null

SMILES CN(C)c1cncc2sc3c(ncn(-c4ccc(C)cc4)c3=O)c12

InChI Key InChIKey=LPWKFUVWWQYLOD-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 = 50177062   

TargetMetabotropic glutamate receptor 5(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50177062(9-dimethylamino-3-(4-methylphenyl)-3H-5-thia-1,3,7...)copy SMILEScopy InChI
Affinity DataIC50: 4.04E+3nMAssay Description:Antagonist activity at human mGluR5 expressed in 1321N1 cells assessed as effect on L-glutamate-induced calcium mobilizationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27P8XX0PubMed
TargetMetabotropic glutamate receptor 1(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50177062(9-dimethylamino-3-(4-methylphenyl)-3H-5-thia-1,3,7...)copy SMILEScopy InChI
Affinity DataIC50: 43nMAssay Description:Antagonist activity at human mGluR1 expressed in 1321N1 cells assessed as effect on L-glutamate-induced calcium mobilizationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27P8XX0PubMed