BDBM50334346 4-(3-(2-cyanophenyl)ureido)benzenesulfonamide::4-{([(2'-Cyanophenyl)amino]carbonyl)amino}benzenesulfonamide::CA IX inhibitor, (C)3::CHEMBL1643301

SMILES NS(=O)(=O)c1ccc(NC(=O)Nc2ccccc2C#N)cc1

InChI Key InChIKey=HOUIRAFTHIMUSN-UHFFFAOYSA-N

Data  8 KI

  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 8 hits for monomerid = 50334346   

TargetCarbonic anhydrase 9(Homo sapiens (Human))
Bc Cancer Agency

LigandPNGBDBM50334346(4-(3-(2-cyanophenyl)ureido)benzenesulfonamide | 4-...)
Affinity DataKi:  0.300nMAssay 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))
Bc Cancer Agency

LigandPNGBDBM50334346(4-(3-(2-cyanophenyl)ureido)benzenesulfonamide | 4-...)
Affinity DataKi:  0.300nMAssay 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 2(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50334346(4-(3-(2-cyanophenyl)ureido)benzenesulfonamide | 4-...)
Affinity DataKi:  2.40nMAssay Description:Inhibition of human recombinant 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))
Universit£

Curated by ChEMBL
LigandPNGBDBM50334346(4-(3-(2-cyanophenyl)ureido)benzenesulfonamide | 4-...)
Affinity DataKi:  2.40nMAssay Description:Inhibition of human cytosolic carbonic anhydrase 2 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
LigandPNGBDBM50334346(4-(3-(2-cyanophenyl)ureido)benzenesulfonamide | 4-...)
Affinity DataKi:  4.60nMAssay 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 1(Homo sapiens (Human))
Universita` Degli Studi Di Firenze

Curated by ChEMBL
LigandPNGBDBM50334346(4-(3-(2-cyanophenyl)ureido)benzenesulfonamide | 4-...)
Affinity DataKi:  11nMAssay 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(Mycobacterium tuberculosis)
Universit£

Curated by ChEMBL
LigandPNGBDBM50334346(4-(3-(2-cyanophenyl)ureido)benzenesulfonamide | 4-...)
Affinity DataKi:  463nMAssay 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
TargetBeta-carbonic anhydrase 1(Mycobacterium tuberculosis)
Universit£

Curated by ChEMBL
LigandPNGBDBM50334346(4-(3-(2-cyanophenyl)ureido)benzenesulfonamide | 4-...)
Affinity DataKi:  534nMAssay 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