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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
(change energy unit to
kcal/mol
)
Found
32
hits in this display
Target
Metallo-beta-lactamase VIM-2
(Pseudomonas aeruginosa (g-Proteobacteria))
Individual
US Patent
Ligand
BDBM580195
(US11491146, Compound 2b)
Copy SMILES
Copy InChI
Affinity Data
Ki: 217nM
Assay Description:
To identify potential MBL inhibitors, the relative change in the formation of hydrolyzed nitrocefin between treated and untreated VIM2 was determined...
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US Patent
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Target
Carbonic anhydrase 3
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM50366038
(CHEMBL1356238)
Copy SMILES
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Affinity Data
Ki: 1.62E+3nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 3 preincubated for 15 mins to 72 hrs measured after 6 hrs by stopped flow CO2 hydration method
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Target
Carbonic anhydrase 3
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM50366038
(CHEMBL1356238)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1.62E+3nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 3 preincubated for 15 mins to 72 hrs measured after 15 mins by stopped flow CO2 hydration method
More data for this Ligand-Target Pair
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Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM50366038
(CHEMBL1356238)
Copy SMILES
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Affinity Data
Ki: 1.72E+3nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 9 preincubated for 15 mins to 72 hrs measured after 6 hrs by stopped flow CO2 hydration method
More data for this Ligand-Target Pair
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Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM50366038
(CHEMBL1356238)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1.72E+3nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 9 preincubated for 15 mins to 72 hrs measured after 15 mins by stopped flow CO2 hydration method
More data for this Ligand-Target Pair
Target Info
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Target
Carbonic anhydrase 6
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM50366038
(CHEMBL1356238)
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Affinity Data
Ki: 2.41E+3nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 6 preincubated for 15 mins to 72 hrs measured after 6 hrs by stopped flow CO2 hydration method
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Target
Carbonic anhydrase 6
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM50366038
(CHEMBL1356238)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.41E+3nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 6 preincubated for 15 mins to 72 hrs measured after 15 mins by stopped flow CO2 hydration method
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Target
Carbonic anhydrase 14
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM50366038
(CHEMBL1356238)
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Affinity Data
Ki: 2.91E+3nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 14 preincubated for 15 mins to 72 hrs measured after 6 hrs by stopped flow CO2 hydration method
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Target
Carbonic anhydrase 14
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM50366038
(CHEMBL1356238)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.91E+3nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 14 preincubated for 15 mins to 72 hrs measured after 15 mins by stopped flow CO2 hydration method
More data for this Ligand-Target Pair
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Target
Carbonic anhydrase 5B, mitochondrial
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM50366038
(CHEMBL1356238)
Copy SMILES
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Affinity Data
Ki: 3.55E+3nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 5B preincubated for 15 mins to 72 hrs measured after 6 hrs by stopped flow CO2 hydration method
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Target
Carbonic anhydrase 5B, mitochondrial
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM50366038
(CHEMBL1356238)
Copy SMILES
Copy InChI
Affinity Data
Ki: 3.55E+3nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 5B preincubated for 15 mins to 72 hrs measured after 15 mins by stopped flow CO2 hydration method
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Carbonic anhydrase 13
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM50366038
(CHEMBL1356238)
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Affinity Data
Ki: 4.15E+3nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 13 preincubated for 15 mins to 72 hrs measured after 6 hrs by stopped flow CO2 hydration method
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
BDBM50366038
(CHEMBL1356238)
Copy SMILES
Copy InChI
Affinity Data
Ki: 4.15E+3nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 13 preincubated for 15 mins to 72 hrs measured after 15 mins by stopped flow CO2 hydration method
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Target
Carbonic anhydrase 5A, mitochondrial
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM50366038
(CHEMBL1356238)
Copy SMILES
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Affinity Data
Ki: 5.12E+3nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 5A preincubated for 15 mins to 72 hrs measured after 15 mins by stopped flow CO2 hydration method
More data for this Ligand-Target Pair
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Target
Carbonic anhydrase 5A, mitochondrial
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM50366038
(CHEMBL1356238)
Copy SMILES
Copy InChI
Affinity Data
Ki: 5.12E+3nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 5A preincubated for 15 mins to 72 hrs measured after 6 hrs by stopped flow CO2 hydration method
More data for this Ligand-Target Pair
Target Info
Reactome pathway
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Target
Carbonic anhydrase 12
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM50366038
(CHEMBL1356238)
Copy SMILES
Copy InChI
Affinity Data
Ki: 5.40E+3nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 12 preincubated for 15 mins to 72 hrs measured after 6 hrs by stopped flow CO2 hydration method
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
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KEGG
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Target
Carbonic anhydrase 12
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM50366038
(CHEMBL1356238)
Copy SMILES
Copy InChI
Affinity Data
Ki: 5.40E+3nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 12 preincubated for 15 mins to 72 hrs measured after 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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ChEBI
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Article
PubMed
Copy BDB DOI
Target
Carbonic anhydrase 4
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM50366038
(CHEMBL1356238)
Copy SMILES
Copy InChI
Affinity Data
Ki: 6.13E+3nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 4 preincubated for 15 mins to 72 hrs measured after 6 hrs by stopped flow CO2 hydration method
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
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KEGG
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Target
Carbonic anhydrase 4
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM50366038
(CHEMBL1356238)
Copy SMILES
Copy InChI
Affinity Data
Ki: 6.13E+3nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 4 preincubated for 15 mins to 72 hrs measured after 15 mins by stopped flow CO2 hydration method
More data for this Ligand-Target Pair
Target Info
PDB
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Target
Carbonic anhydrase 7
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM50366038
(CHEMBL1356238)
Copy SMILES
Copy InChI
Affinity Data
Ki: 7.76E+3nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 7 preincubated for 15 mins to 72 hrs measured after 6 hrs by stopped flow CO2 hydration method
More data for this Ligand-Target Pair
Target Info
PDB
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KEGG
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Target
Carbonic anhydrase 7
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM50366038
(CHEMBL1356238)
Copy SMILES
Copy InChI
Affinity Data
Ki: 7.76E+3nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 7 preincubated for 15 mins to 72 hrs measured after 15 mins by stopped flow CO2 hydration method
More data for this Ligand-Target Pair
Target Info
PDB
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Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM50366038
(CHEMBL1356238)
Copy SMILES
Copy InChI
Affinity Data
Ki: >2.00E+5nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 1 preincubated for 15 mins to 72 hrs measured after 6 hrs by stopped flow CO2 hydration method
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
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Target
Carbonic anhydrase 2
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM50366038
(CHEMBL1356238)
Copy SMILES
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Affinity Data
Ki: >2.00E+5nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 2 preincubated for 15 mins to 72 hrs measured after 6 hrs by stopped flow CO2 hydration method
More data for this Ligand-Target Pair
Target Info
PDB
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MMDB
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Target
Carbonic anhydrase 2
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM50366038
(CHEMBL1356238)
Copy SMILES
Copy InChI
Affinity Data
Ki: >2.00E+5nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 2 preincubated for 15 mins to 72 hrs measured after 15 mins by stopped flow CO2 hydration method
More data for this Ligand-Target Pair
Target Info
PDB
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Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM50366038
(CHEMBL1356238)
Copy SMILES
Copy InChI
Affinity Data
Ki: >2.00E+5nM
Assay Description:
Inhibition of human recombinant carbonic anhydrase 1 preincubated for 15 mins to 72 hrs measured after 15 mins by stopped flow CO2 hydration method
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
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Target
Metallo-beta-lactamase VIM-2
(Pseudomonas aeruginosa (g-Proteobacteria))
Individual
US Patent
Ligand
BDBM580195
(US11491146, Compound 2b)
Copy SMILES
Copy InChI
Affinity Data
IC50: 908nM
Assay Description:
To identify potential MBL inhibitors, the relative change in the formation of hydrolyzed nitrocefin between treated and untreated VIM2 was determined...
More data for this Ligand-Target Pair
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Target
Lysyl oxidase homolog 3
(Homo sapiens (Human))
Hungarian Academy Of Sciences
Curated by
ChEMBL
Ligand
BDBM50366038
(CHEMBL1356238)
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Affinity Data
IC50: 1.20E+4nM
Assay Description:
Inhibition of recombinant human LOXL3 expressed in CHO cells using diaminopentane as substrate preincubated for 30 mins followed by substrate additio...
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Target
Lysyl oxidase homolog 4
(Homo sapiens)
Hungarian Academy Of Sciences
Curated by
ChEMBL
Ligand
BDBM50366038
(CHEMBL1356238)
Copy SMILES
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Affinity Data
IC50: 1.50E+4nM
Assay Description:
Inhibition of recombinant human LOXL4 expressed in baculovirus infected insect cells using diaminopentane as substrate preincubated for 30 mins follo...
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Target
Lysyl oxidase homolog 2
(Homo sapiens (Human))
Hungarian Academy Of Sciences
Curated by
ChEMBL
Ligand
BDBM50366038
(CHEMBL1356238)
Copy SMILES
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Affinity Data
IC50: 1.80E+4nM
Assay Description:
Inhibition of recombinant LOXL2 (unknown origin) expressed in NS0 cells using diaminopentane as substrate preincubated for 30 mins followed by substr...
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Target
Stromelysin-1
(Homo sapiens (Human))
TBA
Ligand
BDBM50366038
(CHEMBL1356238)
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Affinity Data
IC50: 2.00E+4nM
Assay Description:
Inhibition of MMP-3 (unknown origin) by Colorimetric assay
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Protein-lysine 6-oxidase
(Homo sapiens (Human))
Hungarian Academy Of Sciences
Curated by
ChEMBL
Ligand
BDBM50366038
(CHEMBL1356238)
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Affinity Data
IC50: 3.30E+4nM
Assay Description:
Inhibition of recombinant human LOX expressed in HEK293 cells using diaminopentane as substrate preincubated for 30 mins followed by substrate additi...
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Target
Stromelysin-1
(Homo sapiens (Human))
TBA
Ligand
BDBM50366038
(CHEMBL1356238)
Copy SMILES
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Affinity Data
IC50: 3.50E+4nM
Assay Description:
Inhibition of MMP-3 (unknown origin) by fluorescence based assay
More data for this Ligand-Target Pair
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