State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China.
State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China.
Bioorg Chem. 2019 Oct;91:103113. doi: 10.1016/j.bioorg.2019.103113. Epub 2019 Jul 22.
Five new compounds (1-5), including three hexalactone derivatives (1-3) and a pair of new oxaspiro-carbon epimeric glycosides (4 and 5), and six known compounds (6-11) were obtained from the fruits of Illicium lanceolatum. The structures of the new compounds were elucidated using extensive spectroscopic data. The absolute configurations of compounds 1-3 were determined by an analysis of their CD spectra. It was determined that compounds 4 and 5, which are epimeric at C-5, possess the same 1-oxaspiro[4,5]decane-7α,8α,9β-triol moiety. Plausible biogenetic pathways for 4 and 5 derived from the key precursor shikimic acid were proposed. Compounds 1-11 were all assayed on monosodium glutamate-induced human neuroblastoma SH-SY5Y cell damage. The results demonstrated that compounds 4, 5, and 8-10 possess potential neuroprotective effects. The anti-inflammatory, antiviral, and cytotoxic activities of 1-11 were also evaluated.
从八角茴香果实中分离得到了 5 个新化合物(1-5),包括 3 个六氢内酯衍生物(1-3)和一对新的氧杂螺环碳差向异构体糖苷(4 和 5),以及 6 个已知化合物(6-11)。利用广泛的光谱数据阐明了新化合物的结构。通过分析它们的 CD 光谱确定了化合物 1-3 的绝对构型。确定了在 C-5 处具有差向异构体的化合物 4 和 5 具有相同的 1-氧杂螺[4.5]癸烷-7α,8α,9β-三醇部分。提出了 4 和 5 可能来源于关键前体莽草酸的生物合成途径。对 1-11 进行了谷氨酸单钠诱导的人神经母细胞瘤 SH-SY5Y 细胞损伤的测定。结果表明,化合物 4、5 和 8-10 具有潜在的神经保护作用。还评估了 1-11 的抗炎、抗病毒和细胞毒性活性。