BDBM50350149 CHEMBL1814312

SMILES COc1ccc(cc1CC=C)-c1cc(CC=C)cc(NC(C)=O)c1O

InChI Key InChIKey=KNYQXFHNRYTONS-UHFFFAOYSA-N

Data  1 KI  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 4 hits for monomerid = 50350149   

LigandPNGBDBM50350149(CHEMBL1814312)
Affinity DataEC50:  5.30E+3nMAssay Description:Allosteric modulation of GABAAalpha1beta2gamma2s receptor (unknown origin) expressed in Xenopus laevis oocytes assessed as potentiation of GABA-induc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/4/2016
Entry Details Article
PubMed
LigandPNGBDBM50350149(CHEMBL1814312)
Affinity DataEC50:  6.81E+4nMAssay Description:Partial agonist activity at GABAAalpha1beta2gamma2s receptor (unknown origin) expressed in Xenopus laevis oocytes assessed as induction of chloride c...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/4/2016
Entry Details Article
PubMed
TargetGamma-aminobutyric acid receptor subunit alpha-1/beta-2(Human)
University of Vienna

Curated by ChEMBL
LigandPNGBDBM50350149(CHEMBL1814312)
Affinity DataEC50:  3.80E+3nMAssay Description:Modulation of GABA Aalpha1beta2 receptor expressed in Xenopus laevis oocytes assessed as potentiation of GABA-induced chloride current at holding pot...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2012
Entry Details Article
PubMed
TargetCannabinoid receptor 2(Human)
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50350149(CHEMBL1814312)
Affinity DataKi: >1.00E+4nMAssay Description:Displacement of [3H]CP55940 from human CB2 receptor expressed in CHO cell membranes after 2 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/19/2017
Entry Details Article
PubMed