null

SMILES Clc1cc2OCOc2cc1CN1CCC2(CC1)N(CNC2=O)c1ccccc1

InChI Key InChIKey=QATNQFJQXRFOHL-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 10 hits for monomerid = 50105072   

TargetDelta-type opioid receptor(Homo sapiens (Human))
F-59000 Lille

Curated by ChEMBL
LigandPNGBDBM50105072(8-(6-Chloro-benzo[1,3]dioxol-5-ylmethyl)-1-phenyl-...)copy SMILEScopy InChI
Affinity DataIC50: 138nMAssay Description:Inhibition of ligand binding to human delta opioid receptor.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2057GN9PubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
F-59000 Lille

Curated by ChEMBL
LigandPNGBDBM50105072(8-(6-Chloro-benzo[1,3]dioxol-5-ylmethyl)-1-phenyl-...)copy SMILEScopy InChI
Affinity DataIC50: 138nMAssay Description:Binding affinity against delta-opiate receptor (human) using [3H]-DPDPE radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q23X87B8PubMed
LigandPNGBDBM50105072(8-(6-Chloro-benzo[1,3]dioxol-5-ylmethyl)-1-phenyl-...)copy SMILEScopy InChI
Affinity DataIC50: 1.11E+3nMAssay Description:Binding affinity against L-type calcium channel verapamil siteMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2057GN9PubMed
TargetKappa-type opioid receptor(Homo sapiens (Human))
F-59000 Lille

Curated by ChEMBL
LigandPNGBDBM50105072(8-(6-Chloro-benzo[1,3]dioxol-5-ylmethyl)-1-phenyl-...)copy SMILEScopy InChI
Affinity DataIC50: 5.70nMAssay Description:Binding affinity against opioid receptor kappa 1 using [3H]- U-69,593 radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q23X87B8PubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
F-59000 Lille

Curated by ChEMBL
LigandPNGBDBM50105072(8-(6-Chloro-benzo[1,3]dioxol-5-ylmethyl)-1-phenyl-...)copy SMILEScopy InChI
Affinity DataIC50: 581nMAssay Description:Inhibition of sigma receptorMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2057GN9PubMed
TargetNociceptin receptor(Homo sapiens (Human))
F-59000 Lille

Curated by ChEMBL
LigandPNGBDBM50105072(8-(6-Chloro-benzo[1,3]dioxol-5-ylmethyl)-1-phenyl-...)copy SMILEScopy InChI
Affinity DataIC50: 97nMAssay Description:Inhibition of human ORL1 orphanin receptorMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2057GN9PubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
F-59000 Lille

Curated by ChEMBL
LigandPNGBDBM50105072(8-(6-Chloro-benzo[1,3]dioxol-5-ylmethyl)-1-phenyl-...)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Binding affinity against mu opiate receptorMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2057GN9PubMed
TargetD(3) dopamine receptor(Homo sapiens (Human))
F-59000 Lille

Curated by ChEMBL
LigandPNGBDBM50105072(8-(6-Chloro-benzo[1,3]dioxol-5-ylmethyl)-1-phenyl-...)copy SMILEScopy InChI
Affinity DataIC50: 2.12E+3nMAssay Description:Inhibition of human dopamine receptor D3More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2057GN9PubMed
TargetKappa-type opioid receptor(Homo sapiens (Human))
F-59000 Lille

Curated by ChEMBL
LigandPNGBDBM50105072(8-(6-Chloro-benzo[1,3]dioxol-5-ylmethyl)-1-phenyl-...)copy SMILEScopy InChI
Affinity DataIC50: 5.70nMAssay Description:Binding affinity against opioid receptor kappa 1 by using [3H]U-69593 as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2057GN9PubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
F-59000 Lille

Curated by ChEMBL
LigandPNGBDBM50105072(8-(6-Chloro-benzo[1,3]dioxol-5-ylmethyl)-1-phenyl-...)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Binding affinity against mu-opiate receptor (human) using [3H]DAMGO radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q23X87B8PubMed