BDBM50331290 CHEMBL1289953::N-(3-aminopropyl)-2-(3-methylbenzyloxy)-N-(thiophen-2-ylmethyl)benzamide
SMILES Cc1cccc(COc2ccccc2C(=O)N(CCCN)Cc2cccs2)c1
InChI Key InChIKey=LCQJRANJHOEQFG-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 4 hits for monomerid = 50331290
TargetTransient receptor potential cation channel subfamily M member 8(Homo sapiens (Human))
Kissei Pharmaceutical
Curated by ChEMBL
Kissei Pharmaceutical
Curated by ChEMBL
Affinity DataIC50: 414nMAssay Description:Antagonist activity at human recombinant TRPM8 expressed in HEK293 cells assessed as inhibition of menthol-induced calcium increase by Fluo-4 AM base...More data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily M member 8(Homo sapiens (Human))
Kissei Pharmaceutical
Curated by ChEMBL
Kissei Pharmaceutical
Curated by ChEMBL
Affinity DataIC50: 589nMAssay Description:Antagonist activity at human recombinant full length TRPM8 expressed in HEK293 cells assessed as inhibition of icilin-induced calcium increase preinc...More data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily M member 8(Homo sapiens (Human))
Kissei Pharmaceutical
Curated by ChEMBL
Kissei Pharmaceutical
Curated by ChEMBL
Affinity DataIC50: 447nMAssay Description:Antagonist activity at human recombinant TRPM8 expressed in HEK293 cells assessed as inhibition of icilin-induced calcium increase by Fluo-4 AM based...More data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily M member 8(Homo sapiens (Human))
Kissei Pharmaceutical
Curated by ChEMBL
Kissei Pharmaceutical
Curated by ChEMBL
Affinity DataIC50: 448nMAssay Description:Antagonist activity at human recombinant TRPM8 expressed in HEK293 cells assessed as inhibition of icilin-induced calcium increase by Fluo-4 AM based...More data for this Ligand-Target Pair