BDBM50010480 CHEMBL3264008

SMILES CN[C@@H](C(C)C)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1ccc(O)cc1)P(O)(O)=O

InChI Key InChIKey=AFAFFSSNAUKMNO-HBMCJLEFSA-N

Data  3 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 3 hits for monomerid = 50010480   

TargetAngiotensin-converting enzyme(Oryctolagus cuniculus)
Vanderbilt University Department Of Chemistry

Curated by ChEMBL
LigandPNGBDBM50010480(CHEMBL3264008)
Affinity DataIC50:  140nMAssay Description:Inhibition of rabbit lung somatic ACE using FAPGG substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Homo sapiens (Human))
Vanderbilt University Department Of Chemistry

Curated by ChEMBL
LigandPNGBDBM50010480(CHEMBL3264008)
Affinity DataIC50:  54nMAssay Description:Inhibition of human ACE N-terminal domain using Cbz-Phe-His-Leu-OH substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Homo sapiens (Human))
Vanderbilt University Department Of Chemistry

Curated by ChEMBL
LigandPNGBDBM50010480(CHEMBL3264008)
Affinity DataIC50:  52nMAssay Description:Inhibition of human ACE C-terminal domain using Cbz-Phe-His-Leu-OH substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed