Institute of Natural Medicine and Health Products, School of Pharmaceutical Sciences, Zhejiang Provincial Key Laboratory of Plant Evolutionary Ecology and Conservation, Taizhou University, Zhejiang, 318000, China; School of Pharmacy, Fudan University, Shanghai, 201203, China.
Institute of Natural Medicine and Health Products, School of Pharmaceutical Sciences, Zhejiang Provincial Key Laboratory of Plant Evolutionary Ecology and Conservation, Taizhou University, Zhejiang, 318000, China.
Phytochemistry. 2024 Dec;228:114259. doi: 10.1016/j.phytochem.2024.114259. Epub 2024 Aug 24.
A comprehensive phytochemical investigation of the flower buds and leaves/twigs of Heptacodium miconioides, a cultivated ornamental plant native to China and categorized as 'vulnerable', has led to the isolation of 45 structurally diverse compounds, which comprise 18 phenylpropanoids (1-4, 7-20), 11 pentacyclic triterpenoids (5, 6, 21-29), eight secoiridoid glycosides (30-37), three quinic acid derivatives (38-40), and a few miscellaneous components (41-45). Among them, (+)-α-intermedianol (1), (+)-holophyllol A (2), and (-)-pseudolarkaemin A (3) represent previously unreported enantiomeric lignans, while (+)-7'(R)-hydroxymatairesinol (4) is an undescribed naturally occurring lignan. Heptacoacids A (5) and B (6) are undescribed 24-nor-urs-28-oic acid derivatives. Their chemical structures were determined by 2D-NMR, supplemented by evidence from specific rotations and circular dichroism spectra. Given the uncertainty surrounding the systematic position of Heptacodium, integrative taxonomy (ITA), a method utilized to define contentious species, is applied. Chemotaxonomy, a vital aspect of ITA, becomes significant. By employing hierarchical clustering analysis (HCA) and syntenic pattern analysis methods, a taxonomic examination based on the major specialized natural products from the flower buds of H. miconioides and two other Caprifoliaceae plants (i.e., Lonicera japonica and Abelia × grandiflora) could offer enhanced understanding of the systematic placement of Heptacodium. Additionally, compounds 39 and 40 displayed remarkable inhibitory activities against ATP-citrate lyase (ACL), with IC values of 0.11 and 1.10 μM, respectively. In summary, the discovery of medical properties and refining systematic classification can establish a sturdy groundwork for conservation efforts aimed at mitigating species diversity loss while addressing human diseases.
对中国原产的栽培观赏植物、被列为“易危”的六道木的花蕾和叶/小枝进行了全面的植物化学研究,从中分离得到了 45 种结构多样的化合物,包括 18 种苯丙素(1-4、7-20)、11 种五环三萜(5、6、21-29)、8 种裂环环烯醚萜苷(30-37)、3 种奎宁酸衍生物(38-40)和一些其他成分(41-45)。其中,(+)-α-中脂素(1)、(+)-霍朴酚 A(2)和(-)-假拉卡敏 A(3)代表以前未报道过的对映体木脂素,而(+)-7'(R)-羟基马替瑞林(4)是一种未描述的天然存在的木脂素。Heptacoacids A(5)和 B(6)是未描述的 24-降乌苏-28-酸衍生物。它们的化学结构通过 2D-NMR 确定,并辅以比旋光度和圆二色光谱的证据。由于六道木的系统位置不确定,因此应用整合分类学(ITA),一种用于定义有争议物种的方法。化学分类学是 ITA 的一个重要方面。通过运用层次聚类分析(HCA)和同基因模式分析方法,基于六道木花蕾和两种其他忍冬科植物(即金银花和杂种长春花)的主要特化天然产物进行分类学检查,可以更好地理解六道木的系统位置。此外,化合物 39 和 40 对 ATP-柠檬酸裂解酶(ACL)显示出显著的抑制活性,IC 值分别为 0.11 和 1.10 μM。综上所述,发现医疗特性和完善系统分类可以为保护工作奠定坚实的基础,以减轻物种多样性的丧失,同时解决人类疾病问题。