null

SMILES COc1ccc(Cn2c(nnc2C(Cc2c[nH]c3ccccc23)NC(=O)C2CCNCC2)C(Cc2c[nH]c3ccccc23)NC(=O)C(CC(C)C)NC(=O)C(CC(C)C)NC(C)=O)cc1

InChI Key InChIKey=WDNCTAOENIQVSW-GXCFJHMPSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50165587   

TargetGrowth hormone secretagogue receptor type 1(Homo sapiens (Human))
Universit£ de Montpellier

Curated by ChEMBL
LigandPNGBDBM50165587(CHEMBL3800298)copy SMILEScopy InChI
Affinity DataKi:  2nM ΔG°:  -11.9kcal/moleT: 2°CAssay Description:Competitive binding affinity to human SNAP-tagged GHS-R1a expressed in HEK293T cells incubated at 4 degC for 3 hrs or at room temperature for 1 hr by...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J9688VPubMed
TargetGrowth hormone secretagogue receptor type 1(Homo sapiens (Human))
Universit£ de Montpellier

Curated by ChEMBL
LigandPNGBDBM50165587(CHEMBL3800298)copy SMILEScopy InChI
Affinity DataEC50:  4.40nMAssay Description:Agonist activity at human GHS-R1a expressed in HEK293T cells after 45 mins by HTRF-based IP3 turnover assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J9688VPubMed