Mei Yu-Dan, Li Hai-Bo, Pang Qian-Qian, Li Ting, Pan Da-Bo, Dai Yi, Qin Da-Peng, Meng He, Yao Xin-Sheng, Yu Yang
Institute of Traditional Chinese Medicine & Natural Products, College of Pharmacy, Jinan University Guangzhou 510632 P. R. China
Xiangxue Academician Workstation, Xiangxue Pharmaceutical Co. Ltd. Guangzhou 510663 P. R. China.
RSC Adv. 2019 Jul 16;9(38):22011-22016. doi: 10.1039/c9ra04029c. eCollection 2019 Jul 11.
Lonimacranaldes A and B (1 and 2), along with one biogenetically related intermediate, lonimacranalde C (3), were isolated from the flower buds of . Characterized by an iridoid structure and an additional C-6 unit with an aldehyde group, compounds 1 and 2 are the first examples of hybrid iridoids possessing an unexpected 6/5/6 fused tricyclic ring system, while compound 3 serves as an important precursor for their generation. The structures of lonimacranaldes A-C (1-3) were revealed by extensive spectroscopic and X-ray diffraction analyses. A plausible biogenetic pathway for them was proposed. Compound 3 showed anti-inflammatory activities by inhibiting the production of IL-6 on LPS-induced RAW 264.7 cells with an IC value of 6.33 μM.
从[植物名称]的花芽中分离出了洛尼马克兰醛A和B(1和2),以及一种生源相关中间体洛尼马克兰醛C(3)。化合物1和2具有环烯醚萜结构以及一个带有醛基的额外C-6单元,是具有意外的6/5/6稠合三环体系的杂交环烯醚萜的首个实例,而化合物3是它们生成的重要前体。通过广泛的光谱分析和X射线衍射分析揭示了洛尼马克兰醛A - C(1 - 3)的结构。并提出了一个合理的生源途径。化合物3通过抑制脂多糖诱导的RAW 264.7细胞中IL-6的产生而显示出抗炎活性,IC值为6.33 μM。