BDBM50073805 3-((4-(4-chlorophenyl)piperazin-1-yl)methyl)H-pyrazolo[1,5-a]pyridine::3-[4-(4-Chloro-phenyl)-piperazin-1-ylmethyl]-pyrazolo[1,5-a]pyridine::4-(4-Chloro-phenyl)-1-pyrazolo[1,5-a]pyridin-3-ylmethyl-piperazin-1-ium::CHEMBL7927::FAUC 113

SMILES Clc1ccc(cc1)N1CCN(Cc2cnn3ccccc23)CC1

InChI Key InChIKey=XVPRVMIFXXOEFR-UHFFFAOYSA-N

Data  41 KI  2 EC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50073805   

TargetD(4) dopamine receptor(Homo sapiens (Human))
Universit£T Erlangen-N£Rnberg

Curated by ChEMBL
LigandPNGBDBM50073805(3-((4-(4-chlorophenyl)piperazin-1-yl)methyl)H-pyra...)
Affinity DataKi:  2nMAssay Description:Binding affinity evaluated for the displacement of [3H]spiperone against human dopamine receptor D4More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(BOVINE)
Universit£T Erlangen-N£Rnberg

Curated by ChEMBL
LigandPNGBDBM50073805(3-((4-(4-chlorophenyl)piperazin-1-yl)methyl)H-pyra...)
Affinity DataKi:  4.70E+3nMAssay Description:Binding affinity was evaluated for the displacement of [3H]spiperone against bovine Dopamine receptor D2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(3) dopamine receptor(Homo sapiens (Human))
Universit£T Erlangen-N£Rnberg

Curated by ChEMBL
LigandPNGBDBM50073805(3-((4-(4-chlorophenyl)piperazin-1-yl)methyl)H-pyra...)
Affinity DataKi:  5.00E+3nMAssay Description:Binding affinity evaluated for the displacement of [3H]-spiperone against human dopamine receptor D3More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(1A) dopamine receptor(BOVINE)
Universit£T Erlangen-N£Rnberg

Curated by ChEMBL
LigandPNGBDBM50073805(3-((4-(4-chlorophenyl)piperazin-1-yl)methyl)H-pyra...)
Affinity DataKi:  1.20E+4nMAssay Description:Binding affinity was evaluated for the displacement of [3H]-SCH- 23390 against bovine Dopamine receptor D1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed