Results 31 to 40 of about 2,622 (201)

Cytotoxicity Studies of Amaryllidaceae Alkaloids

open access: yesNatural Product Communications, 2016
The plant family Amaryllidaceae is recognizable for its esthetic floral characteristics, its widespread usage in traditional medicine as well as its unique alkaloid principles.
Jerald J. Nair   +2 more
doaj   +1 more source

A comprehensive review of non-alkaloidal metabolites from the subfamily Amaryllidoideae (Amaryllidaceae)

open access: yesOpen Chemistry, 2023
Amaryllidoideae is a subfamily belonging to the Amaryllidaceae and is widely distributed in the southern hemisphere. The subfamily is well known for its content of pharmacologically active alkaloids and represents an important epicenter of Amaryllidaceae-
Ibrakaw Abobaker S.   +2 more
doaj   +1 more source

Chemical and Biological Aspects of Different Species of the Genus Clinanthus Herb. (Amaryllidaceae) from South America

open access: yesMolecules, 2023
The genus Clinanthus Herb. is found in the Andes Region (South America), mainly in Peru, Ecuador, and Bolivia. These plants belong to the Amaryllidaceae family, specifically the Amaryllidoideae subfamily, which presents an exclusive group of alkaloids ...
María Lenny Rodríguez-Escobar   +7 more
doaj   +1 more source

(Amaryllidaceae) Alkaloids

open access: yes, 2021
The Libellus de Medicinalibus Indorum Herbis (Booklet of Indian Medicinal Plants) is the first book of medicinal plants written in the American continent. It was first published in 1939 as ‘An Aztec Herbal’. One of the depicted plants is Huetzcanixochitl
Jaume Bastida   +11 more
core   +1 more source

Alkaloids of the South African Amaryllidaceae: A Review [PDF]

open access: yesNatural Product Communications, 2013
The plant family Amaryllidaceae is known for its horticultural and ornamental appeal as well as its medicinal value. In relation to these characteristics, trade in Amaryllid flower varieties (especially daffodils) is a multi-million dollar revenue generator for the floriculture industry.
Jerald J, Nair   +4 more
openaire   +2 more sources

Pharmacological and toxicological effects of Amaryllidaceae

open access: yesBrazilian Journal of Biology, 2023
The Amaryllidaceae family is widely distributed in the tropics, presenting biological activity attributed mostly to alkaloids, such as an important inhibitory activity of acetylcholinesterase (AChE), antifungal, antibacterial, and cytotoxic activities ...
M. J. M. Paiva   +4 more
doaj   +1 more source

Chemical Composition and Enzyme Inhibitory Activities of Turkish Bulbs

open access: yesNatural Product Communications, 2019
The chemical composition of the bulbs of Pancratium maritimum L. (Amaryllidaceae) from Turkey (Pamucak, Aydın) has been determined by gas chromatography-mass spectrometry.
Buket Bozkurt   +2 more
doaj   +1 more source

GC/MS Analysis of Three Amaryllidaceae Species and Their Cholinesterase Activity

open access: yesNatural Product Communications, 2011
Alzheimer's disease (AD), characterized by the death of nerve cells in the cerebral cortex, is the most common subtype of dementia. Despite the exponential growth in the number of AD patients, acetylcholinesterase (AChE) inhibitors are currently used to ...
Lucie Cahlíková   +4 more
doaj   +1 more source

An overview on the chemical and biological aspects of lycorine alkaloid [PDF]

open access: yesJournal of Advanced Biomedical and Pharmaceutical Sciences, 2018
Amaryllidaceae plants are currently appreciated as a plentiful source of unique bioactive alkaloids. Among them, lycorine is one of the major pyrrolophenanthridine alkaloids commonly isolated from different species of this family.
Marwa Khalifa   +3 more
doaj   +1 more source

Total synthesis of the Amaryllidaceae alkaloid clivonine [PDF]

open access: yesOrganic & Biomolecular Chemistry, 2011
Two syntheses of the Amaryllidaceae alkaloid clivonine (1) are described. Both employ previously reported 7-arylhydrindane 6 as an intermediate but differ in the method employed for subsequent introduction of what becomes the ring-B lactone carbonyl carbon (C7). The synthesis featuring a Bischler-Napieralski reaction for this transformation constitutes
Haning, H   +8 more
openaire   +4 more sources

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