BDBM50527969 CHEMBL4462603

SMILES CC(=O)N[C@@H](CC(O)=O)C(=O)NC[C@H](CC1(CCCC1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(O)=O)C(O)=O

InChI Key InChIKey=ZQIWHIVXBQEYTN-UHFFFAOYSA-N

Data  2 KI

PDB links: 3 PDB IDs match this monomer.

  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 = 50527969   

TargetAngiotensin-converting enzyme(Human)
University of Bath

Curated by ChEMBL
LigandPNGBDBM50527969(CHEMBL4462603)
Affinity DataKi:  7.40E+3nMAssay Description:Inhibition of human testis ACE C-domain lacking unique O-glycosylated region, transmembrane anchor and cytoplasmic tail expressed in CHO cells using ...More data for this Ligand-Target Pair
In DepthDetails Article
PubMedPDB3D3D Structure (crystal)
TargetAngiotensin-converting enzyme(Human)
University of Bath

Curated by ChEMBL
LigandPNGBDBM50527969(CHEMBL4462603)
Affinity DataKi:  1.06E+4nMAssay Description:Inhibition of human somatic ACE N-domain soluble form (1 to 629 residues) expressed in CHO cells using Z-FHL as substrate preincubated with enzyme fo...More data for this Ligand-Target Pair
In DepthDetails Article
PubMedPDB3D3D Structure (crystal)