BDBM50187331 (R,E)-6-((1-((2-(2-hydroxyethoxy)phenethyl)(methyl)amino)-3-(naphthalen-2-yl)-1-oxopropan-2-yl)(methyl)amino)-N,2-dimethyl-6-oxohex-4-en-2-aminium::5-methyl-5-methylamino-hex-2-enoic acid [(R)-1-({2-[2-(2-hydroxy-ethoxy)-phenyl]-ethyl}-methyl-carbamoyl)-2-naphthalen-2-yl-ethyl]-methyl-amide::CHEMBL376970

SMILES CNC(C)(C)C\C=C\C(=O)N(C)[C@H](Cc1ccc2ccccc2c1)C(=O)N(C)CCc1ccccc1OCCO

InChI Key InChIKey=GYIPHGRIGGSXCL-UHFFFAOYSA-N

Data  2 EC50

  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 = 50187331   

TargetGrowth hormone secretagogue receptor type 1(Human)
University of Milan

Curated by ChEMBL
LigandPNGBDBM50187331((R,E)-6-((1-((2-(2-hydroxyethoxy)phenethyl)(methyl...)
Affinity DataEC50:  5nMAssay Description:Activity at human GHS-R1a receptor in rat pituitary cells assessed as GH releaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/7/2012
Entry Details Article
PubMed
TargetGrowth hormone secretagogue receptor type 1(Human)
University of Milan

Curated by ChEMBL
LigandPNGBDBM50187331((R,E)-6-((1-((2-(2-hydroxyethoxy)phenethyl)(methyl...)
Affinity DataEC50:  5nMAssay Description:Agonist activity at human GHS-R1More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/13/2012
Entry Details Article
PubMed