Pharmacological Potential of Peruvian <i>Eustephia</i> Species (Amaryllidaceae): Alkaloid Diversity, Cholinesterase Inhibition, and Anti-<i>Trypanosoma cruzi</i> Activity. [PDF]
Llalla-Cordova O +10 more
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Potential Antiviral Compounds from <i>Hippeastrum puniceum</i> Bulb Against Yellow Fever Virus: Bioassay-Guided Fractionation and <i>In Silico</i> Pharmacokinetic Analysis. [PDF]
Flores-Souza E +11 more
europepmc +1 more source
Alkaloid Profile of Fifteen Different Species of <i>Narcissus</i> L. (Amaryllidoideae) Collected in Spain. [PDF]
Rodríguez-Escobar ML +7 more
europepmc +1 more source
Direct evidence for poison use on microlithic arrowheads in Southern Africa at 60,000 years ago. [PDF]
Isaksson S, Högberg A, Lombard M.
europepmc +1 more source
Sustainable Extraction of Alkaloids from <i>Worsleya procera</i>: Improving the Method with Green Chemistry. [PDF]
Duque Rodrigues W +5 more
europepmc +1 more source
Machine Learning-Based QSAR Screening of Colombian Medicinal Flora for Potential Antiviral Compounds Against Dengue Virus: An In Silico Drug Discovery Approach. [PDF]
Montenegro-Herrera SA +4 more
europepmc +1 more source
Haemanthidine-Containing Alkaloid Fraction from <i>Crinum scabrum</i> as a Natural Therapeutics for Chagas Disease. [PDF]
Pardo JB +7 more
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Alkaloids from Narcissus angustifolius subsp. transcarpathicus (Amaryllidaceae)
Phytochemistry, 2002Seven alkaloids have been isolated from fresh bulbs of Narcissus angustifolius subsp. transcarpathicus (Amaryllidaceae). Nangustine, reported here for the first time, is the first 5,11-methanomorphanthridine alkaloid with a C-3/C-4 substitution. The structure and stereochemistry of this new alkaloid, as well as those previously known, have been ...
Machocho, Alex K. +6 more
openaire +4 more sources
Abstract On the basis of the conformations and the established absolute configurations of lycorine (I) and dihdyrolycorine (IX), discussions on quaternization of the alkaloids permit the assignment of the absolute configurations of lycorine α- and β-methiodide, (II and III), and dihydrolycorine methiodide (X), respectively.
K. Kotera, Y. Hamada, R. Nakane
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Amaryllidaceae andSceletiumalkaloids
Natural Product Reports, 2019Recent progress on the isolation, identification, biological activity and synthetic studies of Amaryllidaceae alkaloids, as well as the structurally close alkaloids from theSceletiumgenus, published from July 2015 to June 2017 are reviewed.
Zhong Jin, Guangmin Yao
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