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Compile Data Set for Download or QSAR
maximum 50k data
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
(change energy unit to
kcal/mol
)
Found
168
hits in this display
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
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Affinity Data
Ki: 0.00600nM
Assay Description:
Inhibition of human CA2
More data for this Ligand-Target Pair
Target Info
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Target
Carbonic anhydrase 12
(Homo sapiens (Human))
Griffith University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
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Affinity Data
Ki: 0.300nM
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
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Target
Carbonic anhydrase 12
(Homo sapiens (Human))
Griffith University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 0.300nM
Assay Description:
Inhibition of human recombinant CA12 by stopped flow CO2 hydration assay
More data for this Ligand-Target Pair
Target Info
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Target
Carbonic anhydrase 12
(Homo sapiens (Human))
Griffith University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 0.300nM
Assay Description:
Ki value against human carbonic anhydrase XII (hCA XII)
More data for this Ligand-Target Pair
Target Info
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Target
Carbonic anhydrase 12
(Homo sapiens (Human))
Griffith University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 0.300nM
Assay Description:
Inhibitory constant against catalytic domain of human carbonic anhydrase XII
More data for this Ligand-Target Pair
Target Info
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Target
Carbonic anhydrase 13
(Mus musculus (mouse))
Universit£
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
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Affinity Data
Ki: 41nM
Assay Description:
Ki value against murine carbonic anhydrase XIII
More data for this Ligand-Target Pair
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Target
Carbonic anhydrase 13
(Mus musculus (mouse))
Universit£
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 41nM
Assay Description:
Inhibitory activity against murine carbonic anhydrase XIII (mCA XIII) by using CO2 hydrase assay method
More data for this Ligand-Target Pair
Target Info
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Target
Carbonic anhydrase 7
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
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Affinity Data
Ki: 75nM
Assay Description:
Ki value against human carbonic anhydrase VII
More data for this Ligand-Target Pair
Target Info
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Target
Carbonic anhydrase
(Stylophora pistillata)
Centre Scientifique De Monaco
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 82.5nM
Assay Description:
Inhibition of Stylophora pistillata carbonic anhydrase by stopped-flow CO2 hydration assay
Checked by Author
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Target
Carbonic anhydrase
(Stylophora pistillata)
Centre Scientifique De Monaco
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 82.5nM
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
Target Info
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Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 103nM
Assay Description:
Inhibitory activity against human carbonic anhydrase IX expressed in Escherichia coli BL21
More data for this Ligand-Target Pair
Target Info
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KEGG
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Copy BDB DOI
Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 103nM
Assay Description:
Inhibition of catalytic domain of human recombinant CA IX
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
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antibodypedia
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Ligand Info
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CHEMBL
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In Depth
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Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 103nM
Assay Description:
Inhibition of human recombinant CA9 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
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CHEMBL
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 103nM
Assay Description:
Inhibitory constant against human Carbonic anhydrase IX
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
CHEMBL
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MCE
KEGG
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PC sid
PDB
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 103nM
Assay Description:
Inhibitory constant against catalytic domain of human carbonic anhydrase IX
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
CHEMBL
DrugBank
MCE
KEGG
PC cid
PC sid
PDB
Patents
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 103nM
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
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
CHEMBL
DrugBank
MCE
KEGG
PC cid
PC sid
PDB
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 103nM
Assay Description:
Inhibitory activity against human tumor-associated transmembrane carbonic anhydrase IX.
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
CHEMBL
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MCE
KEGG
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PC sid
PDB
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 103nM
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
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
CHEMBL
DrugBank
MCE
KEGG
PC cid
PC sid
PDB
Patents
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 103nM
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
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
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CHEMBL
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In Depth
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PubMed
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
Assay Description:
Inhibitory activity against human carbonic anhydrase II expressed in Escherichia coli BL21
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
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Ligand Info
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CHEMBL
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In Depth
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PubMed
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
Assay Description:
Inhibition of human recombinant CA2
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
CHEMBL
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KEGG
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In Depth
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PubMed
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
Assay Description:
Ki value against human carbonic anhydrase II (hCA II)
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
CHEMBL
DrugBank
MCE
KEGG
PC cid
PC sid
PDB
Patents
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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
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
Assay Description:
Ki value against human carbonic anhydrase II
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
CHEMBL
DrugBank
MCE
KEGG
PC cid
PC sid
PDB
Patents
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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
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
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
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
CHEMBL
DrugBank
MCE
KEGG
PC cid
PC sid
PDB
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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
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
Assay Description:
Inhibition of human carbonic anhydrase II (CAII)
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
CHEMBL
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KEGG
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PC sid
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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
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
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
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
CHEMBL
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MCE
KEGG
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PC sid
PDB
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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
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
Assay Description:
Inhibition of human recombinant CA2 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
CHEMBL
DrugBank
MCE
KEGG
PC cid
PC sid
PDB
Patents
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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
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
Assay Description:
Inhibition of human recombinant CA2 by stopped-flow CO2 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
CHEMBL
DrugBank
MCE
KEGG
PC cid
PC sid
PDB
Patents
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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
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
Assay Description:
Inhibition of human recombinant CA2 by stopped-flow 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
CHEMBL
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MCE
KEGG
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PC sid
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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
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
Assay Description:
Inhibition of human recombinant CA2 by stopped-flow CO2 hydrase 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
CHEMBL
DrugBank
MCE
KEGG
PC cid
PC sid
PDB
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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
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
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
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
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Ligand Info
Purchase
CHEMBL
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MCE
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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
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
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
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Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
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
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Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
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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Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
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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Reactome pathway
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Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
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
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM ΔG°: -38.6kJ/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. Phenol red has been used as indic...
More data for this Ligand-Target Pair
Target Info
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Reactome pathway
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Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
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
Target Info
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Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
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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Reactome pathway
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Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
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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MMDB
NCI pathway
Reactome pathway
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Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
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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MMDB
Reactome pathway
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Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
Assay Description:
Inhibitory activity against human carbonic anhydrase II (CA2)
More data for this Ligand-Target Pair
Target Info
PDB
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Reactome pathway
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Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
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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MMDB
Reactome pathway
KEGG
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Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
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
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Reactome pathway
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Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
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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Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
Assay Description:
Inhibitory constant against human Carbonic anhydrase II
More data for this Ligand-Target Pair
Target Info
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MMDB
Reactome pathway
KEGG
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Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
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
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Ligand Info
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Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
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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Ligand Info
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CHEMBL
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PubMed
Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
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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Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
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
PDB
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Reactome pathway
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Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
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
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
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Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
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
UniProtKB/SwissProt
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Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
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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Ligand Info
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Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
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
PDB
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Reactome pathway
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Ligand Info
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Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
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
PDB
MMDB
Reactome pathway
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Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
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
PDB
MMDB
Reactome pathway
KEGG
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Ligand Info
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Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
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
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Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
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
PDB
MMDB
Reactome pathway
KEGG
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Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
Assay Description:
Inhibition of 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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Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
Assay Description:
Inhibition of human carbonic anhydrase II
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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Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
Assay Description:
Inhibition of cloned isozyme, human carbonic anhydrase II
More data for this Ligand-Target Pair
Target Info
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Reactome pathway
KEGG
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Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 170nM
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
PDB
MMDB
Reactome pathway
KEGG
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Copy BDB DOI
Target
Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 170nM
Assay Description:
Inhibitory activity against human recombinant carbonic anhydrase II
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Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 170nM
Assay Description:
Inhibitory activity against human recombinant carbonic anhydrase II (CA2)
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Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 170nM
Assay Description:
Inhibitory activity against Human carbonic anhydrase II
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Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 170nM
Assay Description:
Inhibitory activity against human carbonic anhydrase II (hCAII)
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Carbonic anhydrase, alpha family
(Thiomicrospira crunogena (strain XCL-2))
Universit£
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 202nM
Assay Description:
Inhibition of recombinant Thiomicrospira crunogena XCL-2 carbonic anhydrase by stopped flow CO2 hydrase assay
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Carbonic anhydrase
(Methanosarcina thermophila)
Pennsylvania State University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 350nM
Assay Description:
Inhibitory activity against alpha carbonic anhydrase (Zn-Cam) from Methanosarcina thermophila
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Carbonic anhydrase
(Sulfurihydrogenibium sp. (strain YO3AOP1))
Universit£
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 350nM
Assay Description:
Inhibition of recombinant Sulfurihydrogenibium yellowstonense YO3AOP1 carbonic anhydrase by stopped flow CO2 hydrase assay
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Delta carbonic anhydrase
(Thalassiosira weissflogii)
Universit£
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 424nM
Assay Description:
Inhibition of Thalassiosira weissflogii delta carbonic anhydrase preincubated for 15 mins by stopped flow CO2 hydration assay
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Carbonic anhydrase
(Saccharomyces cerevisiae)
Balikesir University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 433nM
Assay Description:
Inhibition of Saccharomyces cerevisiae recombinant CA expressed in Escherichia coli by stopped-flow CO2 hydrase assay
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Carbonic anhydrase
(Stylophora pistillata)
Centre Scientifique De Monaco
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 508nM
Assay Description:
Inhibition of Stylophora pistillata carbonic anhydrase 2 by stopped-flow CO2 hydration assay
Checked by Author
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Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 612nM ΔG°: -35.5kJ/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 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 612nM
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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Carbonic anhydrase
(Helicobacter pylori (strain G27))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 830nM
Assay Description:
Inhibition of Helicobacter pylori recombinant CA
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CARBONIC ANHYDRASE
(Helicobacter pylori J99)
Kochi Medical School
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 873nM
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 5A, mitochondrial
(Mus musculus (mouse))
Universita Degli Studi Di Firenze
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 920nM
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 15 [19-324]
(Mus musculus (mouse))
University of Tampere
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 970nM ΔG°: -33.7kJ/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...
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Carbonic anhydrase
(Astrosclera willeyana)
Slovak Academy Of Sciences
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 973nM
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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Carbonic anhydrase 6
(Homo sapiens (Human))
Ondokuz Mayis University
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 1.01E+3nM ΔG°: -34.2kJ/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
(Candida albicans (Yeast))
Universite Degli Studi Di Firenze
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 1.11E+3nM ΔG°: -33.4kJ/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 4
(Bos taurus (bovine))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 2.79E+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
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 2.80E+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
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 2.80E+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
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 2.80E+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
(Bos taurus (bovine))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 2.80E+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
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 2.80E+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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Carbonic anhydrase 4
(Bos taurus (bovine))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 2.80E+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
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 2.80E+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
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 2.80E+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
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 2.80E+3nM
Assay Description:
Inhibition of bovine carbonic anhydrase IV from bovine lung microsomes
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Carbonic anhydrase 4
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 2.80E+3nM
Assay Description:
Inhibition of cloned isozyme, human carbonic anhydrase IV
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Carbonic anhydrase 14
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 3.20E+3nM
Assay Description:
Inhibitory constant against human carbonic anhydrase XIV in CO2 hydrase assay
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Carbonic anhydrase 14
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 3.20E+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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Carbonic anhydrase 6
(Homo sapiens (Human))
Ondokuz Mayis University
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 4.80E+3nM
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))
Ondokuz Mayis University
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 4.80E+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 6
(Homo sapiens (Human))
Ondokuz Mayis University
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 4.80E+3nM
Assay Description:
Inhibition of full length human recombinant CA VI
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Carbonic anhydrase
(Mycobacterium tuberculosis)
Kochi Medical School
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 7.33E+3nM ΔG°: -28.8kJ/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
(Mycobacterium tuberculosis)
Universit£
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 7.33E+3nM
Assay Description:
Inhibition of Mycobacterium tuberculosis recombinant carbonic anhydrase Rv3273 by stopped flow CO2 hydration assay
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Carbonic anhydrase
(Methanosarcina thermophila)
Pennsylvania State University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 8.50E+3nM
Assay Description:
Inhibitory activity against alpha carbonic anhydrase (Co-Cam) from Methanosarcina thermophila
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Carbonic anhydrase 4
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 8.60E+3nM
Assay Description:
Inhibitory activity against human carbonic anhydrase IV (hCAIV)
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Beta-carbonic anhydrase 1
(Mycobacterium tuberculosis)
Universit£
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 8.69E+3nM
Assay Description:
Inhibition of Mycobacterium tuberculosis recombinant carbonic anhydrase Rv1284 by stopped flow CO2 hydration assay
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Beta-carbonic anhydrase 1
(Mycobacterium tuberculosis)
Universit£
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 8.69E+3nM ΔG°: -28.4kJ/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 5B, mitochondrial
(Homo sapiens (Human))
Kochi Medical School
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 1.23E+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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Carbonic anhydrase
(Anopheles gambiae)
University Of Tampere And Tampere University Hospital
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 1.36E+4nM
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 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 1.71E+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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Carbonic anhydrase
(Cryptococcus neoformans var. grubii (Filobasidiell...)
Universite Degli Studi Di Firenze
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 1.85E+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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Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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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
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 2.50E+4nM ΔG°: -26.3kJ/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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Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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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
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Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of human carbonic anhydrase 2-catalyzed CO2 hydration preincubated for 10 mins by stopped-flow assay
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Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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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
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibitory activity against human carbonic anhydrase I (CA1)
More data for this Ligand-Target Pair
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Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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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
More data for this Ligand-Target Pair
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Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 1 by stopped flow CO2 hydrase assay
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Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibitory constant against human Carbonic anhydrase I
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Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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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
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Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of human recombinant Carbonic anhydrase 1 compound preincubated for 15 mins by stopped flow CO2 hydrase assay method
More data for this Ligand-Target Pair
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Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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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
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Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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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
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Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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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
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Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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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
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Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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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
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Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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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
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Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
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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
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Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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
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Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of human cloned 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
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Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+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
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PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+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
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Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+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
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Ligand Info
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CHEMBL
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Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+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
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Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+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
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PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+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
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Ligand Info
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Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+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
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Ligand Info
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PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+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
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Ligand Info
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PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+4nM
Assay Description:
Ki value 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
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Ligand Info
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Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+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
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KEGG
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Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+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
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KEGG
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Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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
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Ligand Info
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In Depth
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PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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
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Ligand Info
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CHEMBL
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In Depth
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PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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
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Ligand Info
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CHEMBL
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PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+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
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Ligand Info
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CHEMBL
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PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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
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PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+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
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KEGG
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Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+4nM
Assay Description:
Inhibition of human recombinant CA1 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
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Ligand Info
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PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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
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Ligand Info
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CHEMBL
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PubMed
Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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
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Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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
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Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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
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KEGG
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Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.50E+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
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Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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
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Copy BDB DOI
Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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
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Target
Carbonic anhydrase 5A, mitochondrial
(Homo sapiens (Human))
Kochi Medical School
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.76E+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...
More data for this Ligand-Target Pair
Target Info
Reactome pathway
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Target
Carbonic anhydrase
(Methanobacterium thermoautotrophicum)
Pennsylvania State University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.85E+4nM
Assay Description:
Inhibitory activity against beta carbonic anhydrase (Cab) from Methanobacterium thermoautotrophicum
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
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Target
Carbonic anhydrase 2
(Mycobacterium tuberculosis)
Universit£
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 3.07E+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 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 4.19E+4nM ΔG°: -25.0kJ/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 1
(Homo sapiens (Human))
Enscm/Umii/Umr-Cnrs 5635
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 4.19E+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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Carbonic anhydrase 9
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 1.03E+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
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 1.70E+5nM
Assay Description:
Inhibitory activity against human carbonic anhydrase II at 0.01 uM
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Serum paraoxonase/arylesterase 1
(Homo sapiens (Human))
AtatÜRk University
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 3.40E+5nM IC50: 1.90E+5nM
Assay Description:
The inhibitory effects of six sulfonamide derivatives was examined against the purified enzyme hPON1 and were tested in a triplicate experiment in fi...
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Carbonic anhydrase 3
(Homo sapiens (Human))
Kochi Medical School
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 6.81E+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
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
Ki: 5.88E+6nM
Assay Description:
Inhibition of human carbonic anhydrase 2
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Carbonic anhydrase 2
(Homo sapiens (Human))
A.P.S. University
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
IC50: 4.00E+3nM
Assay Description:
Inhibitory concentration against human cystolic isozyme II of Carbonic anhydrase
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Carbonic anhydrase 5A, mitochondrial
(Homo sapiens (Human))
Kochi Medical School
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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IC50: 2.76E+4nM
Assay Description:
Inhibitory concentration against human cystolic isozyme V of Carbonic anhydrase
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Bile salt export pump
(Homo sapiens (Human))
Amgen
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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IC50: >1.33E+5nM
Assay Description:
Inhibition of human BSEP overexpressed in Sf9 cell membrane vesicles assessed as uptake of [3H]-taurocholate in presence of ATP measured after 15 to ...
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ATP-binding cassette sub-family C member 4
(Homo sapiens (Human))
Amgen
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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IC50: >1.33E+5nM
Assay Description:
Inhibition of human MRP4 overexpressed in Sf9 cell membrane vesicles assessed as uptake of [3H]-estradiol-17beta-D-glucuronide in presence of ATP and...
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ATP-binding cassette sub-family C member 3
(Homo sapiens (Human))
Amgen
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
IC50: >1.33E+5nM
Assay Description:
Inhibition of human MRP3 overexpressed in Sf9 insect cell membrane vesicles assessed as uptake of [3H]-estradiol-17beta-D-glucuronide in presence of ...
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ATP-binding cassette sub-family C member 2
(Homo sapiens (Human))
Amgen
Curated by
ChEMBL
Ligand
BDBM10860
(4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 |...)
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Affinity Data
IC50: >1.33E+5nM
Assay Description:
Inhibition of human MRP2 overexpressed in Sf9 cell membrane vesicles assessed as uptake of [3H]-estradiol-17beta-D-glucuronide in presence of ATP and...
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