BDBM50029341 8-Chloro-3-(4-dimethylamino-butyl)-5-phenyl-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-ol::CHEMBL114375

SMILES CN(C)CCCCN1CCc2cc(Cl)c(O)cc2C(C1)c1ccccc1

InChI Key InChIKey=JMLZYVMMUDKHMM-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 = 50029341   

TargetD(1A) dopamine receptor(RAT)
National Institutes Of Health

Curated by ChEMBL
LigandPNGBDBM50029341(8-Chloro-3-(4-dimethylamino-butyl)-5-phenyl-2,3,4,...)
Affinity DataKi:  811nMAssay Description:Affinity for Dopamine receptor D1 binding measured by competition against [3H]-SCH- 23390 to rat striatal membraneMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(1A) dopamine receptor(RAT)
National Institutes Of Health

Curated by ChEMBL
LigandPNGBDBM50029341(8-Chloro-3-(4-dimethylamino-butyl)-5-phenyl-2,3,4,...)
Affinity DataKi:  811nMAssay Description:Binding affinity against dopamine receptor D1 from rat striatal membranes using [3H]-SCH- 23390 as radioligand.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Rattus norvegicus (rat))
National Institutes Of Health

Curated by ChEMBL
LigandPNGBDBM50029341(8-Chloro-3-(4-dimethylamino-butyl)-5-phenyl-2,3,4,...)
Affinity DataKi:  3.45E+3nMAssay Description:Affinity for Dopamine receptor D2 binding measured by sulpiride 23390 to rat striatal membraneMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Rattus norvegicus (rat))
National Institutes Of Health

Curated by ChEMBL
LigandPNGBDBM50029341(8-Chloro-3-(4-dimethylamino-butyl)-5-phenyl-2,3,4,...)
Affinity DataKi:  4.13E+3nMAssay Description:Binding affinity against Dopamine receptor D2 from rat striatal membranes, using [3H]sulpiride as radioligand.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed