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Compile Data Set for Download or QSAR
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
(change energy unit to
kcal/mol
)
Found
6
hits in this display
Target
Plasmepsin I
(Plasmodium falciparum)
LinköPing University
Curated by
ChEMBL
Ligand
BDBM7985
((3S,4S)-5-[(4-bromophenyl)methoxy]-N-butyl-3-hydro...)
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Affinity Data
Ki: 8.10nM
Assay Description:
Inhibitory concentration against the Plasmepsin I of Plasmodium falciparum
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Plasmepsin I
(Plasmodium falciparum)
LinköPing University
Curated by
ChEMBL
Ligand
BDBM7985
((3S,4S)-5-[(4-bromophenyl)methoxy]-N-butyl-3-hydro...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 8.10nM
Assay Description:
Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Plasmepsin II
(Plasmodium falciparum)
Linkoping University
Ligand
BDBM7985
((3S,4S)-5-[(4-bromophenyl)methoxy]-N-butyl-3-hydro...)
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Copy InChI
Affinity Data
Ki: 68nM ΔG°: -40.5kJ/mole
pH: 4.5 T: 2°C
Assay Description:
Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Plasmepsin II
(Plasmodium falciparum)
Linkoping University
Ligand
BDBM7985
((3S,4S)-5-[(4-bromophenyl)methoxy]-N-butyl-3-hydro...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 68nM
Assay Description:
Inhibitory concentration against the Plasmepsin II of Plasmodium falciparum
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Cathepsin D
(Homo sapiens (Human))
LinköPing University
Curated by
ChEMBL
Ligand
BDBM7985
((3S,4S)-5-[(4-bromophenyl)methoxy]-N-butyl-3-hydro...)
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Copy InChI
Affinity Data
Ki: 473nM
Assay Description:
Inhibitory concentration against the human Cathepsin D
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
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Cathepsin D
(Homo sapiens (Human))
LinköPing University
Curated by
ChEMBL
Ligand
BDBM7985
((3S,4S)-5-[(4-bromophenyl)methoxy]-N-butyl-3-hydro...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 473nM
Assay Description:
Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...
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
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI