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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
6
hits in this display
Target
Procathepsin L
(Homo sapiens (Human))
Ewha Womans University
Curated by
ChEMBL
Ligand
BDBM50249605
(3-acetyl-5,8-dibromo-2-(4-bromophenylamino)quinoli...)
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Affinity Data
IC50: 1.06E+3nM
Assay Description:
Inhibition of human liver cathepsin L after 30 mins by fluorometric end-point assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
In Depth
Details
Article
PubMed
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Target
Cathepsin B
(Homo sapiens (Human))
Ewha Womans University
Curated by
ChEMBL
Ligand
BDBM50249605
(3-acetyl-5,8-dibromo-2-(4-bromophenylamino)quinoli...)
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Affinity Data
IC50: 1.64E+3nM
Assay Description:
Inhibition of human liver cathepsin B after 30 mins by fluorometric end-point assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Calpain-1 catalytic subunit
(Homo sapiens (Human))
Ewha Womans University
Curated by
ChEMBL
Ligand
BDBM50249605
(3-acetyl-5,8-dibromo-2-(4-bromophenylamino)quinoli...)
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Copy InChI
Affinity Data
IC50: 1.69E+3nM
Assay Description:
Inhibition of human erythrocytes mu-calpain by fluorometric assay using pep2 as substrate
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Calpain-1 catalytic subunit
(Homo sapiens (Human))
Ewha Womans University
Curated by
ChEMBL
Ligand
BDBM50249605
(3-acetyl-5,8-dibromo-2-(4-bromophenylamino)quinoli...)
Copy SMILES
Copy InChI
Affinity Data
IC50: 3.59E+3nM
Assay Description:
Inhibition of human erythrocytes mu-calpain after 30 mins by fluorometric assay using pep1 as substrate
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Pro-cathepsin H
(Homo sapiens (Human))
Ewha Womans University
Curated by
ChEMBL
Ligand
BDBM50249605
(3-acetyl-5,8-dibromo-2-(4-bromophenylamino)quinoli...)
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Copy InChI
Affinity Data
IC50: 9.18E+4nM
Assay Description:
Inhibition of human liver cathepsin H after 30 mins by fluorometric end-point assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Cathepsin D
(Homo sapiens (Human))
Ewha Womans University
Curated by
ChEMBL
Ligand
BDBM50249605
(3-acetyl-5,8-dibromo-2-(4-bromophenylamino)quinoli...)
Copy SMILES
Copy InChI
Affinity Data
IC50: >1.00E+5nM
Assay Description:
Inhibition of human liver cathepsin D after 30 mins by fluorometric end-point 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
CHEMBL
PC cid
PC sid
In Depth
Details
Article
PubMed
Copy BDB DOI