Glucoconjugated Monoterpene Indole Alkaloids from Uncaria rhynchophylla

• Published in: Journal of natural products (Washington, D.C.) D.C.), 2019-12, Vol.82 (12), p.3288-3301
• Main Authors: Guo, Qiang, Si, Xiali, Shi, Yuntao, Yang, Hongshuai, Liu, Xinyu, Liang, Hong, Tu, Pengfei, Zhang, Qingying
• Format: Article
• Language: English
• ISSN: 0163-3864; 1520-6025
• DOI: 10.1021/acs.jnatprod.9b00490

Twenty-six glucoconjugated monoterpene indole alkaloids, including 12 new compounds, rhynchophyllosides A–L (1–12), and 14 known ones, 13–26, were obtained from the hook-bearing stems of Uncaria rhynchophylla (Miq.) Miq. ex Havil. Their structures were unambiguously elucidated by analyses of UV, MS, NMR, ECD, and single-crystal X-ray diffraction data. The ESI-MS n behavior of the new glucoalkaloids was also elucidated. Although comprising the same glucosyl moiety, the aglycone skeletons and glucosidic numbers and linkage varied greatly, implying the diversity in biosynthetic pathways. This is the first report of such structurally diverse glucoconjugated monoterpene indole alkaloids from U. rhynchophylla. Compound 1 represents a new subtype of oxindole alkaloid with a seven-membered D-ring, 10 is a rare monoterpene indole alkaloid with the glucosyl moiety located at C-9, 4 and 5 are the first two oxindole alkaloid diglycosides, and 11 and 12 represent the first two examples of alkaloids with a quinolone nucleus from the genus Uncaria. Compound 10 exhibited moderate acetylcholinesterase (AChE) inhibitory activity with an IC50 value of 10.5 μM. Molecular docking was performed to explore the binding mode of inhibitor 10 at the active site of AChE.