Bicyclic polyprenylated acylphloroglucinol-related meroterpenoids as potent DRAK2 inhibitors from Hypericum patulum

被引:1
|
作者
Huang, Jin-Chang [1 ]
Jia, Xin-Yu [2 ]
Lv, Yi-Fan [1 ]
Xu, Hong-Hong [3 ]
Han, Ming [3 ]
Yu, Qiang-Qiang [1 ]
Lu, Yu-Ting [3 ]
Yang, Hong-Xun [4 ]
Yang, Yang [3 ,5 ,6 ]
Li, Jing-Ya [3 ,5 ,6 ]
Hou, Ai-Jun [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Frontiers Sci Ctr Drug Target Identificat, Sch Pharmaceut Sci, Shanghai 200240, Peoples R China
[2] Fudan Univ, Sch Pharm, Shanghai 201203, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Mat Med, Natl Ctr Drug Screening, State Key Lab Drug Res, Shanghai 201203, Peoples R China
[4] Sinopharm Chem Reagent Co Ltd, Shanghai 200002, Peoples R China
[5] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[6] Univ Chinese Acad Sci, Hangzhou Inst Adv Study, Sch Pharmaceut Sci & Technol, Hangzhou 310024, Peoples R China
基金
中国国家自然科学基金;
关键词
Hypericum patulum; Hypericaceae; Meroterpenoids; Hyperpatins A-H; Death-associated protein kinase-related; apoptosis-inducing kinase 2; Glucose-stimulated insulin secretion; ABSOLUTE-CONFIGURATION; DERIVATIVES; HYPERFORIN; DISCOVERY; APOPTOSIS; 1,2-DIOLS; ANALOGS;
D O I
10.1016/j.phytochem.2024.114375
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
As a both edible and medicinal plant, Hypericum patulum (Hypericaceae) is used as a natural herbal tea, scented tea, and folk medicine. In this study, eight undescribed bicyclic polyprenylated acylphloroglucinol-related meroterpenoids named hyperpatins A-H, along with eight known ones, were isolated from this plant. Their structures were elucidated on the basis of spectroscopic techniques, chemical method, X-ray crystallographic experiments, and electronic circular dichroism analyses. Hyperpatins A-H possess a characteristic pyran ring system diversely fused with the bicyclo[3.3.1]nonane-2,4,9-trione core, and hyperpatins C and D incorporate a unique alpha,beta-unsaturated aldehyde moiety. Some of the isolates exhibited potent inhibitory effects on death-associated protein kinase-related apoptosis-inducing kinase 2 with IC50 values ranging from 2.60 +/- 0.29 to 17.93 +/- 3.08 mu M. This is the first report of DRAK2 inhibitory activity for acylphloroglucinol-related meroterpenoids. The most active molecule hyperpatins C showed binding affinity with DRAK2 by hydrogen-bond and hydrophobic interactions in molecular docking and promoted the glucose-stimulated insulin secretion ability of primary islets.
引用
收藏
页数:10
相关论文
共 13 条
  • [11] Discovery of benzofuran-3(2H)-one derivatives as novel DRAK2 inhibitors that protect islet β-cells from apoptosis
    Wang, Sheng
    Xu, Lei
    Lu, Yu-Ting
    Liu, Yu-Fei
    Han, Bing
    Liu, Ting
    Tang, Jie
    Li, Jia
    Wu, Jiangping
    Li, Jing-Ya
    Yu, Li-Fang
    Yang, Fan
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2017, 130 : 195 - 208
  • [12] Norwilsonnol A, an immunosuppressive polycyclic polyprenylated acylphloroglucinol with a spiro[5-oxatricyclo[6.4.0.03,7]dodecane-6′,1-1′,2′-dioxane] system from Hypericum wilsonii
    Xie, Shuangshuang
    Zhou, Yuan
    Tan, Xiaosheng
    Sun, Weiguang
    Duan, Yulin
    Feng, Hao
    Sun, Lingjuan
    Guo, Yi
    Shi, Zhengyi
    Hao, Xincai
    Chen, Gang
    Qi, Changxing
    Zhang, Yonghui
    ORGANIC CHEMISTRY FRONTIERS, 2021, 8 (10): : 2280 - 2286
  • [13] Caged polycyclic polyprenylated acylphloroglucinols as Cav3.2 low voltage-gated Ca2+ channel inhibitors from Hypericum curvisepalum
    Ye, Yan-Song
    Liu, Rui
    Jiang, Na-Na
    Li, Song-Yu
    Nian, Yin
    Xu, Gang
    CHEMICAL COMMUNICATIONS, 2022, 58 (94) : 13135 - 13138