null

SMILES COc1cc(F)ccc1-c1cncc(CNC(C)C)c1

InChI Key InChIKey=GVQRMCLPLPTJNW-UHFFFAOYSA-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 = 50344255   

TargetGlutamate receptor ionotropic, NMDA 2B(Rattus norvegicus (Rat))
AstraZeneca Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50344255(CHEMBL1779008 | N-((5-(4-fluoro-2-methoxyphenyl)py...)copy SMILEScopy InChI
Affinity DataKi:  266nMAssay Description:Displacement of [3H]CP101606 from NR2B in rat brain minus cerebellum membraneMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29887BKPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
AstraZeneca Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50344255(CHEMBL1779008 | N-((5-(4-fluoro-2-methoxyphenyl)py...)copy SMILEScopy InChI
Affinity DataIC50: 6.67E+3nMAssay Description:Inhibition of human ERG expressed in CHOK1 cells electrophysiology studyMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29887BKPubMed