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Updated: Feb 6, 2026

Detection of Histone Modifications in Plant Leaves
Published on: September 23, 2011
Withanolides from the leaves of Datura metel L
Rui Guo1, Yan Liu2, Zhen-Peng Xu2
1Shanxi Key Laboratory of Innovative Drug for the Treatment of Serious Diseases Basing on the Chronic Inflammation, Shanxi University of Chinese Medicine, Jinzhong, 030619, China.
Abstract:
Twelve previously undescribed withanolides, including three uncommon chemotypes of aglycones, daturafolisides (J-L), and six common structures, daturafolisides (M-U), as well as one known withanolide were isolated from the leaves of Datura metel L. Their structures were elucidated by interpretation of spectroscopic data (1D, 2D NMR and CD), HRESIMS experiments and comparison with published data for similar compounds. These isolated compounds were evaluated for their inhibitory activities on nitric oxide production. The IC50 values of daturafoliside L, daturafoliside M, and daturafoliside T were between 9.37 and 18.64 μM, while daturafoliside K, daturafoliside R, and daturametelin A had IC50 values of 22.83-33.36 μM. Herein, three proposed biosynthetic pathways for uncommon structures daturafolisides J-L were discussed. These constituents found in the leaves of Datura metel L. may be a good source of bioactive substances, making contributions to the sustainable utilization of this plant resources.
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Leaving Groups
In general, in a nucleophilic substitution reaction, a nucleophile displaces a functional group, called the leaving group, from the substrate to give a substituted product. A leaving group departs the substrate molecule through heterolytic cleavage, taking the pair of electrons with it to become a relatively stable weak base in the form of an anion or a neutral molecule.
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