BDBM50228326 CHEMBL1795055::CHEMBL285436::{(2-{Carboxymethyl-[(4-sulfamoyl-benzylcarbamoyl)-methyl]-amino}-ethyl)-[(4-sulfamoyl-benzylcarbamoyl)-methyl]-amino}-acetic acid::{(2-{Carboxymethyl-[(4-sulfamoyl-benzylcarbamoyl)-methyl]-amino}-ethyl)-[(4-sulfamoyl-benzylcarbamoyl)-methyl]-amino}-acetic acid; compound with Zn complex

SMILES NS(=O)(=O)c1ccc(CNC(=O)CN(CCN(CC(O)=O)CC(=O)NCc2ccc(cc2)S(N)(=O)=O)CC(O)=O)cc1

InChI Key InChIKey=GMDCWQKESXVLDQ-UHFFFAOYSA-N

Data  10 KI

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 10 hits for monomerid = 50228326   

TargetCarbonic anhydrase 2(Homo sapiens (Human))
Ecole Nationale Sup£Rieure De Chimie De Montpellier

Curated by ChEMBL
LigandPNGBDBM50228326(CHEMBL1795055 | CHEMBL285436 | {(2-{Carboxymethyl-...)
Affinity DataKi:  0.890nMAssay Description:Inhibition of human recombinant CA2 by CO2 hydration stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 12(Homo sapiens (Human))
Ecole Nationale Sup£Rieure De Chimie De Montpellier

Curated by ChEMBL
LigandPNGBDBM50228326(CHEMBL1795055 | CHEMBL285436 | {(2-{Carboxymethyl-...)
Affinity DataKi:  3nMAssay Description:Inhibition of human recombinant CA12 by CO2 hydration stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Ecole Nationale Sup£Rieure De Chimie De Montpellier

Curated by ChEMBL
LigandPNGBDBM50228326(CHEMBL1795055 | CHEMBL285436 | {(2-{Carboxymethyl-...)
Affinity DataKi:  6nMAssay Description:Inhibitory activity against Human carbonic anhydrase IIMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 9(Homo sapiens (Human))
Ecole Nationale Sup£Rieure De Chimie De Montpellier

Curated by ChEMBL
LigandPNGBDBM50228326(CHEMBL1795055 | CHEMBL285436 | {(2-{Carboxymethyl-...)
Affinity DataKi:  7.30nMAssay Description:Inhibition of human recombinant CA9 by CO2 hydration stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 4(Bos taurus (bovine))
Universit£

Curated by ChEMBL
LigandPNGBDBM50228326(CHEMBL1795055 | CHEMBL285436 | {(2-{Carboxymethyl-...)
Affinity DataKi:  10nMAssay Description:Inhibitory activity against bovine carbonic anhydrase IVMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Ecole Nationale Sup£Rieure De Chimie De Montpellier

Curated by ChEMBL
LigandPNGBDBM50228326(CHEMBL1795055 | CHEMBL285436 | {(2-{Carboxymethyl-...)
Affinity DataKi:  36nMAssay Description:Inhibitory activity against Human carbonic anhydrase IIMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50228326(CHEMBL1795055 | CHEMBL285436 | {(2-{Carboxymethyl-...)
Affinity DataKi:  45nMAssay Description:Inhibitory activity against Human carbonic anhydrase IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 4(Bos taurus (bovine))
Universit£

Curated by ChEMBL
LigandPNGBDBM50228326(CHEMBL1795055 | CHEMBL285436 | {(2-{Carboxymethyl-...)
Affinity DataKi:  62nMAssay Description:Inhibitory activity against bovine carbonic anhydrase IVMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50228326(CHEMBL1795055 | CHEMBL285436 | {(2-{Carboxymethyl-...)
Affinity DataKi:  438nMAssay Description:Inhibition of human recombinant CA1 by CO2 hydration stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50228326(CHEMBL1795055 | CHEMBL285436 | {(2-{Carboxymethyl-...)
Affinity DataKi:  510nMAssay Description:Inhibitory activity against Human carbonic anhydrase IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed