BDBM50382748 CHEMBL2023046

SMILES OC(=O)[C@H](NC(=O)c1cc2CCCCCCc2n(CC2CCCCC2)c1=O)c1ccccc1

InChI Key InChIKey=YFPOEFGJMGESDL-UHFFFAOYSA-N

Data  2 KI  2 IC50

  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 = 50382748   

TargetCannabinoid receptor 1(Human)
Shionogi

Curated by ChEMBL
LigandPNGBDBM50382748(CHEMBL2023046)
Affinity DataIC50: 2.00E+3nMAssay Description:Agonist activity at human CB1 receptor expressed in CHO cells assessed as increase in forskolin-induced cAMP levels after 20 minsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/7/2013
Entry Details Article
PubMed
TargetCannabinoid receptor 2(Human)
Shionogi

Curated by ChEMBL
LigandPNGBDBM50382748(CHEMBL2023046)
Affinity DataIC50: 4.40nMAssay Description:Agonist activity at human CB2 receptor expressed in CHO cells assessed as increase in forskolin-induced cAMP levels after 20 minsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/7/2013
Entry Details Article
PubMed
TargetCannabinoid receptor 2(Human)
Shionogi

Curated by ChEMBL
LigandPNGBDBM50382748(CHEMBL2023046)
Affinity DataKi:  3nMAssay Description:Displacement of [3H]CP55940 from human CB2 receptor membrane fractionsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/7/2013
Entry Details Article
PubMed
TargetCannabinoid receptor 1(Human)
Shionogi

Curated by ChEMBL
LigandPNGBDBM50382748(CHEMBL2023046)
Affinity DataKi:  69nMAssay Description:Displacement of [3H]CP55940 from human CB1 receptor membrane fractionsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/7/2013
Entry Details Article
PubMed