BDBM50220833 5-(5-propyl-1H-pyrazol-3-yl)-1H-tetrazole::CHEMBL393064

SMILES CCCc1cc(n[nH]1)-c1nnn[nH]1

InChI Key InChIKey=FQGVBFKPIPPKKG-UHFFFAOYSA-N

Data  4 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 = 50220833   

TargetHydroxycarboxylic acid receptor 2(Homo sapiens (Human))
Arena Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50220833(5-(5-propyl-1H-pyrazol-3-yl)-1H-tetrazole | CHEMBL...)
Affinity DataEC50:  7.76E+3nMAssay Description:Agonist activity at human GPR109a expressed in human adipocytes assessed as decrease in intracellular cAMP level by HTRF assayChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHydroxycarboxylic acid receptor 3(Homo sapiens (Human))
Arena Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50220833(5-(5-propyl-1H-pyrazol-3-yl)-1H-tetrazole | CHEMBL...)
Affinity DataEC50:  724nMAssay Description:Agonist activity at human GPR109b expressed in human adipocytes assessed as decrease in intracellular cAMP level by HTRF assayChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHydroxycarboxylic acid receptor 2(Homo sapiens (Human))
Arena Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50220833(5-(5-propyl-1H-pyrazol-3-yl)-1H-tetrazole | CHEMBL...)
Affinity DataEC50:  7.76E+3nMAssay Description:Agonist activity at human GPR109a expressed in human adipocytes assessed as decrease in intracellular cAMP level by HTRF assayChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHydroxycarboxylic acid receptor 3(Homo sapiens (Human))
Arena Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50220833(5-(5-propyl-1H-pyrazol-3-yl)-1H-tetrazole | CHEMBL...)
Affinity DataEC50:  724nMAssay Description:Agonist activity at human GPR109b expressed in human adipocytes assessed as decrease in intracellular cAMP level by HTRF assayChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed