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Chirality
Article . 2017 . Peer-reviewed
License: Wiley Online Library User Agreement
Data sources: Crossref
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
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Chirality
Article . 2018
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Amaryllidaceae alkaloids: Absolute configuration and biological activity

Authors: Alessio Cimmino; Marco Masi; Marco Evidente; Stefano Superchi; Antonio Evidente;

Amaryllidaceae alkaloids: Absolute configuration and biological activity

Abstract

AbstractPlants belonging to the Amaryllidaceae family are well known for their ornamental and medicinal use. Plant members of this group are distributed through both tropical and subtropical regions of the world and are dominant in Andean South America, the Mediterranean basin, and southern Africa. Amaryllidaceae plants have been demonstrated to be a good source of alkaloids with a large spectrum of biological activities, the latter being strictly related to the absolute stereochemistry of the alkaloid scaffold. Among them, great importance for practical applications in medicine has galanthamine, which has already spawned an Alzheimer's prescription drug as a potent and selective inhibitor of the enzyme acetylcholinesterase. Furthermore, lycorine as well as its related isocarbostyryl analogs narciclasine and pancratistatine have shown a strong anticancer activity in vitro against different solid tumors with malignant prognosis. This review addresses the assignment of the absolute configuration of several Amaryllidaceae alkaloids and its relationship with their biological activities.

Country
Italy
Keywords

Pharmacology, structure-activity relationship, Drug Discovery3003 Pharmaceutical Science, Amaryllidaceae, structure-activity relationships, Organic Chemistry, Pharmaceutical Science, alkaloids; Amaryllidaceae; biological activity; relative and/or absolute configuration; structure-activity relationships; Analytical Chemistry; Catalysis; Pharmacology; Drug Discovery3003 Pharmaceutical Science; Spectroscopy; Organic Chemistry, biological activity, Stereoisomerism, alkaloid, alkaloids, Catalysis, Catalysi, Analytical Chemistry, Structure-Activity Relationship, Drug Discovery, Amaryllidaceae Alkaloids, relative and/or absolute configuration, Spectroscopy

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
64
Top 10%
Top 10%
Top 10%
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