BDBM50334363 4-(3-(4-butylphenyl)ureido)benzenesulfonamide::4-({[(4'-Butylphenyl)amino]carbonyl}amino)benzenesulfonamide::CHEMBL1643297

SMILES CCCCc1ccc(NC(=O)Nc2ccc(cc2)S(N)(=O)=O)cc1

InChI Key InChIKey=KCFQSKKKOAPUSR-UHFFFAOYSA-N

Data  7 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 7 hits for monomerid = 50334363   

TargetCarbonic anhydrase 12(Homo sapiens (Human))
Universita` Degli Studi Di Firenze

Curated by ChEMBL
LigandPNGBDBM50334363(4-(3-(4-butylphenyl)ureido)benzenesulfonamide | 4-...)
Affinity DataKi:  29nMAssay 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(Mycobacterium tuberculosis)
Universit£

Curated by ChEMBL
LigandPNGBDBM50334363(4-(3-(4-butylphenyl)ureido)benzenesulfonamide | 4-...)
Affinity DataKi:  64nMAssay 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 9(Homo sapiens (Human))
Universita` Degli Studi Di Firenze

Curated by ChEMBL
LigandPNGBDBM50334363(4-(3-(4-butylphenyl)ureido)benzenesulfonamide | 4-...)
Affinity DataKi:  376nMAssay 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
LigandPNGBDBM50334363(4-(3-(4-butylphenyl)ureido)benzenesulfonamide | 4-...)
Affinity DataKi:  2.49E+3nMAssay 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
LigandPNGBDBM50334363(4-(3-(4-butylphenyl)ureido)benzenesulfonamide | 4-...)
Affinity DataKi:  2.49E+3nMAssay 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
TargetBeta-carbonic anhydrase 1(Mycobacterium tuberculosis)
Universit£

Curated by ChEMBL
LigandPNGBDBM50334363(4-(3-(4-butylphenyl)ureido)benzenesulfonamide | 4-...)
Affinity DataKi:  4.76E+3nMAssay 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 1(Homo sapiens (Human))
Universita` Degli Studi Di Firenze

Curated by ChEMBL
LigandPNGBDBM50334363(4-(3-(4-butylphenyl)ureido)benzenesulfonamide | 4-...)
Affinity DataKi:  5.53E+3nMAssay 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