BDBM50391281 CHEMBL5286642

SMILES OCc1ccccc1-c1ccc(CO[C@H]2CC[C@@H]([C@H]2OC\C=C/CCC(O)=O)N2CCCCCC2)cc1

InChI Key InChIKey=KCLYPNKWGQYJSE-LYFCCYKMSA-N

Data  2 IC50  1 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 3 hits for monomerid = 50391281   

Target5-hydroxytryptamine receptor 4(Homo sapiens (Human))TBA
LigandPNGBDBM50391281(CHEMBL5286642)
Affinity DataEC50:  24nMAssay Description:Antagonist potency against carbachol induced contractions of isolated guinea pig ileum Muscarinic acetylcholine receptorMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))TBA
LigandPNGBDBM50391281(CHEMBL5286642)
Affinity DataIC50:  1.39E+4nMAssay Description:The compound was tested for beta-adrenergic activity against Beta-1 adrenergic receptor from guinea pig right atriaMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))TBA
LigandPNGBDBM50391281(CHEMBL5286642)
Affinity DataIC50:  1.12E+4nMAssay Description:Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
In DepthDetails PubMed