BDBM50046625 1R,2R-trans-2-[(Benzoyloxycarbamoyl-methyl)-carbamoyl]-cyclohexanecarboxylic acid::1R,2S-cis-2-[(Benzoyloxycarbamoyl-methyl)-methyl-carbamoyl]-cyclohexanecarboxylic acid::1S,2R-cis-2-[(Benzoyloxycarbamoyl-methyl)-methyl-carbamoyl]-cyclohexanecarboxylic acid::1S,2S-trans-2-[(Benzoyloxycarbamoyl-methyl)-carbamoyl]-cyclohexanecarboxylic acid::CHEMBL351655

SMILES CN(CC(=O)NOC(=O)c1ccccc1)C(=O)[C@@H]1CCCC[C@@H]1C(O)=O

InChI Key InChIKey=CEPGXHKYSQTFIP-UHFFFAOYSA-N

Data  2 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50046625   

TargetAngiotensin-converting enzyme(Rat)
Laboratori Guidotti

Curated by ChEMBL
LigandPNGBDBM50046625(1S,2R-cis-2-[(Benzoyloxycarbamoyl-methyl)-methyl-c...)
Affinity DataIC50: 1.50E+5nMAssay Description:In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/26/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
Laboratori Guidotti

Curated by ChEMBL
LigandPNGBDBM50046625(1S,2R-cis-2-[(Benzoyloxycarbamoyl-methyl)-methyl-c...)
Affinity DataIC50: 1.50E+5nMAssay Description:In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/26/2012
Entry Details Article
PubMed