null

SMILES CC(C)C[C@H](NC(=O)[C@H](C)NC(=O)C[C@H](O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](Cc1ccccc1)NC(=O)OCc1ccccc1)[C@@H](O)CC(O)=O

InChI Key InChIKey=HFNYGDLEULFDOF-HBLAKGRZSA-N

  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 2 hits for monomerid = 50226300   

TargetRenin(Homo sapiens (Human))
SANOFI Recherche

Curated by ChEMBL
LigandPNGBDBM50226300(CHEMBL3142776)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of human plasma reninMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50P7GPubMed
TargetRenin(Homo sapiens (Human))
SANOFI Recherche

Curated by ChEMBL
LigandPNGBDBM50226300(CHEMBL3142776)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:In vitro inhibitory activity against rat plasma reninMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VH5PD3PubMed