null

SMILES COc1ccc(OC[C@@H]2N(CCc3cc(OC(C)C)ccc23)C(=O)c2cccc(Cl)c2)cc1

InChI Key InChIKey=JLDCFMMLFCEFCP-SANMLTNESA-N

  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 2 hits for monomerid = 50238359   

TargetGlutamate receptor ionotropic, NMDA 1/2D(RAT)
Emory University

Curated by ChEMBL
LigandPNGBDBM50238359(CHEMBL4091772)copy SMILEScopy InChI
Affinity DataEC50:  1.00E+3nMAssay Description:Positive allosteric modulation of recombinant rat GluN1/GluN2D receptor expressed in xenopus laevis oocyte assessed as potentiation of glutamate and ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q298898HPubMed
TargetGlutamate receptor ionotropic, NMDA 1/2C(RAT)
Emory University

Curated by ChEMBL
LigandPNGBDBM50238359(CHEMBL4091772)copy SMILEScopy InChI
Affinity DataEC50:  710nMAssay Description:Positive allosteric modulation of recombinant rat GluN1/GluN2C receptor expressed in xenopus laevis oocyte assessed as potentiation of glutamate and ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q298898HPubMed