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BDBM50044226 1-hydroxy-1-phenylethyl-phosphinoylamino]-propionyl-pyrrolidine-2-carboxylic acid::CHEMBL62955::Compound 16

SMILES: CC(NP(O)(=O)CCc1ccccc1)C(=O)N1CCCC1C(O)=O

InChI Key: InChIKey=VUEMZVPEAVUVHY-UHFFFAOYSA-N

Data: 2 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50044226   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Angiotensin-converting enzyme


(Homo sapiens (Human))
BDBM50044226
PNG
(1-hydroxy-1-phenylethyl-phosphinoylamino]-propiony...)
Show SMILES CC(NP(O)(=O)CCc1ccccc1)C(=O)N1CCCC1C(O)=O
Show InChI InChI=1S/C16H23N2O5P/c1-12(15(19)18-10-5-8-14(18)16(20)21)17-24(22,23)11-9-13-6-3-2-4-7-13/h2-4,6-7,12,14H,5,8-11H2,1H3,(H,20,21)(H2,17,22,23)
PDB
MMDB

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KEGG

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CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 25.1n/an/an/an/an/an/a



University of Michigan

Curated by ChEMBL


Assay Description
Inhibition of angiotensin I converting enzyme in silico


J Med Chem 40: 3161-72 (1997)


Article DOI: 10.1021/jm970211n
BindingDB Entry DOI: 10.7270/Q2MG7QPB
More data for this
Ligand-Target Pair
Thermolysin


(Bacillus thermoproteolyticus)
BDBM50044226
PNG
(1-hydroxy-1-phenylethyl-phosphinoylamino]-propiony...)
Show SMILES CC(NP(O)(=O)CCc1ccccc1)C(=O)N1CCCC1C(O)=O
Show InChI InChI=1S/C16H23N2O5P/c1-12(15(19)18-10-5-8-14(18)16(20)21)17-24(22,23)11-9-13-6-3-2-4-7-13/h2-4,6-7,12,14H,5,8-11H2,1H3,(H,20,21)(H2,17,22,23)
PDB
MMDB

B.MOAD
DrugBank
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
n/an/a 7n/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of metallopeptidase thermolysin


J Med Chem 36: 2051-8 (1993)


BindingDB Entry DOI: 10.7270/Q2NP2524
More data for this
Ligand-Target Pair