null

SMILES Fc1ccc(CCOCc2nc3ncccc3c(=O)[nH]2)cc1

InChI Key InChIKey=AJRBNFYXHNKFTP-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 5 hits for monomerid = 50325922   

TargetHydroxycarboxylic acid receptor 2(Homo sapiens (Human))
F. Hoffmann-La Roche Ltd

Curated by ChEMBL
LigandPNGBDBM50325922(2-((4-fluorophenethyloxy)methyl)pyrido[2,3-d]pyrim...)copy SMILEScopy InChI
Affinity DataIC50: 630nMAssay Description:Displacement of radioligand from human GPR109AMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NV9JGFPubMed
TargetHydroxycarboxylic acid receptor 3(Homo sapiens (Human))
F. Hoffmann-La Roche Ltd

Curated by ChEMBL
LigandPNGBDBM50325922(2-((4-fluorophenethyloxy)methyl)pyrido[2,3-d]pyrim...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Displacement of radioligand from human GPR109BMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NV9JGFPubMed
TargetHydroxycarboxylic acid receptor 2(Rattus norvegicus)
F. Hoffmann-La Roche Ltd

Curated by ChEMBL
LigandPNGBDBM50325922(2-((4-fluorophenethyloxy)methyl)pyrido[2,3-d]pyrim...)copy SMILEScopy InChI
Affinity DataIC50: 2.70E+3nMAssay Description:Displacement of radioligand from rat GPR109AMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NV9JGFPubMed
TargetHydroxycarboxylic acid receptor 2(Homo sapiens (Human))
F. Hoffmann-La Roche Ltd

Curated by ChEMBL
LigandPNGBDBM50325922(2-((4-fluorophenethyloxy)methyl)pyrido[2,3-d]pyrim...)copy SMILEScopy InChI
Affinity DataEC50:  2.50E+3nMAssay Description:Agonist activity at human GPR109A receptor assessed as GTPgammaS bindingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NV9JGFPubMed
TargetHydroxycarboxylic acid receptor 2(Rattus norvegicus)
F. Hoffmann-La Roche Ltd

Curated by ChEMBL
LigandPNGBDBM50325922(2-((4-fluorophenethyloxy)methyl)pyrido[2,3-d]pyrim...)copy SMILEScopy InChI
Affinity DataEC50:  1.60E+3nMAssay Description:Agonist activity at rat GPR109A receptor assessed as GTPgammaS bindingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NV9JGFPubMed