Structure–activity relationship on human serum paraoxonase (PON1) using substrate analogues and inhibitors

Structure–activity relationship on human serum paraoxonase (PON1) using substrate analogues and inhibitors Paraoxon, 4-nitrophenyl phosphate and acetate are substrates of α- but not of β-, γ- and ζ-carbonic anhydrases Phosphonate analogs of pyridoxal phosphate with shortened side chains Synthesis and anti-acetylcholinesterase properties of novel β- and γ-substituted alkoxy organophosphonates Anticholinesterase Activity of Compounds Related to Geneserine Tautomers. N-Oxides and 1,2-Oxazines Probes of the active site of norepinephrine N-methyltransferase: effect of hydrophobic and hydrophilic interactions on side-chain binding of amphetamine and .alpha.-methylbenzylamine Conformational requirements of substrates for activity with phenylethanolamine N-methyltransferase Catechol O-methyltransferase. 8. Structure-activity relationships for inhibition by 8-hydroxyquinolines The structure-activity relationships of a series of suicide inhibitors of phospholipase A2 Methyl Analogues of the Experimental Alzheimer Drug Phenserine:  Synthesis and Structure/Activity Relationships for Acetyl- and Butyrylcholinesterase Inhibitory Action