BDBM50025093 4-Chloro-benzenesulfonamide::CHEMBL804::P-Chlorobenzenesulfonamide::p-Halide-sulfanilamide derivative, 2

SMILES NS(=O)(=O)c1ccc(Cl)cc1

InChI Key InChIKey=HHHDJHHNEURCNV-UHFFFAOYSA-N

Data  5 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 5 hits for monomerid = 50025093   

LigandPNGBDBM50025093(4-Chloro-benzenesulfonamide | CHEMBL804 | P-Chloro...)
Affinity DataKi:  0.300nMAssay Description:Compound was evaluated for the inhibition of Carbonic anhydraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Bos taurus)
The University Of Tokushima Graduate School

Curated by ChEMBL
LigandPNGBDBM50025093(4-Chloro-benzenesulfonamide | CHEMBL804 | P-Chloro...)
Affinity DataKi:  14nMAssay Description:Binding affinity to bovine carbonic anhydrase 2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Bos taurus)
The University Of Tokushima Graduate School

Curated by ChEMBL
LigandPNGBDBM50025093(4-Chloro-benzenesulfonamide | CHEMBL804 | P-Chloro...)
Affinity DataKi:  14nMAssay Description:Binding affinity to bovine carbonic anhydrase 2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Universita Degli Studi Di Firenze

LigandPNGBDBM50025093(4-Chloro-benzenesulfonamide | CHEMBL804 | P-Chloro...)
Affinity DataKi:  17.5nM ΔG°:  -10.6kcal/molepH: 7.4 T: 2°CAssay Description:Carbonic anhydrase (CA) inhibition against hCA II and V11 with synthesized compounds 2-8.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 7(Homo sapiens (Human))
Universita Degli Studi Di Firenze

LigandPNGBDBM50025093(4-Chloro-benzenesulfonamide | CHEMBL804 | P-Chloro...)
Affinity DataKi:  53nM ΔG°:  -9.92kcal/molepH: 7.4 T: 2°CAssay Description:Carbonic anhydrase (CA) inhibition against hCA II and V11 with synthesized compounds 2-8.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed