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Monoterpene Indole Alkaloids with Antimicrobial Activity Against <i>Helicobacter pylori</i>. [PDF]
Int J Mol SciMarques AT +9 more
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Tetrahedron, 1968
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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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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Amaryllidaceae and Sceletium alkaloids
Natural Product Reports, 2003The latest progress on the isolation, identification, biological activity and synthetic studies of the structurally diverse alkaloids from plants of family Amaryllidaceae has been summarized in this review.
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Cytotoxic Activity of Amaryllidaceae Alkaloids
Planta Medica, 199525 Amaryllidaceae alkaloids belonging to different skeletal types were evaluated for their cytotoxic activity against one murine non-tumoral cell line (LMTK) and two human tumoral cell lines (Molt4 and HepG2) according to established protocols. Significant differences of activity related with the type of skeleton of the tested alkaloids could be ...
B, Weniger +7 more
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Total Synthesis of Amaryllidaceae Alkaloid Buflavine
The Journal of Organic Chemistry, 2002A concise synthesis of the amaryllidaceae alkaloid buflavine (1) and its regioisomer (2) involving sequential Meyers' biaryl coupling, enecarbamate formation, and hydrogenation followed by ultimate intramolecular reductive amination is presented.
Christophe, Hoarau +3 more
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Apoptosis-Inducing Effects of Amaryllidaceae Alkaloids
Current Medicinal Chemistry, 2016The Amaryllidaceae occupies a privileged status amongst medicinal plants in having delivered the Alzheimer's drug galanthamine to the clinical market. Following its resounding success, there have been several positive indicators for the emergence of an anticancer drug from the family due to the potent antiproliferative activities manifested by several ...
Jerald J, Nair +2 more
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Alkaloid N-oxides of amaryllidaceae
Phytochemistry, 1988Ungiminorine N-oxide was isolated from Pancratium maritimum, and homolycorine N-oxide and O-methyl lycorenine N-oxide from Lapiedra martinezii. These compounds represent the first examples of naturally occurring N-oxides from the Amaryllidaceae. © 1988.
R. Suau +5 more
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Heterocyclic Amaryllidaceae Alkaloids: Biosynthesis and Pharmacological Applications
Current Topics in Medicinal Chemistry, 2016Amaryllidaceae alkaloids (AAs), which are natural heterocyclic compounds, are isolated from Amaryllidaceae plants such as narcissus, snowdrop and spider lily. AAs have been extensively studied due to their multiple pharmacological properties. Nevertheless, knowledge of AA synthesis in plants is lacking and most genes encoding enzymes involved in their ...
Tarun, Hotchandani +1 more
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Chemodiversity, chemotaxonomy and chemoecology of Amaryllidaceae alkaloids
2020The Amaryllidaceae alkaloids are a distinctive chemotaxonomic feature of the subfamily Amaryllidoideae of the family Amaryllidaceae, which consists of 59 genera and >800 species distributed primarily in tropical and subtropical areas. Since the first isolation, ca.
Berkov, Strahil +3 more
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