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• W2066601618 abstract "A series of hybrid molecules, by reacting berberine with benzenediol, melatonin, or ferulic acid, were designed and synthesized. These compounds were evaluated for: (i) the ability to inhibit multiple cholinesterases (ChEs); (ii) the capacity to prevent amyloid β (Aβ) aggregation; and (iii) antioxidant potential. We designed and synthesized a series of hybrid molecules, in an effort to identify novel multifunctional drug candidates for Alzheimer’s disease (AD), by reacting berberine with benzenediol, melatonin, and ferulic acid. The products were evaluated for: (i) the ability to inhibit multiple cholinesterases (ChEs); (ii) the capacity to prevent amyloid β (Aβ) aggregation; and (iii) antioxidant activity. All of the derivatives were better antioxidants, and inhibited Aβ aggregation to a greater extent, than the lead compound, berberine. Two of the hybrids, in particular, have the potential to be excellent candidates for AD therapy: the berberine-pyrocatechol hybrid (compound 8 ) was a much better inhibitor of acetylcholinesterase (AChE) than unconjugated berberine (IC 50 : 0.123 vs 0.374 μM); and the berberine-hydroquinone hybrid (compound 12 ) displayed high antioxidant activity, could inhibit AChE (IC 50 of 0.460 μM), and had the greatest ability to inhibit Aβ aggregation." @default.
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• W2066601618 date "2011-12-01" @default.
• W2066601618 modified "2023-09-23" @default.
• W2066601618 title "Benzenediol-berberine hybrids: Multifunctional agents for Alzheimer’s disease" @default.
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• W2066601618 doi "https://doi.org/10.1016/j.bmc.2011.09.040" @default.
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