null

SMILES Clc1ccccc1-c1cc(on1)-c1cnn(c1)C1CCNCC1

InChI Key InChIKey=ZYSDUCLOQUOUSW-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50264883   

TargetNeuronal acetylcholine receptor subunit alpha-4(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50264883(3-(2-chlorophenyl)-5-(1-(piperidin-4-yl)-1H-pyrazo...)copy SMILEScopy InChI
Affinity DataEC50:  120nMAssay Description:Activation of human alpha4beta2 nAChR assessed as potentiation of submaximal response to nicotine induced currentMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6D26PubMed
TargetNeuronal acetylcholine receptor subunit alpha-3(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50264883(3-(2-chlorophenyl)-5-(1-(piperidin-4-yl)-1H-pyrazo...)copy SMILEScopy InChI
Affinity DataEC50: >1.00E+5nMAssay Description:Activation of human alpha3beta4 nAChR assessed as potentiation of submaximal response to nicotine induced currentMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6D26PubMed
TargetNeuronal acetylcholine receptor subunit alpha-3(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50264883(3-(2-chlorophenyl)-5-(1-(piperidin-4-yl)-1H-pyrazo...)copy SMILEScopy InChI
Affinity DataEC50: >1.00E+5nMAssay Description:Activation of human alpha3beta2 nAChR assessed as potentiation of submaximal response to nicotine induced currentMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6D26PubMed