null

SMILES CC(C)(N)C(=O)N[C@H](Cc1c[nH]c2ccccc12)c1nnc(CCCc2c[nH]c3ccccc23)n1CCc1ccccc1

InChI Key InChIKey=QDIDJSJXSMBMFE-WJOKGBTCSA-N

  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 = 50208646   

TargetGrowth hormone secretagogue receptor type 1(Homo sapiens (Human))
CNRS-Universités Montpellier I et II

Curated by ChEMBL
LigandPNGBDBM50208646((R)-N-(1-(5-(3-(1H-indol-3-yl)propyl)-4-phenethyl-...)copy SMILEScopy InChI
Affinity DataEC50:  15nMAssay Description:Agonist activity at human GHS1a receptor expressed in CHO cells assessed as induction of intracellular calcium mobilizationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2251HW6PubMed
TargetGrowth hormone secretagogue receptor type 1(Homo sapiens (Human))
CNRS-Universités Montpellier I et II

Curated by ChEMBL
LigandPNGBDBM50208646((R)-N-(1-(5-(3-(1H-indol-3-yl)propyl)-4-phenethyl-...)copy SMILEScopy InChI
Affinity DataIC50: 11nMAssay Description:Displacement of [125I-His9]ghrelin from human GHS1a receptor expressed in LLC PK1 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2251HW6PubMed