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BDBM50416470 CHEMBL1209646

SMILES: C[C@H]1CN(C[C@@H](C)N1)C(=O)c1cn2[C@@H](COc3cccc1c23)C1CCCCC1

InChI Key: InChIKey=ZTLQGTKQJAZKOK-YRNRMSPPSA-N

Data: 1 EC50

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   Substructure
Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50416470   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50416470
PNG
(CHEMBL1209646)
Show SMILES C[C@H]1CN(C[C@@H](C)N1)C(=O)c1cn2[C@@H](COc3cccc1c23)C1CCCCC1 |r|
Show InChI InChI=1S/C23H31N3O2/c1-15-11-25(12-16(2)24-15)23(27)19-13-26-20(17-7-4-3-5-8-17)14-28-21-10-6-9-18(19)22(21)26/h6,9-10,13,15-17,20,24H,3-5,7-8,11-12,14H2,1-2H3/t15-,16+,20-/m0/s1
PDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 126n/an/an/an/a



Schering-Plough Research Institute

Curated by ChEMBL


Assay Description
Agonist activity at human cannabinoid CB1 receptor expressed in CHO cells after 5 hrs by luciferase reporter gene assay


Bioorg Med Chem Lett 20: 4918-21 (2010)


Article DOI: 10.1016/j.bmcl.2010.06.067
BindingDB Entry DOI: 10.7270/Q21R6RS6
More data for this
Ligand-Target Pair