null

SMILES CNS(=O)(=O)Cc1ccccc1-c1ccc(COC2CC[C@@H]([C@H]2OC\C=C/CCC(O)=O)N2CCCCCC2)cc1

InChI Key InChIKey=BPXWFRXHKNVENH-UCXNPNORSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50391287   

LigandPNGBDBM50391287(CHEMBL5278176)copy SMILEScopy InChI
Affinity DataIC50: 1.40E+3nMAssay Description:Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
In DepthDetails
Target5-hydroxytryptamine receptor 4(Homo sapiens (Human))TBA
LigandPNGBDBM50391287(CHEMBL5278176)copy SMILEScopy InChI
Affinity DataEC50:  59nMAssay Description:Antagonist potency against carbachol induced contractions of isolated guinea pig ileum Muscarinic acetylcholine receptorMore data for this Ligand-Target Pair
In DepthDetails