BDBM50102350 3-(4-(2-methoxyphenyl)piperazin-1-yl)-1-(5-methylthiophen-2-yl)propan-1-one::3-[4-(2-Methoxy-phenyl)-piperazin-1-yl]-1-(5-methyl-thiophen-2-yl)-propan-1-one::CHEMBL137591

SMILES COc1ccccc1N1CCN(CCC(=O)c2ccc(C)s2)CC1

InChI Key InChIKey=GKFAMQWFMFWCRS-UHFFFAOYSA-N

Data  4 KI

  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 4 hits for monomerid = 50102350   

Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
Universidade Federal Da Para£Ba

Curated by ChEMBL
LigandPNGBDBM50102350(3-(4-(2-methoxyphenyl)piperazin-1-yl)-1-(5-methylt...)
Affinity DataKi:  17.4nMAssay Description:Antagonist activity at 5HT1AMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
Universidade Federal Da Para£Ba

Curated by ChEMBL
LigandPNGBDBM50102350(3-(4-(2-methoxyphenyl)piperazin-1-yl)-1-(5-methylt...)
Affinity DataKi:  17.4nMAssay Description:Binding affinity to 5HT1A receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Rattus norvegicus (rat))
Universidad De Navarra

Curated by ChEMBL
LigandPNGBDBM50102350(3-(4-(2-methoxyphenyl)piperazin-1-yl)-1-(5-methylt...)
Affinity DataKi:  17.5nMAssay Description:Binding affinity to 5-hydroxytryptamine 1A receptor (5-HT 1A receptor, serotonin receptor) from rat cortex using [3H]-8-OH-DPAT as radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSodium-dependent serotonin transporter(Rattus norvegicus (rat))
Universidad De Navarra

Curated by ChEMBL
LigandPNGBDBM50102350(3-(4-(2-methoxyphenyl)piperazin-1-yl)-1-(5-methylt...)
Affinity DataKi: >5.00E+3nMAssay Description:Binding affinity towards Serotonin transporter from rat cortex measured using [3H]-paroxetineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed