BDBM50232669 CHEMBL4079631

SMILES O=Cc1cc2cn(c3cccc(o1)c23)S(=O)(=O)c1cccc2ccccc12

InChI Key InChIKey=AYZRIKBBHZCKTA-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 = 50232669   

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

Curated by ChEMBL
LigandPNGBDBM50232669(CHEMBL4079631)
Affinity DataKi:  266nMAssay Description:Displacement of [3H]-LSD from 5-HT6 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
LigandPNGBDBM50232669(CHEMBL4079631)
Affinity DataKi:  5.16E+3nMAssay 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
LigandPNGBDBM50232669(CHEMBL4079631)
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
Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
Polish Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50232669(CHEMBL4079631)
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