Home
About
Info
Download
WebServices
Contact
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
11
hits in this display
Target
Angiotensin-converting enzyme
(Homo sapiens (Human))
Cea
Curated by
ChEMBL
Ligand
BDBM50303320
((S)-2-[(R)-3-[((R)-1-Benzyloxycarbonylamino-2-phen...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 0.650nM
Assay Description:
Inhibition of human somatic ACE C-terminal domain
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
MMDB
PC cid
PC sid
PDB
Similars
In Depth
Details
Article
PubMed
PDB
3D Structure (crystal)
Copy BDB DOI
Target
Angiotensin-converting enzyme
(Homo sapiens (Human))
Cea
Curated by
ChEMBL
Ligand
BDBM50303320
((S)-2-[(R)-3-[((R)-1-Benzyloxycarbonylamino-2-phen...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 0.650nM
Assay Description:
Inhibition of human ACE C-terminal domain expressed in CHO cells after 90 mins by fluorescence 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
MMDB
PC cid
PC sid
PDB
Similars
In Depth
Details
Article
PubMed
PDB
3D Structure (crystal)
Copy BDB DOI
Target
Angiotensin-converting enzyme
(Homo sapiens (Human))
Cea
Curated by
ChEMBL
Ligand
BDBM50303320
((S)-2-[(R)-3-[((R)-1-Benzyloxycarbonylamino-2-phen...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 0.680nM
Assay Description:
Inhibition of human somatic ACE in presence of buffer
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
MMDB
PC cid
PC sid
PDB
Similars
In Depth
Details
Article
PubMed
PDB
3D Structure (crystal)
Copy BDB DOI
Target
Angiotensin-converting enzyme
(Homo sapiens (Human))
Cea
Curated by
ChEMBL
Ligand
BDBM50303320
((S)-2-[(R)-3-[((R)-1-Benzyloxycarbonylamino-2-phen...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 4nM
Assay Description:
Inhibition of human somatic ACE in presence of 1:100 diluted SHR rat plasma
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
MMDB
PC cid
PC sid
PDB
Similars
In Depth
Details
Article
PubMed
PDB
3D Structure (crystal)
Copy BDB DOI
Target
Angiotensin-converting enzyme
(Homo sapiens (Human))
Cea
Curated by
ChEMBL
Ligand
BDBM50303320
((S)-2-[(R)-3-[((R)-1-Benzyloxycarbonylamino-2-phen...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 8nM
Assay Description:
Inhibition of human somatic ACE in presence of 1:50 diluted SHR rat plasma
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
MMDB
PC cid
PC sid
PDB
Similars
In Depth
Details
Article
PubMed
PDB
3D Structure (crystal)
Copy BDB DOI
Target
Endothelin-converting enzyme 1
(Homo sapiens (Human))
Cea
Curated by
ChEMBL
Ligand
BDBM50303320
((S)-2-[(R)-3-[((R)-1-Benzyloxycarbonylamino-2-phen...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 14nM
Assay Description:
Inhibition of human somatic ECE1
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
UniProtKB/SwissProt
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
MMDB
PC cid
PC sid
PDB
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Angiotensin-converting enzyme
(Homo sapiens (Human))
Cea
Curated by
ChEMBL
Ligand
BDBM50303320
((S)-2-[(R)-3-[((R)-1-Benzyloxycarbonylamino-2-phen...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 20nM
Assay Description:
Inhibition of human somatic ACE in presence of 1:100 diluted SHR rat plasma complemented with 5 uM serum albumin
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
MMDB
PC cid
PC sid
PDB
Similars
In Depth
Details
Article
PubMed
PDB
3D Structure (crystal)
Copy BDB DOI
Target
Angiotensin-converting enzyme
(Homo sapiens (Human))
Cea
Curated by
ChEMBL
Ligand
BDBM50303320
((S)-2-[(R)-3-[((R)-1-Benzyloxycarbonylamino-2-phen...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 150nM
Assay Description:
Inhibition of human ACE N-terminal domain expressed in CHO cells after 90 mins by fluorescence 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
MMDB
PC cid
PC sid
PDB
Similars
In Depth
Details
Article
PubMed
PDB
3D Structure (crystal)
Copy BDB DOI
Target
Collagenase 3
(Homo sapiens (Human))
Cea
Curated by
ChEMBL
Ligand
BDBM50303320
((S)-2-[(R)-3-[((R)-1-Benzyloxycarbonylamino-2-phen...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 4.00E+3nM
Assay Description:
Inhibition of human MMP13
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
MMDB
PC cid
PC sid
PDB
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Neprilysin
(Homo sapiens (Human))
Cea
Curated by
ChEMBL
Ligand
BDBM50303320
((S)-2-[(R)-3-[((R)-1-Benzyloxycarbonylamino-2-phen...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 6.70E+3nM
Assay Description:
Inhibition of human somatic NEP
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
MMDB
PC cid
PC sid
PDB
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Neprilysin
(Homo sapiens (Human))
Cea
Curated by
ChEMBL
Ligand
BDBM50303320
((S)-2-[(R)-3-[((R)-1-Benzyloxycarbonylamino-2-phen...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 6.70E+3nM
Assay Description:
Inhibition of NEP
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
MMDB
PC cid
PC sid
PDB
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI