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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
16
hits in this display
Target
Neprilysin
(Oryctolagus cuniculus (rabbit))
University Of Paris
Curated by
ChEMBL
Ligand
BDBM50115843
((2S)-2-[(2R)-2-[(1R)-5-bromo-2,3-dihydro-1H-inden-...)
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Affinity Data
Ki: 1.80nM
Assay Description:
In vitro inhibition of Neutral endopeptidase.
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
Neprilysin
(Oryctolagus cuniculus (rabbit))
University Of Paris
Curated by
ChEMBL
Ligand
BDBM50115840
((S)-2-[(S)-2-(5-Bromo-indan-1-yl)-3-mercapto-propi...)
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Copy InChI
Affinity Data
Ki: 3.80nM
Assay Description:
In vitro inhibition of Neutral endopeptidase.
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
Angiotensin-converting enzyme
(Rattus norvegicus)
University Of Paris
Curated by
ChEMBL
Ligand
BDBM50115840
((S)-2-[(S)-2-(5-Bromo-indan-1-yl)-3-mercapto-propi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 4.10nM
Assay Description:
In vitro inhibition of Angiotensin I converting enzyme.
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Neprilysin
(Oryctolagus cuniculus (rabbit))
University Of Paris
Curated by
ChEMBL
Ligand
BDBM50115845
(2-[2-(5-Bromo-indan-1-yl)-3-mercapto-propionylamin...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 5nM
Assay Description:
In vitro inhibition of Neutral endopeptidase.
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
Neprilysin
(Oryctolagus cuniculus (rabbit))
University Of Paris
Curated by
ChEMBL
Ligand
BDBM50115851
((S)-2-[(S)-2-((S)-5-Bromo-indan-1-yl)-3-mercapto-p...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 9.40nM
Assay Description:
In vitro inhibition of Neutral endopeptidase.
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
Angiotensin-converting enzyme
(Rattus norvegicus)
University Of Paris
Curated by
ChEMBL
Ligand
BDBM50115845
(2-[2-(5-Bromo-indan-1-yl)-3-mercapto-propionylamin...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 12nM
Assay Description:
In vitro inhibition of Angiotensin I converting enzyme.
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Neprilysin
(Oryctolagus cuniculus (rabbit))
University Of Paris
Curated by
ChEMBL
Ligand
BDBM50115847
((2S)-2-[(2R)-2-[(1S)-5-bromo-2,3-dihydro-1H-inden-...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 13nM
Assay Description:
In vitro inhibition of Neutral endopeptidase.
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
Endothelin-converting enzyme 1
(Homo sapiens (Human))
University Of Paris
Curated by
ChEMBL
Ligand
BDBM50115843
((2S)-2-[(2R)-2-[(1R)-5-bromo-2,3-dihydro-1H-inden-...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 18nM
Assay Description:
In vitro inhibition of endothelin converting enzyme.
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
UniProtKB/SwissProt
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
EEF1AKMT4-ECE2 readthrough transcript protein
(Homo sapiens (Human))
Pharmaleads
Ligand
BDBM92502
((2S)-2-[2-(5-bromo-2,3-dihydro-1H-inden-1-yl)-3-su...)
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Affinity Data
Ki: 22.3nM IC50: 43.4nM
Assay Description:
Inhibitory assay against ECE-2.
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
Ligand Info
PC cid
PC sid
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Endothelin-converting enzyme 1
(Homo sapiens (Human))
University Of Paris
Curated by
ChEMBL
Ligand
BDBM50115840
((S)-2-[(S)-2-(5-Bromo-indan-1-yl)-3-mercapto-propi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 28nM
Assay Description:
In vitro inhibition of endothelin converting enzyme.
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
UniProtKB/SwissProt
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Endothelin-converting enzyme 1
(Homo sapiens (Human))
University Of Paris
Curated by
ChEMBL
Ligand
BDBM50115845
(2-[2-(5-Bromo-indan-1-yl)-3-mercapto-propionylamin...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 31nM
Assay Description:
In vitro inhibition of endothelin converting enzyme.
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
UniProtKB/SwissProt
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Angiotensin-converting enzyme
(Rattus norvegicus)
University Of Paris
Curated by
ChEMBL
Ligand
BDBM50115843
((2S)-2-[(2R)-2-[(1R)-5-bromo-2,3-dihydro-1H-inden-...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 55nM
Assay Description:
In vitro inhibition of Angiotensin I converting enzyme.
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Angiotensin-converting enzyme
(Rattus norvegicus)
University Of Paris
Curated by
ChEMBL
Ligand
BDBM50115851
((S)-2-[(S)-2-((S)-5-Bromo-indan-1-yl)-3-mercapto-p...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 58nM
Assay Description:
In vitro inhibition of Angiotensin I converting enzyme.
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Angiotensin-converting enzyme
(Rattus norvegicus)
University Of Paris
Curated by
ChEMBL
Ligand
BDBM50115847
((2S)-2-[(2R)-2-[(1S)-5-bromo-2,3-dihydro-1H-inden-...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 66nM
Assay Description:
In vitro inhibition of Angiotensin I converting enzyme.
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Endothelin-converting enzyme 1
(Homo sapiens (Human))
University Of Paris
Curated by
ChEMBL
Ligand
BDBM50115847
((2S)-2-[(2R)-2-[(1S)-5-bromo-2,3-dihydro-1H-inden-...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 90nM
Assay Description:
In vitro inhibition of endothelin converting enzyme.
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
UniProtKB/SwissProt
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Endothelin-converting enzyme 1
(Homo sapiens (Human))
University Of Paris
Curated by
ChEMBL
Ligand
BDBM50115851
((S)-2-[(S)-2-((S)-5-Bromo-indan-1-yl)-3-mercapto-p...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 110nM
Assay Description:
In vitro inhibition of endothelin converting enzyme.
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
UniProtKB/SwissProt
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI