BDBM50130715 4-[(Hydroxy-phenethyl-phosphinoylmethyl)-amino]-butyric acid::CHEMBL114552

SMILES OC(=O)CCCN=CP(O)(O)CCc1ccccc1

InChI Key InChIKey=SAEGSBZKLAFBGI-UHFFFAOYSA-N

Data  3 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50130715   

TargetAngiotensin-converting enzyme(Rat)
Institute of Biomedical Chemistry of Russian Academy of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50130715(4-[(Hydroxy-phenethyl-phosphinoylmethyl)-amino]-bu...)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibitory activity against Angiotensin I converting enzyme (ACE) from rat cortex brain membraneMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/27/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Human)
Institute of Biomedical Chemistry of Russian Academy of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50130715(4-[(Hydroxy-phenethyl-phosphinoylmethyl)-amino]-bu...)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibitory activity against Angiotensin I converting enzyme (ACE) from human blood serumMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/27/2012
Entry Details Article
PubMed
TargetNeprilysin(Rat)
Institute of Biomedical Chemistry of Russian Academy of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50130715(4-[(Hydroxy-phenethyl-phosphinoylmethyl)-amino]-bu...)
Affinity DataIC50: 2.00E+6nMAssay Description:Inhibitory activity against neutral endopeptidase (NEP) from rat cortex brain membraneMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/27/2012
Entry Details Article
PubMed