null

SMILES CC(C)(C)OC(=O)N1CCC(CC1)(c1nccn1Cc1ccccc1)c1ccccc1

InChI Key InChIKey=SVTNFNAXOFWCDX-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50213390   

TargetDelta-type opioid receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50213390(CHEMBL392266 | tert-butyl 4-(1-benzyl-1H-imidazol-...)copy SMILEScopy InChI
Affinity DataKi:  9.30nMAssay Description:Displacement of [3H]DPDPE from cloned human delta opioid receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TT4QMMPubMed
TargetKappa-type opioid receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50213390(CHEMBL392266 | tert-butyl 4-(1-benzyl-1H-imidazol-...)copy SMILEScopy InChI
Affinity DataKi:  84nMAssay Description:Displacement of [3H]U-69593 from cloned human kappa opioid receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TT4QMMPubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50213390(CHEMBL392266 | tert-butyl 4-(1-benzyl-1H-imidazol-...)copy SMILEScopy InChI
Affinity DataKi: >465nMAssay Description:Displacement of [3H]DAMGO from cloned human mu opioid receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TT4QMMPubMed