BDBM50341511 CHEMBL1765632::N-(4-(4-Phenylbenzoylamino)butyl)-N-propyl-4-amino-4,5-dihydro-3H-pyrazolo[4,5,1-i,j]quinoline

SMILES CCCN(CCCCNC(=O)c1ccc(cc1)-c1ccccc1)C1Cc2cnn3cccc(C1)c23

InChI Key InChIKey=LQCUFDIAPSFACZ-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 = 50341511   

TargetD(3) dopamine receptor(Homo sapiens (Human))
Friedrich-Alexander University

Curated by ChEMBL
LigandPNGBDBM50341511(CHEMBL1765632 | N-(4-(4-Phenylbenzoylamino)butyl)-...)
Affinity DataKi:  0.550nMAssay Description:Displacement of [3H]spiperone from human dopamine D3 receptor expressed in CHO cells after 60 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Homo sapiens (Human))
Friedrich-Alexander University

Curated by ChEMBL
LigandPNGBDBM50341511(CHEMBL1765632 | N-(4-(4-Phenylbenzoylamino)butyl)-...)
Affinity DataKi:  240nMAssay Description:Displacement of [3H]spiperone from human dopamine D2short receptor expressed in CHO cells after 60 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Homo sapiens (Human))
Friedrich-Alexander University

Curated by ChEMBL
LigandPNGBDBM50341511(CHEMBL1765632 | N-(4-(4-Phenylbenzoylamino)butyl)-...)
Affinity DataKi:  270nMAssay Description:Displacement of [3H]spiperone from human dopamine D2long receptor expressed in CHO cells after 60 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(1A) dopamine receptor(Sus scrofa)
Friedrich-Alexander University

Curated by ChEMBL
LigandPNGBDBM50341511(CHEMBL1765632 | N-(4-(4-Phenylbenzoylamino)butyl)-...)
Affinity DataKi:  1.80E+3nMAssay Description:Displacement of [3H]SCH23390 from dopamine D1 receptor in porcine cerebral cortex after 60 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed