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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
(change energy unit to
kcal/mol
)
Found
262
hits in this display
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
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Affinity Data
Ki: 0.00300nM
Assay Description:
Inhibition of human CA2
More data for this Ligand-Target Pair
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3D Structure (crystal)
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Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 23nM
pH: 7.4
Assay Description:
CA activity was assayed by following the change in absorbance at 348 nm of 4-nitrophenylacetate (NPA) to 4-nitrophenylate ion over a period of 3 min ...
More data for this Ligand-Target Pair
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Target
Carbonic anhydrase 13
(Mus musculus (mouse))
University Of Tampere
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 32nM
Assay Description:
Inhibitory activity against murine carbonic anhydrase XIII (mCA XIII) by using CO2 hydrase assay method
More data for this Ligand-Target Pair
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Target
Carbonic anhydrase 13
(Mus musculus (mouse))
University Of Tampere
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 32nM
Assay Description:
Ki value against murine carbonic anhydrase XIII
More data for this Ligand-Target Pair
Target Info
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Target
Carbonic anhydrase 13
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 32nM
Assay Description:
Inhibition of human recombinant CA13 by stopped flow CO2 hydrase assay
More data for this Ligand-Target Pair
Target Info
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Target
Carbonic anhydrase 13
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 35nM
Assay Description:
Inhibition of human CA13 preincubated for 15 mins by stopped-flow CO2 hydration method
More data for this Ligand-Target Pair
Target Info
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Target
Carbonic anhydrase 12
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 37nM
Assay Description:
Inhibitory constant against catalytic domain of human carbonic anhydrase XII
More data for this Ligand-Target Pair
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Copy BDB DOI
Target
Carbonic anhydrase 12
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 37nM
Assay Description:
Inhibition of human recombinant CA12 by CO2 hydration stopped flow assay
More data for this Ligand-Target Pair
Target Info
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Copy BDB DOI
Target
Carbonic anhydrase 12
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 37nM
Assay Description:
Inhibition of human catalytic domain of carbonic anhydrase 12 preincubated for 15 mins by CO2 hydration stopped-flow assay
More data for this Ligand-Target Pair
Target Info
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Details
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PubMed
Copy BDB DOI
Target
Carbonic anhydrase 12
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 37nM
Assay Description:
Inhibitory activity against catalytic domain of human carbonic anhydrase XII
More data for this Ligand-Target Pair
Target Info
PDB
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Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
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Ligand Info
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ChEBI
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MCE
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 12
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 37nM
Assay Description:
Inhibition of human carbonic anhydrase 12 catalytic domain preincubated for 15 mins by stopped flow CO2 hydration assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
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antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
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MCE
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PC sid
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 12
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 37nM
Assay Description:
Inhibition of human carbonic anhydrase 12-catalyzed CO2 hydration activity by stopped flow assay
More data for this Ligand-Target Pair
Target Info
PDB
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KEGG
UniProtKB/SwissProt
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Ligand Info
Purchase
ChEBI
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MCE
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 12
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 37nM
Assay Description:
Inhibition of human recombinant catalytic domain of carbonic anhydrase 12 preincubated for 15 mins by stopped-flow CO2 hydration assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
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GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
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MCE
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 12
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 37nM
Assay Description:
Inhibitiory activity against human Carbonic anhydrase XII (hCA XII)
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
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antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
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MCE
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Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 12
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 37nM
Assay Description:
Inhibition of human recombinant transmembrane tumor associated carbonic anhydrase-12 incubated for 15 mins prior to testing by stopped-flow CO2 hydra...
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
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DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
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MCE
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 12
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 37nM
Assay Description:
Inhibition of human CA12 preincubated for 15 mins by stopped-flow CO2 hydration method
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
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PC sid
PDB
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 12
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 37nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase-12 preincubated for 10 mins by stopped-flow CO2 hydration assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
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MCE
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PDB
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 12
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 37nM
Assay Description:
Inhibition of human recombinant CA12 by stopped flow CO2 hydrase assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
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antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
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PubMed
Copy BDB DOI
Target
Carbonic anhydrase 7
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 70nM
Assay Description:
Ki value against human carbonic anhydrase VII
More data for this Ligand-Target Pair
Target Info
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Details
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PubMed
Copy BDB DOI
Target
Carbonic anhydrase 7
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 70nM
Assay Description:
Inhibition of human CA7 preincubated for 15 mins by stopped-flow CO2 hydration method
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
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ChEBI
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Copy BDB DOI
Target
Carbonic anhydrase 7
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 70nM
Assay Description:
Inhibition of human recombinant CA7 by stopped flow CO2 hydrase assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
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Target
Delta carbonic anhydrase
(Thalassiosira weissflogii)
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 181nM
Assay Description:
Inhibition of Thalassiosira weissflogii delta carbonic anhydrase preincubated for 15 mins by stopped flow CO2 hydration assay
More data for this Ligand-Target Pair
Target Info
UniProtKB/TrEMBL
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Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 238nM
Assay Description:
Inhibition of catalytic domain of human recombinant CA IX
More data for this Ligand-Target Pair
Target Info
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MMDB
NCI pathway
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KEGG
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Copy BDB DOI
Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 238nM
Assay Description:
Inhibition of human CA9 preincubated for 15 mins by stopped-flow CO2 hydration method
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
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Copy BDB DOI
Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 238nM
Assay Description:
Inhibition of human recombinant CA9 by stopped flow CO2 hydrase assay
More data for this Ligand-Target Pair
Target Info
PDB
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Reactome pathway
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Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human carbonic anhydrase 2 preincubated for 15 mins measured for 10 to 100 sec by stopped-flow method
More data for this Ligand-Target Pair
Target Info
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3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human carbonic anhydrase 2 assessed as reduction in CO2 hydration preincubated for 15 mins followed by CO2 addition measured for 10 to ...
More data for this Ligand-Target Pair
Target Info
PDB
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3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase-2 preincubated for 10 mins by stopped-flow CO2 hydration assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
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ChEBI
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PDB
3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human carbonic anhydrase-2 assessed as reduction in CO2 hydration preincubated for 15 mins followed by CO2 addition measured for 10 to ...
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
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antibodypedia
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ChEBI
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PDB
3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human CA2 cytosolic isoform preincubated for 15 mins by stopped-flow CO2 hydration method
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
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3D Structure (crystal)
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Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human cytosolic carbonic anhydrase 2 preincubated for 15 mins by stop flow CO2 hydrase assay
More data for this Ligand-Target Pair
Target Info
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PDB
3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human cytosolic carbonic anhydrase 2 preincubated for 15 mins by stop flow CO2 hydrase assay
More data for this Ligand-Target Pair
Target Info
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PDB
3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
pH: 7.5
Assay Description:
Inhibition of human carbonic anhydrase II by spectrophotometry at pH 7.5
More data for this Ligand-Target Pair
Target Info
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PDB
3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human full length cytosolic isoform of carbonic anhydrase 2 preincubated for 15 mins by CO2 hydration stopped-flow assay
More data for this Ligand-Target Pair
Target Info
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PDB
3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
pH: 7.5
Assay Description:
Inhibition of human recombinant carbonic anhydrase 2 at pH 7.5 by stopped flow CO2 hydration assay
More data for this Ligand-Target Pair
Target Info
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PDB
3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human carbonic anhydrase 2-catalyzed CO2 hydration activity by stopped flow assay
More data for this Ligand-Target Pair
Target Info
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PDB
3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human recombinant CA2 by stopped-flow CO2 hydrase assay
More data for this Ligand-Target Pair
Target Info
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PDB
3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human recombinant alpha-carbonic anhydrase 2 after 15 mins by stopped flow CO2 hydration assay
More data for this Ligand-Target Pair
Target Info
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PDB
3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human recombinant CA2 by stopped-flow CO2 assay
More data for this Ligand-Target Pair
Target Info
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PDB
3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human recombinant CA2 by stopped-flow hydration assay
More data for this Ligand-Target Pair
Target Info
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PDB
3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human recombinant CA2 by stopped-flow CO2 hydration assay
Checked by Author
More data for this Ligand-Target Pair
Target Info
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PDB
3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 2 preincubated for 15 mins by stopped-flow CO2 hydrase assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
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PDB
3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 2 after 15 mins by CO2 hydration method
More data for this Ligand-Target Pair
Target Info
PDB
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KEGG
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PDB
3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 2 after 15 mins by stopped flow carbondioxide hydrase assay method
More data for this Ligand-Target Pair
Target Info
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PDB
3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of recombinant human carbonic anhydrase 2 preincubated for 15 mins by stopped-flow CO2 hydration assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
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PubMed
PDB
3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human carbonic anhydrase 2 preincubated for 15 mins by CO2 hydrase stopped flow assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
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PDB
3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human carbonic anhydrase 2 incubated for 15 mins by stopped-flow CO2 hydration assay
More data for this Ligand-Target Pair
Target Info
PDB
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KEGG
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PDB
3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human Carbonic anhydrase2 using CO2 as substrate preincubated for 15 mins by stopped-flow CO2 hydration assay
More data for this Ligand-Target Pair
Target Info
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PDB
3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of recombinant human carbonic anhydrase-2 by stopped flow CO2 hydrase assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
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Ligand Info
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PDB
3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase-2 by stopped flow CO2 hydrase assay method
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
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PDB
3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human carbonic anhydrase 2 pre-incubated for 15 mins by stopped-flow CO2 hydration assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
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Ligand Info
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PDB
3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 2 by stopped flow CO2 hydrase assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
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Ligand Info
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ChEBI
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PDB
3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human recombinant Carbonic anhydrase 2 compound preincubated for 15 mins by stopped flow CO2 hydrase assay method
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
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PDB
3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 2 by stopped-flow CO2 hydration assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
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PDB
3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human carbonic anhydrase-2 by stopped-flow CO2 hydration assay
More data for this Ligand-Target Pair
Target Info
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Reactome pathway
KEGG
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3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM ΔG°: -37.8kJ/mole
pH: 7.5 T: 2°C
Assay 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
Target Info
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3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay 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
Target Info
PDB
MMDB
Reactome pathway
KEGG
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DrugBank
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PDB
3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 2 after 15 mins by stopped flow CO2 hydration assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
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Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human cloned carbonic anhydrase 2 preincubated for 15 mins by stopped flow CO2 hydration assay
More data for this Ligand-Target Pair
Target Info
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3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human wild type carbonic anhydrase 2 expressed in Escherichia coli after 15 mins preincubation by stopped flow CO2 hydration assay
More data for this Ligand-Target Pair
Target Info
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3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human recombinant CA2
More data for this Ligand-Target Pair
Target Info
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3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Ki value against human carbonic anhydrase II
More data for this Ligand-Target Pair
Target Info
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3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human recombinant CA2 by CO2 hydration stopped flow assay
More data for this Ligand-Target Pair
Target Info
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3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human recombinant cytosolic isozyme CA II by stopped-flow CO2 hydrase method
More data for this Ligand-Target Pair
Target Info
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3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 2 by stopped flow CO2 hydration assay
More data for this Ligand-Target Pair
Target Info
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PDB
3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 2 preincubated for 15 mins by CO2 hydration stopped-flow assay
More data for this Ligand-Target Pair
Target Info
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PDB
3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 240nM
Assay Description:
Inhibition of human recombinant CA2 by stopped flow CO2 hydrase assay
More data for this Ligand-Target Pair
Target Info
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3D Structure (crystal)
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Target
Carbonic anhydrase
(Methanosarcina thermophila)
Pennsylvania State University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 250nM
Assay Description:
Inhibitory activity against alpha carbonic anhydrase (Zn-Cam) from Methanosarcina thermophila
More data for this Ligand-Target Pair
Target Info
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Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 294nM
Assay Description:
Inhibition of human carbonic anhydrase 9-catalyzed CO2 hydration activity by stopped flow assay
More data for this Ligand-Target Pair
Target Info
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Copy BDB DOI
Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 294nM
Assay Description:
Inhibition of human recombinant CA9 by CO2 hydration stopped flow assay
More data for this Ligand-Target Pair
Target Info
PDB
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Copy BDB DOI
Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 294nM
Assay Description:
Inhibitory constant against human Carbonic anhydrase IX
More data for this Ligand-Target Pair
Target Info
PDB
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KEGG
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Copy BDB DOI
Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 294nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase-9 preincubated for 10 mins by stopped-flow CO2 hydration assay
More data for this Ligand-Target Pair
Target Info
PDB
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Copy BDB DOI
Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 294nM
Assay Description:
Inhibitiory activity against human Carbonic anhydrase IX (hCA IX)
More data for this Ligand-Target Pair
Target Info
PDB
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Copy BDB DOI
Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 294nM
Assay Description:
Inhibitory activity against human carbonic anhydrase IX expressed in Escherichia coli BL21
More data for this Ligand-Target Pair
Target Info
PDB
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Copy BDB DOI
Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 294nM
Assay Description:
Inhibitory potency against catalytic domain of human Carbonic anhydrase IX expressed in Escherichia coli strain BL21
More data for this Ligand-Target Pair
Target Info
PDB
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Copy BDB DOI
Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 294nM
Assay Description:
Inhibitory constant against catalytic domain of human carbonic anhydrase IX
More data for this Ligand-Target Pair
Target Info
PDB
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KEGG
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Copy BDB DOI
Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 294nM
Assay Description:
Inhibitory activity against human carbonic anhydrase IX (hCA IX) by using CO2 hydrase assay method
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
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Copy BDB DOI
Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 294nM
Assay Description:
Inhibitory activity against human tumor-associated transmembrane carbonic anhydrase IX.
More data for this Ligand-Target Pair
Target Info
PDB
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KEGG
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Copy BDB DOI
Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 294nM
Assay Description:
Inhibitory activity against human cloned carbonic anhydrase isozyme IX, by CO2 hydrase assay method.
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
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KEGG
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Copy BDB DOI
Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 294nM
Assay Description:
Inhibition of human catalytic domain of carbonic anhydrase 9 preincubated for 15 mins by CO2 hydration stopped-flow assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
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Copy BDB DOI
Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 294nM
Assay Description:
Inhibition of human carbonic anhydrase 9 catalytic domain preincubated for 15 mins by stopped flow CO2 hydration assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
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Ligand Info
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ChEBI
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Copy BDB DOI
Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 294nM
Assay Description:
Inhibition of human recombinant transmembrane tumor associated carbonic anhydrase-9 incubated for 15 mins prior to testing by stopped-flow CO2 hydras...
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
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KEGG
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Copy BDB DOI
Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 294nM
Assay 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
Target Info
PDB
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Copy BDB DOI
Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 294nM
Assay Description:
Inhibition constant against human recombinant carbonic anhydrase IX catalytic domain
More data for this Ligand-Target Pair
Target Info
PDB
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Copy BDB DOI
Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 294nM
Assay Description:
Inhibition of human recombinant catalytic domain of carbonic anhydrase 9 preincubated for 15 mins by stopped-flow CO2 hydration assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
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Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 300nM
Assay Description:
Inhibition of human carbonic anhydrase II (hCA II)
More data for this Ligand-Target Pair
Target Info
PDB
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Reactome pathway
KEGG
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Ligand Info
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ChEBI
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PDB
3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 300nM
Assay Description:
Inhibitiory activity against human Carbonic anhydrase II (hCA II)
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
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GoogleScholar
Ligand Info
Purchase
ChEBI
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Target
Carbonic anhydrase
(Stylophora pistillata)
Centre Scientifique De Monaco
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 300nM
Assay Description:
Inhibition of Stylophora pistillata carbonic anhydrase 2 by stopped-flow CO2 hydration assay
Checked by Author
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Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 300nM
Assay Description:
Inhibition of human carbonic anhydrase II
More data for this Ligand-Target Pair
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3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 300nM
Assay Description:
Inhibition of human carbonic anhydrase II
More data for this Ligand-Target Pair
Target Info
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3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 300nM
Assay Description:
Inhibition of cloned isozyme, human carbonic anhydrase II
More data for this Ligand-Target Pair
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3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 300nM
Assay Description:
Inhibitory activity against human carbonic anhydrase II (hCA II) by using esterase assay method
More data for this Ligand-Target Pair
Target Info
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3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 300nM
Assay Description:
Inhibitory activity against human recombinant carbonic anhydrase II
More data for this Ligand-Target Pair
Target Info
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3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 300nM
Assay Description:
Inhibitory activity against human recombinant carbonic anhydrase II (CA2)
More data for this Ligand-Target Pair
Target Info
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3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 300nM
Assay Description:
Inhibitory activity against Human carbonic anhydrase II
More data for this Ligand-Target Pair
Target Info
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3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 300nM
Assay Description:
Inhibitory activity against human carbonic anhydrase II
More data for this Ligand-Target Pair
Target Info
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3D Structure (crystal)
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Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 300nM
Assay Description:
Inhibitory potency against human cloned Carbonic anhydrase II expressed in Escherichia coli strain BL21
More data for this Ligand-Target Pair
Target Info
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3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 300nM
Assay Description:
Inhibitory activity against human carbonic anhydrase II (hCAII)
More data for this Ligand-Target Pair
Target Info
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3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 300nM
Assay Description:
Inhibitory activity against human carbonic anhydrase II expressed in Escherichia coli BL21
More data for this Ligand-Target Pair
Target Info
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3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 300nM
Assay Description:
Inhibition of human carbonic anhydrase II (CAII)
More data for this Ligand-Target Pair
Target Info
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3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 300nM
Assay 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
Target Info
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Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 300nM
Assay Description:
Initial rates of 4-nitrophenyl acetate hydrolysis catalyzed by different CA isozymes were monitored spectrophotometrically at 400 nm. A molar absorpt...
More data for this Ligand-Target Pair
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Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 300nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 2 preincubated for 15 mins by CO2 hydration stopped-flow assay
More data for this Ligand-Target Pair
Target Info
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Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 300nM
Assay Description:
Inhibition of human recombinant cytosolic human carbonic anhydrase-2 incubated for 15 mins prior to testing by stopped-flow CO2 hydrase assay
More data for this Ligand-Target Pair
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3D Structure (crystal)
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Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 300nM
Assay Description:
Inhibition of human carbonic anhydrase 1-catalyzed CO2 hydration preincubated for 10 mins by stopped-flow assay
More data for this Ligand-Target Pair
Target Info
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Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 300nM
Assay Description:
Inhibitory activity against human carbonic anhydrase II (CA2)
More data for this Ligand-Target Pair
Target Info
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Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 300nM
Assay Description:
Inhibitory constant against human Carbonic anhydrase II
More data for this Ligand-Target Pair
Target Info
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Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 300nM
Assay Description:
Inhibition constant against human recombinant carbonic anhydrase II
More data for this Ligand-Target Pair
Target Info
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Copy BDB DOI
Target
Carbonic anhydrase
(Stylophora pistillata)
Centre Scientifique De Monaco
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 364nM
Assay Description:
Inhibition of Stylophora pistillata carbonic anhydrase by stopped-flow CO2 hydration assay
Checked by Author
More data for this Ligand-Target Pair
Target Info
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Copy BDB DOI
Target
Carbonic anhydrase
(Stylophora pistillata)
Centre Scientifique De Monaco
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 364nM
Assay Description:
Inhibition of cloned Stylophora pistillata alpha-CA expressed in human HEK293 cells by stopped-flow CO2 assay
More data for this Ligand-Target Pair
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Target
Carbonic anhydrase
(Helicobacter pylori (strain G27))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
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Affinity Data
Ki: 431nM
Assay Description:
Inhibition of Helicobacter pylori recombinant CA
More data for this Ligand-Target Pair
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Target
CARBONIC ANHYDRASE
(Helicobacter pylori J99)
Kochi Medical School
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 454nM
Assay 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...
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Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 628nM ΔG°: -35.4kJ/mole
pH: 7.4 T: 2°C
Assay Description:
Carbonic anhydrase activity was assayed by following the change in absorbance at 348 nm of 4-nitrophenylacetate (NPA) to 4-nitrophenylate ion over a ...
More data for this Ligand-Target Pair
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Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 628nM
Assay Description:
Inhibition of cytosolic carbonic anhydrase 2 esterase activity isolated from human serum using 4-nitrophenylacetate as substrate measured over 3 mins...
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Target
Carbonic anhydrase, alpha family
(Thiomicrospira crunogena (strain XCL-2))
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
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Affinity Data
Ki: 628nM
Assay Description:
Inhibition of recombinant Thiomicrospira crunogena XCL-2 carbonic anhydrase by stopped flow CO2 hydrase assay
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Target
Carbonic anhydrase
(Sulfurihydrogenibium sp. (strain YO3AOP1))
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
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Affinity Data
Ki: 652nM
Assay Description:
Inhibition of recombinant Sulfurihydrogenibium yellowstonense YO3AOP1 carbonic anhydrase by stopped flow CO2 hydrase assay
More data for this Ligand-Target Pair
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Target
Carbonic anhydrase
(Cryptococcus neoformans var. grubii (Filobasidiell...)
Universite Degli Studi Di Firenze
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 765nM
Assay 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...
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Carbonic anhydrase
(Cryptococcus neoformans var. grubii (Filobasidiell...)
Universite Degli Studi Di Firenze
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 770nM
Assay Description:
Inhibition of Cryptococcus neoformans recombinant Can2 beta-carbonic anhydrase after 15 mins by stopped flow CO2 hydration assay
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Carbonic anhydrase 2
(Bos taurus)
The University Of Tokushima Graduate School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 851nM
Assay Description:
Binding affinity to bovine carbonic anhydrase 2
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Carbonic anhydrase 2
(Bos taurus)
The University Of Tokushima Graduate School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 851nM
Assay Description:
Binding affinity to bovine carbonic anhydrase 2
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Carbonic anhydrase
(Anopheles gambiae)
University Of Tampere And Tampere University Hospital
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 862nM
Assay Description:
Inhibition of Anopheles gambiae carbonic anhydrase pre-incubated for 15 mins by stopped-flow CO2 hydration assay
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Carbonic anhydrase 6
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 941nM
Assay Description:
Inhibition of human CA6 preincubated for 15 mins by stopped-flow CO2 hydration method
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Carbonic anhydrase 6
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 941nM
Assay Description:
Inhibition of full length human recombinant CA VI
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Carbonic anhydrase 6
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 941nM
Assay Description:
Inhibition of human recombinant CA6 by stopped-flow CO2 hydration assay
Checked by Author
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Carbonic anhydrase 6
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 941nM
Assay Description:
Inhibition of human recombinant CA6 by stopped flow CO2 hydrase assay
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Carbonic anhydrase 6
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 941nM
Assay 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...
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Carbonic anhydrase 3
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 988nM
Assay Description:
Inhibition of human recombinant CA3 by stopped flow CO2 hydrase assay
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Carbonic anhydrase 9
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: >1.00E+3nM
Assay Description:
Inhibition of recombinant human carbonic anhydrase 9 expressed in Escherichia coli GOLD BL21 (DE3) by stopped-flow CO2 hydration assay
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Carbonic anhydrase 12
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: >1.00E+3nM
Assay Description:
Inhibition of recombinant human carbonic anhydrase 12 expressed in Escherichia coli by stopped-flow CO2 hydration assay
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Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: >1.00E+3nM
Assay Description:
Inhibition of recombinant human carbonic anhydrase 1 expressed in Escherichia coli BL21 (DE3) by stopped-flow CO2 hydration assay
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Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: >1.00E+3nM
Assay Description:
Inhibition of recombinant human carbonic anhydrase 2 expressed in Escherichia coli BL21 (DE3) by stopped-flow CO2 hydration assay
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Carbonic anhydrase 6
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 1.21E+3nM ΔG°: -33.8kJ/mole
pH: 7.4 T: 2°C
Assay Description:
Carbonic anhydrase activity was assayed by following the change in absorbance at 348 nm of 4-nitrophenylacetate (NPA) to 4-nitrophenylate ion over a ...
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Carbonic anhydrase 5A, mitochondrial
(Mus musculus (mouse))
Universita Degli Studi Di Firenze
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 1.36E+3nM
Assay 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...
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Carbonic anhydrase 4
(Bos taurus (bovine))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 2.99E+3nM
Assay Description:
Inhibition of bovine CA4
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Carbonic anhydrase 4
(Bos taurus (bovine))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 3.00E+3nM
Assay Description:
Inhibition of bovine carbonic anhydrase IV from bovine lung microsomes
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Carbonic anhydrase 4
(Bos taurus (bovine))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 3.00E+3nM
Assay Description:
Inhibitory activity against bovine carbonic anhydrase isozyme IV isolated from bovine lung microsomes, by esterase assay method.
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Carbonic anhydrase 4
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 3.00E+3nM
Assay Description:
Inhibition of cloned isozyme, human carbonic anhydrase IV
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Carbonic anhydrase 4
(Bos taurus (bovine))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 3.00E+3nM
Assay Description:
Inhibitory activity against bovine lung microsomes carbonic anhydrase isozyme IV (bCA IV).
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Carbonic anhydrase 4
(Bos taurus (bovine))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
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Affinity Data
Ki: 3.00E+3nM
Assay Description:
Inhibitory activity against bovine carbonic anhydrase IV (CA4), isolated from bovine lung microsomes
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Carbonic anhydrase 4
(Bos taurus (bovine))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
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Affinity Data
Ki: 3.00E+3nM
Assay Description:
Inhibitory activity against bovine carbonic anhydrase IV
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Carbonic anhydrase 4
(Bos taurus (bovine))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 3.00E+3nM
Assay Description:
Inhibitory activity against bovine carbonic anhydrase IV (bCAIV)
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Carbonic anhydrase 4
(Bos taurus (bovine))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 3.00E+3nM
Assay Description:
Inhibition of bovine carbonic anhydrase IV (CAIV)
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Carbonic anhydrase 4
(Bos taurus (bovine))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 3.00E+3nM
Assay 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...
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Target
Carbonic anhydrase 4
(Bos taurus (bovine))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 3.00E+3nM
Assay Description:
Initial rates of 4-nitrophenyl acetate hydrolysis catalyzed by different CA isozymes were monitored spectrophotometrically at 400 nm. A molar absorpt...
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Target
Carbonic anhydrase 4
(Bos taurus (bovine))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 3.00E+3nM
Assay Description:
Inhibitory activity against bovine carbonic anhydrase IV (CA4), isolated from bovine lung microsomes
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Carbonic anhydrase 5B, mitochondrial
(Homo sapiens (Human))
Kochi Medical School
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 3.65E+3nM
Assay 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...
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Target
Carbonic anhydrase 5B, mitochondrial
(Homo sapiens (Human))
Kochi Medical School
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 3.65E+3nM
Assay Description:
Inhibition of human recombinant CA5B by stopped flow CO2 hydrase assay
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Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 3.85E+3nM
Assay Description:
Esterase activities of hCA I and hCA II isoenzymes, eluted from affinity column,were determined by hydrolysis of p-nitrophenylacetate. The change of ...
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Target
Carbonic anhydrase
(Methanosarcina thermophila)
Pennsylvania State University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 3.93E+3nM
Assay Description:
Inhibitory activity against alpha carbonic anhydrase (Co-Cam) from Methanosarcina thermophila
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Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 4.50E+3nM
Assay Description:
Esterase activities of hCA I and hCA II isoenzymes, eluted from affinity column,were determined by hydrolysis of p-nitrophenylacetate. The change of ...
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Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 5.00E+3nM
Assay Description:
Inhibition of human cloned carbonic anhydrase 1 preincubated for 15 mins by stopped flow CO2 hydration assay
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Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: >5.00E+3nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase1 after 15 mins by stopped flow carbondioxide hydrase assay method
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Target
Carbonic anhydrase 14
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 5.40E+3nM
Assay Description:
Inhibition of human CA14 preincubated for 15 mins by stopped-flow CO2 hydration method
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Target
Carbonic anhydrase 14
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 5.40E+3nM
Assay Description:
Inhibition of human full length cloned transmembrane carbonic anhydrase 14 preincubated for 15 mins by CO2 hydration stopped-flow assay
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Target
Carbonic anhydrase 14
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 5.40E+3nM
Assay Description:
Inhibitory constant against human carbonic anhydrase XIV in CO2 hydrase assay
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Target
Carbonic anhydrase 14
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 5.40E+3nM
Assay Description:
Inhibition of human recombinant CA14 by stopped flow CO2 hydrase assay
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Carbonic anhydrase
(Mycobacterium tuberculosis)
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 6.24E+3nM
Assay Description:
Inhibition of Mycobacterium tuberculosis recombinant beta-carbonic anhydrase Rv3273 preincubated for 15 mins by stopped-flow CO2 hydrase assay
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Target
Siderophore-binding protein
(Mycobacterium tuberculosis)
Universit?? Degli Studi Di Firenze
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 7.11E+3nM ΔG°: -29.4kJ/mole
pH: 7.5 T: 2°C
Assay Description:
An Applied Photophysics stopped-flow instrument has been used for assaying the CA-catalyzed CO2 hydration activity [Khalifah et al., J. Biol. Chem., ...
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Target
Carbonic anhydrase
(Mycobacterium tuberculosis)
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 7.11E+3nM
Assay Description:
Inhibition of Mycobacterium tuberculosis recombinant Rv3273 beta-carbonic anhydrase after 15 mins by stopped flow CO2 hydration assay
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Carbonic anhydrase
(Mycobacterium tuberculosis)
Kochi Medical School
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 7.11E+3nM ΔG°: -28.9kJ/mole
pH: 8.3 T: 2°C
Assay 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...
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Carbonic anhydrase
(Candida albicans (Yeast))
Universite Degli Studi Di Firenze
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 7.63E+3nM ΔG°: -28.7kJ/mole
pH: 8.3 T: 2°C
Assay 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...
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Carbonic anhydrase
(Candida albicans (Yeast))
Universite Degli Studi Di Firenze
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 7.63E+3nM
Assay Description:
Inhibition of Candida albicans recombinant Nce103 beta-carbonic anhydrase after 15 mins by stopped flow CO2 hydration assay
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Target
Carbonic anhydrase
(Astrosclera willeyana)
Slovak Academy Of Sciences
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 7.70E+3nM
Assay Description:
Inhibition of GST-tagged astrosclera willeyana Astrosclerin-3 expressed in Escherichia coli after 15 mins preincubation by stopped flow CO2 hydration...
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Beta-carbonic anhydrase 1
(Mycobacterium tuberculosis)
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 9.23E+3nM
Assay Description:
Inhibition of Mycobacterium tuberculosis recombinant beta-carbonic anhydrase Rv1284 preincubated for 15 mins by stopped-flow CO2 hydrase assay
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Target
Carbonic anhydrase 15 [19-324]
(Mus musculus (mouse))
University Of Tampere
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 9.61E+3nM ΔG°: -28.2kJ/mole
pH: 7.5 T: 2°C
Assay 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...
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Target
Carbonic anhydrase 15
(Mus musculus)
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 9.61E+3nM
Assay Description:
Inhibition of mouse recombinant CA15 by stopped flow CO2 hydrase assay
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Carbonic anhydrase 4
(Homo sapiens (Human))
Universit£
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ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 9.76E+3nM
Assay Description:
Inhibition of human recombinant CA4 by stopped flow CO2 hydrase assay
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Target
Carbonic anhydrase 4
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 9.76E+3nM
Assay Description:
Inhibitory activity against human carbonic anhydrase IV (hCAIV)
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Target
Carbonic anhydrase 4
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 9.76E+3nM
Assay Description:
Inhibition of human CA4 preincubated for 15 mins by stopped-flow CO2 hydration method
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Target
Beta-carbonic anhydrase 1
(Mycobacterium tuberculosis)
Universit£
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ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 9.84E+3nM ΔG°: -28.1kJ/mole
pH: 8.3 T: 2°C
Assay 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...
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Target
Beta-carbonic anhydrase 1
(Mycobacterium tuberculosis)
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 9.84E+3nM
Assay Description:
Inhibition of Mycobacterium tuberculosis recombinant Rv1284 beta-carbonic anhydrase after 15 mins by stopped flow CO2 hydration assay
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Target
Beta-carbonic anhydrase 1
(Mycobacterium tuberculosis)
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 9.84E+3nM ΔG°: -28.6kJ/mole
pH: 7.5 T: 2°C
Assay Description:
An Applied Photophysics stopped-flow instrument has been used for assaying the CA-catalyzed CO2 hydration activity [Khalifah et al., J. Biol. Chem., ...
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Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 1.01E+4nM
Assay Description:
Inhibition of human esterase activity of carbonic anhydrase 2 using 4-nitrophenylacetate as substrate after 3 mins by spectrophotometric analysis
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Target
Carbonic anhydrase
(Saccharomyces cerevisiae)
Balikesir University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 1.85E+4nM
Assay Description:
Inhibition of Saccharomyces cerevisiae recombinant CA expressed in Escherichia coli by stopped-flow CO2 hydrase assay
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Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 2.50E+4nM ΔG°: -26.3kJ/mole
pH: 7.5 T: 2°C
Assay 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...
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Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of human carbonic anhydrase-1 by stopped-flow CO2 hydration assay
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Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 1 by stopped-flow CO2 hydration assay
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Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of human recombinant Carbonic anhydrase 2 compound preincubated for 15 mins by stopped flow CO2 hydrase assay method
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
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ChEBI
CHEMBL
DrugBank
MCE
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 1 by stopped flow CO2 hydrase assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of human carbonic anhydrase 1 pre-incubated for 15 mins by stopped-flow CO2 hydration assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of recombinant human carbonic anhydrase-1 by stopped flow CO2 hydrase assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of human Carbonic anhydrase1 using CO2 as substrate preincubated for 15 mins by stopped-flow CO2 hydration assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of human carbonic anhydrase 1 incubated for 15 mins by stopped-flow CO2 hydration assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of recombinant human carbonic anhydrase 1 preincubated for 15 mins by stopped-flow CO2 hydration assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of wild type human recombinant carbonic anhydrase 1 expressed in Escherichia coli BL21 (DE3) after 15 mins by CO2 hydration method
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of human recombinant CA1 by stopped-flow CO2 hydration assay
Checked by Author
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of human recombinant alpha-carbonic anhydrase 1 after 15 mins by stopped flow CO2 hydration assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
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PDB
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+4nM
pH: 7.5
Assay Description:
Inhibition of human carbonic anhydrase I by spectrophotometry at pH 7.5
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of human full length cytosolic isoform of carbonic anhydrase 1 preincubated for 15 mins by stopped-flow CO2 hydration assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
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PDB
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+4nM
pH: 7.5
Assay Description:
Inhibition of human recombinant carbonic anhydrase 1 at pH 7.5 by stopped flow CO2 hydration assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of human carbonic anhydrase 1-catalyzed CO2 hydration activity by stopped flow assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 1 after 15 mins by stopped flow CO2 hydration assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of human recombinant CA1
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+4nM
Assay Description:
Ki value against human carbonic anhydrase I
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of human recombinant CA1 by CO2 hydration stopped flow assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of human recombinant cytosolic isozyme CA I by stopped-flow CO2 hydrase method
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 1 by stopped flow CO2 hydration assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 1 preincubated for 15 mins by CO2 hydration stopped-flow assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of human recombinant CA1 by stopped flow CO2 hydrase assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of human recombinant CA1 by stopped-flow CO2 assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of human recombinant CA1 by stopped-flow CO2 hydrase assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of recombinant human carbonic anhydrase 1 assessed as reduction in CO2 hydration preincubated for 15 mins followed by CO2 addition measure...
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase-1 preincubated for 10 mins by stopped-flow CO2 hydration assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of human carbonic anhydrase-1 assessed as reduction in CO2 hydration preincubated for 15 mins followed by CO2 addition measured for 10 to ...
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of human CA1 cytosolic isoform preincubated for 15 mins by stopped-flow CO2 hydration method
More data for this Ligand-Target Pair
Target Info
PDB
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UniProtKB/SwissProt
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Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
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Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of full length human cytosolic carbonic anhydrase 1 preincubated for 15 mins by stop flow CO2 hydrase assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
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ChEBI
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Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of full length human cytosolic carbonic anhydrase 1 preincubated for 15 mins by stop flow CO2 hydrase assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
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In Depth
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Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.55E+4nM
pH: 7.4
Assay Description:
CA activity was assayed by following the change in absorbance at 348 nm of 4-nitrophenylacetate (NPA) to 4-nitrophenylate ion over a period of 3 min ...
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
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In Depth
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Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.80E+4nM ΔG°: -25.7kJ/mole
pH: 7.5 T: 2°C
Assay 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
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
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MCE
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In Depth
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Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.80E+4nM
Assay Description:
Inhibition of human CA1
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
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MCE
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.80E+4nM
Assay Description:
Inhibition of human esterase activity of carbonic anhydrase 1 using 4-nitrophenylacetate as substrate after 3 mins by spectrophotometric analysis
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
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MCE
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PDB
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.80E+4nM
Assay Description:
Inhibition of human carbonic anhydrase I (CAI)
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
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MMDB
PC cid
PC sid
PDB
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.80E+4nM
Assay Description:
Inhibitory activity against human carbonic anhydrase I at 0.09 uM
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
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PDB
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.80E+4nM
Assay Description:
Inhibitory activity against human carbonic anhydrase I expressed in Escherichia coli BL21
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.80E+4nM
Assay Description:
Inhibitory potency against human cloned Carbonic anhydrase I expressed in Escherichia coli strain BL21
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.80E+4nM
Assay Description:
Inhibitory activity against human carbonic anhydrase I (hCAI)
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.80E+4nM
Assay Description:
Inhibitory activity against human carbonic anhydrase I
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.80E+4nM
Assay Description:
Inhibitory activity against Human carbonic anhydrase I
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.80E+4nM
Assay Description:
Inhibitory activity against human recombinant carbonic anhydrase I (CA1)
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.80E+4nM
Assay Description:
Inhibitory activity against human cloned carbonic anhydrase isozyme I (hCA I, cytosolic form).
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.80E+4nM
Assay Description:
Inhibitory activity against human carbonic anhydrase I (hCA I) by using esterase assay method
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.80E+4nM
Assay Description:
Inhibition of cloned isozyme, human carbonic anhydrase I
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
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MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.80E+4nM
Assay Description:
Inhibition of human carbonic anhydrase I
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.80E+4nM
Assay Description:
Inhibitory activity against human cloned carbonic anhydrase isozyme I by esterase assay method.
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.80E+4nM
Assay Description:
Inhibition of human carbonic anhydrase I (CAI)
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.80E+4nM
Assay Description:
Inhibitiory activity against human Carbonic anhydrase I (hCA I)
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.80E+4nM
Assay Description:
Inhibition constant against human recombinant carbonic anhydrase I
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.80E+4nM
Assay Description:
Inhibitory constant against human Carbonic anhydrase I
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.80E+4nM
Assay Description:
Inhibitory activity against human carbonic anhydrase I (CA1)
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
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MCE
KEGG
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PC cid
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.80E+4nM
Assay Description:
Inhibition of human carbonic anhydrase 2-catalyzed CO2 hydration preincubated for 10 mins by stopped-flow assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
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In Depth
Details
Article
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PDB
3D Structure (crystal)
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.80E+4nM
Assay Description:
Inhibition of human recombinant cytosolic human carbonic anhydrase-1 incubated for 15 mins prior to testing by stopped-flow CO2 hydrase assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.80E+4nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 1 preincubated for 15 mins by CO2 hydration stopped-flow assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
Patents
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.80E+4nM ΔG°: -26.0kJ/mole
pH: 7.4 T: 2°C
Assay Description:
Initial rates of 4-nitrophenyl acetate hydrolysis catalyzed by different CA isozymes were monitored spectrophotometrically at 400 nm. A molar absorpt...
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Carbonic anhydrase 2
(Mycobacterium tuberculosis)
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 2.96E+4nM
Assay Description:
Inhibition of full length Mycobacterium tuberculosis H37Rv recombinant carbonic anhydrase 2 encoded by RV3588c by stopped flow CO2 hydration assay
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Carbonic anhydrase 2
(Mycobacterium tuberculosis)
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 2.96E+4nM ΔG°: -25.8kJ/mole
pH: 7.5 T: 2°C
Assay Description:
An Applied Photophysics stopped-flow instrument has been used for assaying the CA-catalyzed CO2 hydration activity [Khalifah et al., J. Biol. Chem., ...
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Carbonic anhydrase 5A, mitochondrial
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 3.20E+4nM
Assay Description:
Inhibition of human recombinant CA5A by stopped flow CO2 hydrase assay
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Carbonic anhydrase 5A, mitochondrial
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 3.20E+4nM
Assay Description:
Inhibition of human mitochondrial CA5A preincubated for 15 mins by stopped-flow CO2 hydration method
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Carbonic anhydrase 5A, mitochondrial
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 3.20E+4nM
Assay 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...
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Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 4.29E+4nM
Assay Description:
Inhibition of cytosolic carbonic anhydrase 1 esterase activity isolated from human serum using 4-nitrophenylacetate as substrate measured over 3 mins...
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Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 4.29E+4nM ΔG°: -24.9kJ/mole
pH: 7.4 T: 2°C
Assay Description:
Carbonic anhydrase activity was assayed by following the change in absorbance at 348 nm of 4-nitrophenylacetate (NPA) to 4-nitrophenylate ion over a ...
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Carbonic anhydrase
(Methanobacterium thermoautotrophicum)
Pennsylvania State University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 5.78E+4nM
Assay Description:
Inhibitory activity against beta carbonic anhydrase (Cab) from Methanobacterium thermoautotrophicum
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Carbonic anhydrase 3
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: >1.00E+5nM
Assay Description:
Inhibition of human CA3 cytosolic isoform preincubated for 15 mins by stopped-flow CO2 hydration method
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Carbonic anhydrase 9
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 2.94E+5nM
Assay Description:
Inhibitory activity against human carbonic anhydrase IX at 0.09 uM
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Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 3.00E+5nM
Assay Description:
Inhibitory activity against human carbonic anhydrase II at 0.01 uM
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Target
Carbonic anhydrase 3
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 9.88E+5nM
Assay Description:
Inhibition of human recombinant CA 3 assessed as CO2 hydration by stopped flow kinetic assay
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Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Ki: 3.33E+6nM
Assay Description:
Inhibition of human carbonic anhydrase 2
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Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
IC50: 256nM
Assay Description:
Inhibition of recombinant human carbonic anhydrase 2 preincubated with enzyme for 15 mins by phenol red dye based stopped flow CO2 hydration assay
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Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
IC50: 260nM
Assay Description:
Inhibition of human recombinant CA2 using 4-nitrophenylacetate as substrate preincubated for 15 mins by stopped-flow CO2 hydration assay
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Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
IC50: 290nM
Assay Description:
Inhibition of human recombinant CA9 using 4-nitrophenylacetate as substrate preincubated for 15 mins by stopped-flow CO2 hydration assay
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Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
IC50: 298nM
Assay Description:
Inhibition of recombinant human carbonic anhydrase 9 preincubated with enzyme for 15 mins by phenol red dye based stopped flow CO2 hydration assay
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Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
IC50: 628nM
Assay Description:
Carbonic anhydrase activity was assayed by following the change in absorbance at 348 nm of 4-nitrophenylacetate (NPA) to 4-nitrophenylate ion over a ...
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Carbonic anhydrase 6
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
IC50: 1.21E+3nM
Assay Description:
Carbonic anhydrase activity was assayed by following the change in absorbance at 348 nm of 4-nitrophenylacetate (NPA) to 4-nitrophenylate ion over a ...
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Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
IC50: 2.40E+3nM
Assay Description:
Inhibitory concentration against human cystolic isozyme II of Carbonic anhydrase
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Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
IC50: 7.50E+3nM
Assay Description:
Inhibition of recombinant human carbonic anhydrase 2 using 4-nitrophenylacetate as substrate pretreated for 15 mins prior to test by spectrophotometr...
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Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
IC50: 1.20E+4nM
Assay Description:
Binding affinity towards HSV-1 thymidine kinase
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Carbonic anhydrase 5A, mitochondrial
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
IC50: 3.20E+4nM
Assay Description:
Inhibitory concentration against human cystolic isozyme V of Carbonic anhydrase
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Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
IC50: 4.29E+4nM
Assay Description:
Carbonic anhydrase activity was assayed by following the change in absorbance at 348 nm of 4-nitrophenylacetate (NPA) to 4-nitrophenylate ion over a ...
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Target
Cholinesterase
(Homo sapiens (Human))
University Of Education
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
IC50: 1.38E+5nM
Assay Description:
Inhibition of BuChE (unknown origin) using butyrylthiocholine bromide as substrate by Ellman method
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Acetylcholinesterase
(Homo sapiens (Human))
University Of Education
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
IC50: 1.45E+5nM
Assay Description:
Inhibition of AChE (unknown origin) using acetylcholine iodide as substrate by Ellman method
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Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Kd: 5.55E+3nM
Assay Description:
Binding affinity to GST-fused human carbonic anhydrase-2 expressed in Escherichia coli BL21 codon plus cells assessed as dissociation constant by SPR...
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Target
Carbonic anhydrase 2
(Bos taurus)
The University Of Tokushima Graduate School
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Kd: 5.88E+3nM
Assay Description:
Binding affinity to bovine carbonic anhydrase-2 assessed as dissociation constant by SPR method
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Target
Protein argonaute-2
(Homo sapiens)
Gifu University
Curated by
ChEMBL
Ligand
BDBM10857
(4-aminobenzene-1-sulfonamide | CHEMBL21 | Sulfanil...)
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Affinity Data
Kd: 1.70E+4nM
Assay Description:
Binding affinity to human Argonaut protein 2 PAZ domain assessed as dissociation constant by using isothermal titration microcalorimetry
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
GoogleScholar
Ligand Info
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ChEBI
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
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