recombinant carbonic anhydrase 2 preincubated for 15 mins by stopped-flow CO2 hydrase assayMore data for this Ligand-Target Pair
TargetCarbonic anhydrase 1(Homo sapiens (Human))
University Of Florida College Of Medicine

Curated by ChEMBL
LigandPNGBDBM50334349(4-(3-(3-nitrophenyl)ureido)benzenesulfonamide | 4-...)
Affinity DataKi:  23nMAssay Description:Inhibition of human carbonic anhydrase 1 for 15 mins by stopped flow CO2 hydration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
University Of Florida College Of Medicine

Curated by ChEMBL
LigandPNGBDBM50334349(4-(3-(3-nitrophenyl)ureido)benzenesulfonamide | 4-...)
Affinity DataKi:  23nMAssay Description:Inhibition of human cytosolic carbonic anhydrase 1 preincubated for 15 min by CO2 hydration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
University Of Florida College Of Medicine

Curated by ChEMBL
LigandPNGBDBM50334349(4-(3-(3-nitrophenyl)ureido)benzenesulfonamide | 4-...)
Affinity DataKi:  23nMAssay Description:Inhibition of human CA1 by stopped-flow CO2 hydrase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-carbonic anhydrase 1(Mycobacterium tuberculosis)
Universit£

Curated by ChEMBL
LigandPNGBDBM50334349(4-(3-(3-nitrophenyl)ureido)benzenesulfonamide | 4-...)
Affinity DataKi:  67nMAssay Description:Inhibition of Mycobacterium tuberculosis recombinant beta-carbonic anhydrase Rv1284 preincubated for 15 mins by stopped-flow CO2 hydrase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 5B, mitochondrial(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50334349(4-(3-(3-nitrophenyl)ureido)benzenesulfonamide | 4-...)
Affinity DataKi:  138nMAssay Description:Inhibition of human CA5B by stopped-flow CO2 hydrase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 5A, mitochondrial(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50334349(4-(3-(3-nitrophenyl)ureido)benzenesulfonamide | 4-...)
Affinity DataKi:  146nMAssay Description:Inhibition of human CA5A by stopped-flow CO2 hydrase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed