BDBM50380892 CHEMBL2019090::S-777469

SMILES CCc1c(C)cc(C(=O)NC2(CCCCC2)C(O)=O)c(=O)n1Cc1ccc(F)cc1

InChI Key InChIKey=JIYXOJFSPOFZPY-UHFFFAOYSA-N

Data  6 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 = 50380892   

TargetCannabinoid receptor 1(Homo sapiens (Human))
Shionogi

Curated by ChEMBL
LigandPNGBDBM50380892(CHEMBL2019090 | S-777469)
Affinity DataKi:  4.07E+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 1(Homo sapiens (Human))
Shionogi

Curated by ChEMBL
LigandPNGBDBM50380892(CHEMBL2019090 | S-777469)
Affinity DataKi:  4.60E+3nMAssay Description:Agonist activity at CB1 receptor (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
Shionogi

Curated by ChEMBL
LigandPNGBDBM50380892(CHEMBL2019090 | S-777469)
Affinity DataKi:  4.61E+3nMAssay Description:Agonist activity at human CB1 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
Shionogi

Curated by ChEMBL
LigandPNGBDBM50380892(CHEMBL2019090 | S-777469)
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