null

SMILES O=S(=O)(Cc1ccc2CCNCCc2c1)c1ccc(nc1)N1CCOCC1

InChI Key InChIKey=JHFOAJJQKIXOJU-UHFFFAOYSA-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 3 hits for monomerid = 50311426   

TargetCytochrome P450 2D6(Homo sapiens (Human))
GlaxoSmithKline

Curated by ChEMBL
LigandPNGBDBM50311426(4-(5-((2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-yl)m...)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+4nMAssay Description:Inhibition of human recombinant CYP2D6More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DV1K0CPubMed
TargetMotilin receptor(Homo sapiens (Human))
GlaxoSmithKline

Curated by ChEMBL
LigandPNGBDBM50311426(4-(5-((2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-yl)m...)copy SMILEScopy InChI
Affinity DataEC50:  501nMAssay Description:Agonist activity at human recombinant motilin receptor expressed in CHO cells by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DV1K0CPubMed
TargetGrowth hormone secretagogue receptor type 1(Homo sapiens (Human))
GlaxoSmithKline

Curated by ChEMBL
LigandPNGBDBM50311426(4-(5-((2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-yl)m...)copy SMILEScopy InChI
Affinity DataEC50: >1.00E+3nMAssay Description:Agonist activity at human gherlin receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DV1K0CPubMed