BDBM10875 5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide::CHEMBL360356::Chlorzolamide, CHL::JMC522226 Compound 19::JMC523116 Compound 19::aromatic/heteroaromatic sulfonamide 20

SMILES NS(=O)(=O)c1nnc(s1)-c1ccccc1Cl

InChI Key InChIKey=PZVGOWIIHCUHAO-UHFFFAOYSA-N

Data  46 KI

PDB links: 3 PDB IDs match this monomer.

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 46 hits for monomerid = 10875   

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

LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  1nMAssay Description:Inhibition assay using carbonic anhydrases.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
University Of Florida

LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  1.10nMAssay Description:Inhibition assay using carbonic anhydrases.More data for this Ligand-Target Pair
TargetCarbonic anhydrase 2(Homo sapiens (Human))
University Of Florida

LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  2nMAssay Description:Inhibition assay using carbonic anhydrases.More data for this Ligand-Target Pair
TargetCarbonic anhydrase, alpha family(Thiomicrospira crunogena (strain XCL-2))
Universit£

Curated by ChEMBL
LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  2.5nMAssay Description:Inhibition of recombinant Thiomicrospira crunogena XCL-2 carbonic anhydrase by stopped flow CO2 hydrase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 7(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  5.40nMAssay Description:Ki value against human carbonic anhydrase VIIMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
University Of Florida

LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  12nMAssay Description:An Applied Photophysics stopped-flow instrument has been used for assaying the CA-catalyzed CO2 hydration activity. Phenol red has been used as indic...More data for this Ligand-Target Pair
TargetCarbonic anhydrase 2(Homo sapiens (Human))
University Of Florida

LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  12nMAssay Description:Inhibition of human carbonic anhydrase 2 preincubated for 15 mins measured for 10 to 100 sec by stopped-flow methodMore data for this Ligand-Target Pair
TargetCarbonic anhydrase 2(Homo sapiens (Human))
University Of Florida

LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  12nMAssay Description:An Applied Photophysics stopped-flow instrument has been used for assaying the CA-catalyzed CO2 hydration activity. Phenol red has been used as indic...More data for this Ligand-Target Pair
TargetCarbonic anhydrase 2(Homo sapiens (Human))
University Of Florida

LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  12nMAssay Description:Inhibition of human recombinant CA2 by stopped-flow CO2 hydrase assayMore data for this Ligand-Target Pair
TargetCarbonic anhydrase 2(Homo sapiens (Human))
University Of Florida

LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  12nMAssay Description:Inhibition of human recombinant CA2 by stopped-flow hydration assayMore data for this Ligand-Target Pair
TargetCarbonic anhydrase 2(Homo sapiens (Human))
University Of Florida

LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  12nMAssay Description:Inhibition of human recombinant cytosolic isozyme CA II by stopped-flow CO2 hydrase methodMore data for this Ligand-Target Pair
TargetCarbonic anhydrase 2(Homo sapiens (Human))
University Of Florida

LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  12nMAssay Description:Ki value against human carbonic anhydrase IIMore data for this Ligand-Target Pair
TargetCarbonic anhydrase 2(Homo sapiens (Human))
University Of Florida

LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  12nMAssay Description:Inhibition of human recombinant CA2More data for this Ligand-Target Pair
TargetCarbonic anhydrase 2(Homo sapiens (Human))
University Of Florida

LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  12nMAssay Description:Ki value against human carbonic anhydrase II (hCA II)More data for this Ligand-Target Pair
TargetCarbonic anhydrase 2(Homo sapiens (Human))
University Of Florida

LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  12nMAssay Description:Inhibition of human recombinant carbonic anhydrase 2 after 15 mins by stopped flow CO2 hydration assayMore data for this Ligand-Target Pair
TargetCarbonic anhydrase 2(Homo sapiens (Human))
University Of Florida

LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  12nMpH: 7.5Assay Description:Inhibition of human recombinant carbonic anhydrase 2 at pH 7.5 by stopped flow CO2 hydration assayMore data for this Ligand-Target Pair
TargetCarbonic anhydrase 2(Homo sapiens (Human))
University Of Florida

LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  12nMpH: 7.5Assay Description:Inhibition of human carbonic anhydrase II by spectrophotometry at pH 7.5More data for this Ligand-Target Pair
TargetCarbonic anhydrase 2(Homo sapiens (Human))
University Of Florida

LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  12nMAssay Description:Inhibition of recombinant human carbonic anhydrase-2 by stopped flow CO2 hydrase assayMore data for this Ligand-Target Pair
TargetCarbonic anhydrase 9(Homo sapiens (Human))
University Of Florida

LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  30nMAssay Description:Inhibition of catalytic domain of human recombinant CA IXMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 5B, mitochondrial(Homo sapiens (Human))
Kochi Medical School

LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  30nMAssay Description:An Applied Photophysics stopped-flow instrument has been used for assaying the CA-catalyzed CO2 hydration activity. Phenol red has been used as indic...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 12(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  36nMAssay Description:Ki value against human carbonic anhydrase XII (hCA XII)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 5A, mitochondrial(Homo sapiens (Human))
Kochi Medical School

LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  43nMAssay Description:An Applied Photophysics stopped-flow instrument has been used for assaying the CA-catalyzed CO2 hydration activity. Phenol red has been used as indic...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 15 [19-324](Mus musculus (mouse))
University Of Tampere

LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  60nM ΔG°:  -9.68kcal/molepH: 7.5 T: 2°CAssay Description:An Applied Photophysics stopped-flow instrument has been used for assaying the CA-catalyzed CO2 hydration activity. Phenol red has been used as indic...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase(Sulfurihydrogenibium sp. (strain YO3AOP1))
Universit£

Curated by ChEMBL
LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  70nMAssay Description:Inhibition of recombinant Sulfurihydrogenibium yellowstonense YO3AOP1 carbonic anhydrase by stopped flow CO2 hydrase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase(Helicobacter pylori (strain G27))
Kochi Medical School

Curated by ChEMBL
LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  84nMAssay Description:Inhibition of Helicobacter pylori recombinant CAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCARBONIC ANHYDRASE(Helicobacter pylori J99)
Kochi Medical School

LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  105nMAssay Description:An Applied Photophysics stopped-flow instrument has been used for assaying the CA-catalyzed CO2 hydration activity. Phenol red has been used as indic...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 6(Homo sapiens (Human))
University Of Tampere

LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  114nMAssay Description:An Applied Photophysics stopped-flow instrument has been used for assaying the CA-catalyzed CO2 hydration activity. Phenol red has been used as indic...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 6(Homo sapiens (Human))
University Of Tampere

LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  114nMAssay Description:Inhibition of full length human recombinant CA VIMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase(Cryptococcus neoformans var. grubii (Filobasidiell...)
Universite Degli Studi Di Firenze

LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  379nMAssay Description:An Applied Photophysics stopped-flow instrument has been used for assaying the CA-catalyzed CO2 hydration activity. Phenol red has been used as indic...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase(Saccharomyces cerevisiae)
Balikesir University

Curated by ChEMBL
LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  565nMAssay Description:Inhibition of Saccharomyces cerevisiae recombinant CA expressed in Escherichia coli by stopped-flow CO2 hydrase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  690nMAssay Description:Inhibition of recombinant human carbonic anhydrase-1 by stopped flow CO2 hydrase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  690nMAssay Description:An Applied Photophysics stopped-flow instrument has been used for assaying the CA-catalyzed CO2 hydration activity. Phenol red has been used as indic...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  690nMAssay Description:Inhibition of human recombinant CA1 by stopped-flow CO2 hydrase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  690nMAssay Description:Ki value against human carbonic anhydrase IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  690nMAssay Description:Inhibition of human recombinant CA1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  690nMAssay Description:Ki value against human carbonic anhydrase I (hCA I)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  690nMAssay Description:Inhibition of human recombinant carbonic anhydrase 1 after 15 mins by stopped flow CO2 hydration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  690nMpH: 7.5Assay Description:Inhibition of human recombinant carbonic anhydrase 1 at pH 7.5 by stopped flow CO2 hydration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  690nMAssay Description:Inhibition of human recombinant cytosolic isozyme CA I by stopped-flow CO2 hydrase methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  690nMpH: 7.5Assay Description:Inhibition of human carbonic anhydrase I by spectrophotometry at pH 7.5More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase(Astrosclera willeyana)
Slovak Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  792nMAssay Description:Inhibition of GST-tagged astrosclera willeyana Astrosclerin-3 expressed in Escherichia coli after 15 mins preincubation by stopped flow CO2 hydration...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase(Candida albicans (Yeast))
Universite Degli Studi Di Firenze

LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  1.29E+3nM ΔG°:  -7.89kcal/molepH: 8.3 T: 2°CAssay Description:An Applied Photophysics stopped-flow instrument has been used for assaying the CA-catalyzed CO2 hydration activity. Phenol red has been used as indic...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-carbonic anhydrase 1(Mycobacterium tuberculosis)
Kochi Medical School

LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  7.48E+3nM ΔG°:  -6.87kcal/molepH: 8.3 T: 2°CAssay Description:An Applied Photophysics stopped-flow instrument has been used for assaying the CA-catalyzed CO2 hydration activity. Phenol red has been used as indic...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase(Mycobacterium tuberculosis)
Kochi Medical School

LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  7.60E+3nM ΔG°:  -6.86kcal/molepH: 8.3 T: 2°CAssay Description:An Applied Photophysics stopped-flow instrument has been used for assaying the CA-catalyzed CO2 hydration activity. Phenol red has been used as indic...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 3(Homo sapiens (Human))
Kochi Medical School

Curated by ChEMBL
LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  1.46E+4nMAssay Description:Inhibition of human recombinant CA 3 assessed as CO2 hydration by stopped flow kinetic assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Mycobacterium tuberculosis)
Universit£

Curated by ChEMBL
LigandPNGBDBM10875(5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide...)
Affinity DataKi:  4.52E+4nMAssay Description:Inhibition of full length Mycobacterium tuberculosis H37Rv recombinant carbonic anhydrase 2 encoded by RV3588c by stopped flow CO2 hydration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed