BDBM50392283 CHEMBL2153670

SMILES CC(C)[C@H](N=C(NS(=O)(=O)c1ccc(Cl)cc1)N1C[C@@H](C(=N1)c1ccc(Cl)cc1)c1ccccc1)C(N)=O

InChI Key InChIKey=GTCSIQFTNPTSLO-RPWUZVMVSA-N

Data  4 IC50

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

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50392283   

TargetCannabinoid receptor 2(Homo sapiens (Human))
Jenrin Discovery

Curated by ChEMBL
LigandPNGBDBM50392283(CHEMBL2153670)
Affinity DataIC50: >1.00E+3nMAssay Description:Displacement of 3[H]ligand from recombinant human CB2 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
Jenrin Discovery

Curated by ChEMBL
LigandPNGBDBM50392283(CHEMBL2153670)
Affinity DataIC50:  0.5nMAssay Description:Displacement of 3[H]ligand from recombinant human CB1 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
Jenrin Discovery

Curated by ChEMBL
LigandPNGBDBM50392283(CHEMBL2153670)
Affinity DataIC50:  2nMAssay Description:Displacement of 3[H]ligand from recombinant human CB1 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Jenrin Discovery

Curated by ChEMBL
LigandPNGBDBM50392283(CHEMBL2153670)
Affinity DataIC50: >1.00E+3nMAssay Description:Displacement of 3[H]ligand from recombinant human CB2 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed