BDBM50232668 CHEMBL4103891

SMILES O=S(=O)(c1cccc2ccccc12)n1cc2cc(oc3cccc1c23)C#N

InChI Key InChIKey=PSFIYMABNVWJEG-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 = 50232668   

Target5-hydroxytryptamine receptor 6(Homo sapiens (Human))
Polish Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50232668(CHEMBL4103891)
Affinity DataKi:  755nMAssay Description:Displacement of [3H]-LSD from 5-HT6 receptor (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
Polish Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50232668(CHEMBL4103891)
Affinity DataKi: >1.00E+4nMAssay Description:Displacement of [3H]-8-OH-DPAT from 5HT1A receptor (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Homo sapiens (Human))
Polish Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50232668(CHEMBL4103891)
Affinity DataKi: >1.00E+4nMAssay Description:Displacement of [3H]-Raclopride from D2L receptor (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 7(Homo sapiens (Human))
Polish Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50232668(CHEMBL4103891)
Affinity DataKi: >1.00E+4nMAssay Description:Displacement of [3H]-5-CT from 5-HT7b receptor (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed