BDBM50074324 1,5-Bis-(4-chloro-phenyl)-4-methyl-1H-pyrazole-3-carboxylic acid piperidin-1-ylamide::CHEMBL36250

SMILES Cc1c(nn(c1-c1ccc(Cl)cc1)-c1ccc(Cl)cc1)C(=O)NN1CCCCC1

InChI Key InChIKey=JDFAIQMMRYUITC-UHFFFAOYSA-N

Data  5 KI

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50074324   

TargetCannabinoid receptor 1(Rattus norvegicus (rat))
University Of South Carolina

Curated by ChEMBL
LigandPNGBDBM50074324(1,5-Bis-(4-chloro-phenyl)-4-methyl-1H-pyrazole-3-c...)
Affinity DataKi:  55nMAssay Description:Inhibition of [3H]-CP-55,940 binding to cannabinoid receptor 1 in rat brain membranes.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))TBA
LigandPNGBDBM50074324(1,5-Bis-(4-chloro-phenyl)-4-methyl-1H-pyrazole-3-c...)
Affinity DataKi:  60nMAssay Description:Antagonist activity at CB1 receptor (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
TargetCannabinoid receptor 1(Homo sapiens (Human))TBA
LigandPNGBDBM50074324(1,5-Bis-(4-chloro-phenyl)-4-methyl-1H-pyrazole-3-c...)
Affinity DataKi:  60nMAssay Description:Antagonist activity at CB1 receptor (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
TargetCannabinoid receptor 1(Rattus norvegicus (rat))
University Of South Carolina

Curated by ChEMBL
LigandPNGBDBM50074324(1,5-Bis-(4-chloro-phenyl)-4-methyl-1H-pyrazole-3-c...)
Affinity DataKi:  60.4nMAssay Description:Binding affinity against Cannabinoid receptor 1 in rat forebrainMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(MOUSE)
University Of Connecticut

Curated by ChEMBL
LigandPNGBDBM50074324(1,5-Bis-(4-chloro-phenyl)-4-methyl-1H-pyrazole-3-c...)
Affinity DataKi:  836nMAssay Description:Binding affinity against Cannabinoid receptor 2 in mouse spleenMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed