Synthesis and biological evaluation of O-benzyl-hispidol derivatives and analogs as dual monoamine oxidase-B inhibitors and anti-neuroinflammatory agents.

Design, synthesis, and biological evaluation of two series of O-benzyl-hispidol derivatives and the analogous corresponding O-benzyl derivatives aiming to develop selective monoamine oxidase-B inhibitors endowed with anti-neuroinflammatory activity is reported herein. The first O-benzyl-hispidol derivatives series afforded several more potentially active and MAO-B inhibitors than the O-benzyl derivatives series. The most potential compound 2e of O-benzyl derivatives elicited sub-micromolar MAO-B IC of 0.38 µM with a selectivity index >264 whereas most potential compound 3b of O-benzyl derivatives showed only 0.95 MAO-B IC and a selectivity index >105. Advancement of the most active compounds showing sub-micromolar activities to further cellular evaluations of viability and induced production of pro-neuroinflammatory mediators confirmed compound 2e as a potential lead compound inhibiting the production of the neuroinflammatory mediator nitric oxide significantly by microglial BV2 cells at 3 µM concentration without significant cytotoxicity up to 30 µM. In silico molecular docking study predicted plausible binding modes with MAO enzymes and provided insights at the molecular level. Overall, this report presents compound 2e as a potential lead compound to develop potential multifunctional compounds.