Diterpenoids and Triterpenoids from the Aerial Parts of Isodon serra and Their Biological Activities

被引:0
|
作者
Ren, Wen-Jing [1 ]
Jiang, Rong [1 ]
Ng, Kei-Fong [1 ]
Bao, Meng-Yu [1 ]
Liu, Xiao-Mei [1 ]
Zhang, Wei [1 ]
Jiang, Zhi-Hong [1 ]
Liu, Yu-Hong [2 ]
Zhu, Guo-Yuan [1 ]
机构
[1] Macau Univ Sci & Technol, Macau Inst Appl Res Med & Hlth, State Key Lab Qual Res Chinese Med, Guangdong Hong Kong Macao Joint Lab Resp Infect Di, Hong Kong 999078, Guangdong, Peoples R China
[2] Shandong Univ Tradit Chinese Med, Sch Pharmaceut Sci, Jinan 250355, Peoples R China
来源
ACS OMEGA | 2024年 / 9卷 / 49期
关键词
ENT-KAURANE DITERPENOIDS; RABDOSIA-SERRA; TORMENTIC ACID; MASLINIC ACID; IDENTIFICATION; PRINCIPLES; LEAVES;
D O I
10.1021/acsomega.4c08821
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Five undescribed diterpenoids, serranins A-E (1-5), and four novel triterpenoids, serratic acids A-D (6-9), along with 32 known terpenoids (10-41) were isolated from the aerial parts of Isodon serra. The planar structures of 1-9 and their relative configurations were established on the basis of extensive spectroscopic analysis. Structurally, compounds 6-9 are the first examples of 18,19-seco-ursane p-coumaric or ferulic esters, while compounds 1-5 further enriched the plant's diterpene profile. Bioactivity evaluation revealed that four diterpenoids (2, 10, 12, and 13) exhibited potent cytotoxic activity against four cancer cell lines (B16-F10, A375, A549, and MDA-MB-231) with IC50 values below 10 mu M. Remarkably, 7 and 38 exhibited a comparable antimelanogenesis effect to that of positive control (kojic acid) in B16-F10 cells.
引用
收藏
页码:48791 / 48801
页数:11
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