BDBM50380887 CHEMBL2019083

SMILES CCCCn1c2CCCCCCc2cc(C(=O)NC2(CCCCC2)C(O)=O)c1=O

InChI Key InChIKey=JJXMAMRNQTUEMS-UHFFFAOYSA-N

Data  2 KI  2 IC50

  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 = 50380887   

TargetCannabinoid receptor 2(Homo sapiens (Human))
Shionogi

Curated by ChEMBL
LigandPNGBDBM50380887(CHEMBL2019083)
Affinity DataKi:  56nMAssay Description:Displacement of [3H]-CP55940 from human recombinant CB2 receptor after 60 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
Shionogi

Curated by ChEMBL
LigandPNGBDBM50380887(CHEMBL2019083)
Affinity DataKi: >5.00E+3nMAssay Description:Displacement of [3H]-CP55940 from human recombinant CB1 receptor after 60 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Shionogi

Curated by ChEMBL
LigandPNGBDBM50380887(CHEMBL2019083)
Affinity DataIC50:  7nMAssay Description:Agonist activity at human CB2 receptor expressed in CHO cells assessed as inhibition of forskolin-induced cAMP release after 45 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
Shionogi

Curated by ChEMBL
LigandPNGBDBM50380887(CHEMBL2019083)
Affinity DataIC50: >2.00E+3nMAssay Description:Agonist activity at human CB1 receptor expressed in CHO cells assessed as inhibition of forskolin-induced cAMP release after 25 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed