Discovery of Ingenane Diterpenoids from Euphorbia hylonoma as Antiadipogenic Agents

被引:0
|
作者
Wu, Shu-Qi [1 ]
Zhu, Xinying [1 ]
Yuan, Tao [2 ]
Yuan, Fang-Yu [1 ]
Zhou, Shiyou [3 ]
Huang, Dong [1 ]
Wang, Ying [4 ]
Tang, Gui-Hua [1 ]
Huang, Zhi-Shu [1 ]
Chen, Xin [5 ]
Yin, Sheng [1 ]
机构
[1] Sun Yat Sen Univ, Sch Pharmaceut Sci, Southern Marine Sci & Engn Guangdong Lab Zhuhai, Guangzhou 510006, Peoples R China
[2] Jiangxi Normal Univ, Sch Hlth, Nanchang 330022, Peoples R China
[3] Guangdong Vis & Eye Inst, Guangzhou 510060, Peoples R China
[4] Jinan Univ, Int Cooperat Lab Tradit Chinese Med Modernizat & I, Minist Educ MOE China, Guangzhou 510632, Peoples R China
[5] Wuhan Polytech Univ, Sch Life Sci & Technol, Wuhan 430023, Peoples R China
来源
JOURNAL OF NATURAL PRODUCTS | 2023年 / 86卷 / 12期
基金
中国国家自然科学基金;
关键词
BIOLOGICAL EVALUATION; OBESITY; ADIPOGENESIS/LIPOGENESIS; DERIVATIVES; INHIBITORS; KANSUI;
D O I
10.1021/acs.jnatprod.3c00822
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Thirteen new Euphorbia diterpenoids, euphylonanes A-M (1-13), and eight known ones were isolated from the whole plants of Euphorbia hylonoma. Compounds 1 and 2 are two rearranged ingenanes bearing a rare 6/6/7/3-fused ring system. Compound 3 represents the first example of a 9,10-epoxy tigliane, while 4-21 are typical ingenanes varying with substituents. Structures were elucidated using a combination of spectroscopic, computational, and chemical methods. Most ingenanes exerted a significant antiadipogenic effect in 3T3-L1 adipocytes, among which 4 was the most active with an EC50 value of 0.60 +/- 0.27 mu M. Mechanistic study revealed that 4 inhibited the adipogenesis and lipogenesis in adipocytes via activation of the AMPK signaling pathway.
引用
收藏
页码:2691 / 2702
页数:12
相关论文
共 50 条
  • [1] Ingenane diterpenoids from Euphorbia esula
    Lu, Zhi-Qiang
    Yang, Min
    Zhang, Jin-Qiang
    Chen, Guang-Tong
    Huang, Hui-Lian
    Guan, Shu-Hong
    Ma, Chao
    Liu, Xuan
    Guo, De-An
    PHYTOCHEMISTRY, 2008, 69 (03) : 812 - 819
  • [2] New ingenane and ingol diterpenoids from Euphorbia royleana
    Wu, Shuqi
    Gan, Lu
    Su, Tong
    Wei, Xun
    Yin, Sheng
    NATURAL PRODUCT RESEARCH, 2023, 37 (07) : 1130 - 1137
  • [3] LATHYRANE AND INGENANE DITERPENOIDS FROM EUPHORBIA-MICRACTINA
    SHI, JG
    JIA, ZJ
    YANG, L
    PLANTA MEDICA, 1994, 60 (06) : 588 - 589
  • [4] Discovery of ingenane and jatrophane diterpenoids from Euphorbia esula as inhibitors of RANKL-induced osteoclastogenesis
    Yuan, Shengheng
    Zhang, Yuting
    Hua, Pei
    Zhou, Huihao
    Xu, Jun
    Gu, Qiong
    FITOTERAPIA, 2020, 146
  • [5] Phytotoxic ent-Isopimarane-Type Diterpenoids from Euphorbia hylonoma
    Wei, Wen-Jun
    Song, Qu-Yan
    Zheng, Zai-Qin
    Yao, Xiaojun
    Li, Ya
    Gao, Kun
    JOURNAL OF NATURAL PRODUCTS, 2018, 81 (11): : 2381 - 2391
  • [6] Ingenane and jatrophane diterpenoids from Euphorbia kansui and their antiproliferative effects
    Meng, Xian-Hua
    Wang, Kai
    Chai, Tian
    Guo, Zhi-Ying
    Zhao, Ming
    Yang, Jun-Li
    PHYTOCHEMISTRY, 2020, 172
  • [7] Anti-inflammatory Ingenane Diterpenoids from the Roots of Euphorbia kansui
    Zhang, Jun-Sheng
    Weng, Han-Zhuang
    Huang, Jia-Luo
    Tang, Gui-Hua
    Yin, Sheng
    PLANTA MEDICA, 2018, 84 (18) : 1334 - 1339
  • [8] Ingenane diterpenoids with anti-inflammatory activity from Euphorbia antiquorum
    Ma, Ren-Fen
    Wu, Qian
    Pan, Yin-Po
    Liu, Hu
    Zhuang, Xin-Cheng
    Zhang, Hua
    FITOTERAPIA, 2025, 180
  • [9] Potent Anti-HIV Ingenane Diterpenoids from Euphorbia ebracteolata
    Huang, Ya-Si
    Lu, Yan
    Chen, Chin-Ho
    Lee, Kuo-Hsiung
    Chen, Dao-Feng
    JOURNAL OF NATURAL PRODUCTS, 2019, 82 (06): : 1587 - 1592
  • [10] Jatrophane and ingenane diterpenoids with anti-inflammatory activity from Euphorbia esula
    Li, Yu-Peng
    Li, Ying
    Gao, Wen-Jing
    Fang, Chu-Hong
    Lv, Ming-Jun
    Yue, Jian-Min
    Yu, Jin-Hai
    PHYTOCHEMISTRY, 2025, 232