null

SMILES CN1CC(c2ccccc2Cl)c2ccc(OCCCN3CCC(F)CC3)cc2C1

InChI Key InChIKey=FLLOSWVXSHXQDY-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 3 hits for monomerid = 50199596   

TargetHistamine H3 receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research and Development L.L.C.

Curated by ChEMBL
LigandPNGBDBM50199596(4-(2-chlorophenyl)-7-(3-(4-fluoropiperidin-1-yl)pr...)copy SMILEScopy InChI
Affinity DataKi:  5.60nMAssay Description:Binding affinity at human histamine H3 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4BXBPubMed
TargetSodium-dependent serotonin transporter(Rattus norvegicus (rat))
Johnson & Johnson Pharmaceutical Research and Development L.L.C.

Curated by ChEMBL
LigandPNGBDBM50199596(4-(2-chlorophenyl)-7-(3-(4-fluoropiperidin-1-yl)pr...)copy SMILEScopy InChI
Affinity DataKi:  17nMAssay Description:Binding affinity at rat SERTMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4BXBPubMed
TargetSodium-dependent serotonin transporter(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research and Development L.L.C.

Curated by ChEMBL
LigandPNGBDBM50199596(4-(2-chlorophenyl)-7-(3-(4-fluoropiperidin-1-yl)pr...)copy SMILEScopy InChI
Affinity DataKi:  18nMAssay Description:Binding affinity at human SERTMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4BXBPubMed