BDBM50017288 CHEMBL3287713::US10099993, Compound 62

SMILES COc1cc(ccc1OCCCCOc1ccc(C(=O)C(C)C)c(O)c1C)C(O)=O

InChI Key InChIKey=FXHWDUICKDQMSQ-UHFFFAOYSA-N

Data  3 EC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50017288   

TargetMetabotropic glutamate receptor 2(Human)
Sanford-Burnham Medical Research Institute

US Patent
LigandPNGBDBM50017288(CHEMBL3287713 | US10099993, Compound 62)
Affinity DataEC50:  113nMpH: 7.3 T: 2°CAssay Description:Human Embryonic Kidney (HEK-293) cell lines co-expressing rat mGlu receptors 2, 3, 4, 6, 7 or 8 and G protein-coupled inwardly-rectifying potassium (...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/18/2019
Entry Details
US Patent

TargetMetabotropic glutamate receptor 2(Human)
Sanford-Burnham Medical Research Institute

US Patent
LigandPNGBDBM50017288(CHEMBL3287713 | US10099993, Compound 62)
Affinity DataEC50:  113nMAssay Description:Positive allosteric modulation of rat mGluR2 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/10/2015
Entry Details Article
PubMed
TargetMetabotropic glutamate receptor 3(Human)
Sanford-Burnham Medical Research Institute

US Patent
LigandPNGBDBM50017288(CHEMBL3287713 | US10099993, Compound 62)
Affinity DataEC50: >3.00E+4nMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/18/2019
Entry Details
US Patent