null

SMILES CCCCNC(=O)CCn1nnnc1[C@@H](COCc1ccccc1)NC(=O)C(C)(C)N

InChI Key InChIKey=JIYGGZBKPXFOMQ-QGZVFWFLSA-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 = 50222165   

TargetGrowth hormone secretagogue receptor type 1(Homo sapiens (Human))
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50222165(2-amino-N-{(S)-2-benzyloxy-1-[1-(2-butylcarbamoyl-...)copy SMILEScopy InChI
Affinity DataKi:  2.19E+3nMAssay Description:Displacement of [125I]Ghrelin from human GHSR1a after 1 hrMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28P607DPubMed
TargetGrowth hormone secretagogue receptor type 1(Homo sapiens (Human))
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50222165(2-amino-N-{(S)-2-benzyloxy-1-[1-(2-butylcarbamoyl-...)copy SMILEScopy InChI
Affinity DataEC50:  42nMAssay Description:Agonist activity at human GHS receptor expressed in H4 glioma cells assessed as intracellular calcium concentration by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28P607DPubMed