BDBM50341509 CHEMBL1765630::N-(4-(4-Phenylbenzoylamino)butyl)-N-propyl-5-amino-3-chloro-4,5,6,7-tetrahydropyrazolo[1,5-a]pyridine

SMILES CCCN(CCCCNC(=O)c1ccc(cc1)-c1ccccc1)C1CCn2ncc(Cl)c2C1

InChI Key InChIKey=DJUWRNXEJLCKJK-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 = 50341509   

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

Curated by ChEMBL
LigandPNGBDBM50341509(CHEMBL1765630 | N-(4-(4-Phenylbenzoylamino)butyl)-...)
Affinity DataKi:  0.590nMAssay 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
LigandPNGBDBM50341509(CHEMBL1765630 | N-(4-(4-Phenylbenzoylamino)butyl)-...)
Affinity DataKi:  43nMAssay 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
LigandPNGBDBM50341509(CHEMBL1765630 | N-(4-(4-Phenylbenzoylamino)butyl)-...)
Affinity DataKi:  100nMAssay 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
LigandPNGBDBM50341509(CHEMBL1765630 | N-(4-(4-Phenylbenzoylamino)butyl)-...)
Affinity DataKi:  3.60E+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