Acetylcholinesterase Inhibition and Antioxidant Activity of --Caffeoyldopamine and --Feruloyldopamine.

Phenolic acids and their derivatives found in nature are well-known for their potential biological activity. In this study, two amides derived from -caffeic/ferulic acid and dopamine were synthesized and characterized by Fourier-transform infrared spectroscopy (FTIR), mass spectrometry, proton and carbon-13 nuclear magnetic resonance spectroscopy. The compounds were tested for the inhibition of acetylcholinesterase (AChE) from and for antioxidant activity by scavenging 2,2-diphenyl-1-pycrylhydrazyl free radical (DPPH) and 2,2′-azinobis(3-ethylbenzothiazoline-6-sulphonic acid) radical cation (ABTS), reducing ferric ions, and ferrous ions chelation. --Feruloyldopamine displayed the highest inhibitory effect on AChE with half-maximal inhibitory concentration () values of 8.52 μM. In addition, an in silico study was done to determine the most favorable AChE cluster with the synthesized compounds. Further, these clusters were investigated for binding positions at the lowest free binding energy. Both synthesized hydroxycinnamates were found to be better antioxidants than the parent acids in in vitro tests applied. --Caffeoyldopamine showed the best antioxidant activity in the three tested methods—against non-biological stable free radicals 5.95 μM for DPPH, 0.24 μM for the ABTS method, and for reducing power (ascorbic acid equivalent 822.45 μmol/mmol)—while for chelation activity against Fe ions --feruloyldopamine had slightly better antioxidant activity ( 3.17 mM).