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Recent progress on biological activity of amaryllidaceae and further isoquinoline alkaloids in connection with alzheimer's disease

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The present review demonstrates that, during the last decade, a number of AAs and IAs have been isolated and tested against various targets connected with the po tential treatment of AD. Two new structural types of AAs have been isolated, identified and screened for biological activity connected with AD. Compounds of the carltonine-type have been identified as strong selective inhibitors of BuChE, and compounds of the narcikachnine-type showed inhibitory activity against both cholinesterases. Several IAs have been identified as multitarget ligands for AD. Moreover, some of the active compounds have also been investigated through molecular docking studies to identify the sites of interaction between the chemical scaffold and the enzymatic amino acid residues. (7.918Mb)
Date
2021-08-29
Author
Wijaya, Viriyanata
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Abstract
Alzheimer’s disease (AD) is a progressive age-related neurodegenerative disease recognized as the most common form of dementia among elderly people. Due to the fact that the exact pathogenesis of AD still remains to be fully elucidated, the treatment is only symptomatic and available drugs are not able to modify AD progression. Considering the increase in life expectancy worldwide, AD rates are predicted to increase enormously, and thus the search for new AD drugs is urgently needed. Due to their complex nitrogen-containing structures, alkaloids are considered to be promising candidates for use in the treatment of AD. Since the introduction of galanthamine as an antidementia drug in 2001, Amaryllidaceae alkaloids (AAs) and further isoquinoline alkaloids (IAs) have been one of the most studied groups of alkaloids. In the last few years, several compounds of new structure types have been isolated and evaluated for their biological activity connected with AD. The present review aims to comprehensively summarize recent progress on AAs and IAs since 2010 up to June 2021 as potential drugs for the treatment of AD.
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http://repository.unmul.ac.id/handle/123456789/51811
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Repository Universitas Mulawarman copyright ©   LP3M Universitas Mulawarman
Jalan Kuaro Kotak Pos 1068
Telp. (0541) 741118
Fax. (0541) 747479 - 732870
Samarinda 75119, Kalimantan Timur, Indonesia
Contact Us | Send Feedback