BDBM50222800 (2-allyl-4-(ethylsulfonyl)-1,2,3,4-tetrahydropyrrolo[3,4-b]indol-7-yl)(4-methylpiperidin-1-yl)methanone::CHEMBL250608

SMILES CCS(=O)(=O)n1c2CN(CC=C)Cc2c2cc(ccc12)C(=O)N1CCC(C)CC1

InChI Key InChIKey=MORUSKYOVHFQPY-UHFFFAOYSA-N

Data  2 KI  1 EC50

  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 3 hits for monomerid = 50222800   

TargetCannabinoid receptor 2(Homo sapiens (Human))
Astrazeneca R&D Montreal

Curated by ChEMBL
LigandPNGBDBM50222800((2-allyl-4-(ethylsulfonyl)-1,2,3,4-tetrahydropyrro...)
Affinity DataKi:  6.40nMAssay Description:Binding affinity to human CB2 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
Astrazeneca R&D Montreal

Curated by ChEMBL
LigandPNGBDBM50222800((2-allyl-4-(ethylsulfonyl)-1,2,3,4-tetrahydropyrro...)
Affinity DataKi:  263nMAssay Description:Binding affinity to human CB1 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Astrazeneca R&D Montreal

Curated by ChEMBL
LigandPNGBDBM50222800((2-allyl-4-(ethylsulfonyl)-1,2,3,4-tetrahydropyrro...)
Affinity DataEC50:  0.300nMAssay Description:Agonist activity at human CB2 receptor by GTPgamma[35S] assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed