Yuexiandajisu diterpenoids from Euphorbia ebracteolata Hayata (Langdu roots): An overview

被引:5
作者
Bailly, Christian [1 ,2 ,3 ]
机构
[1] OncoWitan, Consulting Sci Off, F-59290 Lille, France
[2] Univ Lille, Inst Chim Pharmaceut Albert Lespagnol ICPAL, Fac Pharm, 3 rue Prof Laguesse, F-59000 Lille, France
[3] Univ Lille, CNRS, Inserm, CHU Lille,UMR9020, F-59000 Lille, France
关键词
Cancer; Diterpenoid; Euphorbia ebracteolata; Langdu TCM; Yuexiandajisu; CASBANE DITERPENOIDS; CYTOTOXIC DITERPENOIDS; STELLERA-CHAMAEJASME; CONSTITUENTS; GROWTH;
D O I
10.1016/j.phytochem.2023.113784
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
The roots of the plant Euphorbia ebracteolata Hayata (Yue Xian Da Ji) are commonly used in traditional Chinese medicine to treat multiple diseases such as chronic liver diseases, oedema, pulmonary diseases and cancer. It is the main ingredient of the TCM called Langdu which can be prepared also from roots of E. fischeriana Steud. and occasionally from Stellera chamaejasme species. Numerous bioactive natural products have been isolated from E. ebracteolata including a large diversity of diterpenoids with anti-inflammatory and anticancer properties. One little series of compounds has been named yuexiandajisu (A, B, C, D, D1, E, F) which comprises two casbane-, one isopimarane-, two abietane-, and two rosane-type diterpenes including a dimeric molecule. The origin, structural diversity and properties of these little-known natural products is discussed here. Several of these compounds have been identified in the roots of other Euphorbia species, notably the potent phytotoxic agent yuexiandajisu C. The abietane diterpenes yuexiandajisu D-E exhibit marked anticancer properties but their mechanism of action remains unresolved. The dimeric compound, renamed yuexiandajisu D1, also exhibit anti-proliferative properties against cancer cell lines, unlike the rosane diterpene yuexiandajisu F. The structural or functional analogy with other diterpenoids is discussed.
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页数:9
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共 80 条
[31]   Pharmacokinetics and tissue distribution of Ebracteolatain A, a potential anti-cancer compound, as determined by an optimized ultra-performance liquid chromatography tandem mass spectrometry method [J].
Lv, Lei ;
Liu, Yue ;
Li, Ling ;
Qin, Fu-Li ;
Li, Cheng-Jian ;
Zhou, Yan-Qing ;
Zhou, Yan-Ni ;
Wang, Hui ;
Jiao, Yang ;
Zhao, Liang .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2019, 169 :279-287
[32]   Abietane Diterpernoids from the Roots of Euphorbia ebracteolata [J].
Ma Y.-L. ;
Tang X.-H. ;
Yuan W.-J. ;
Ding X. ;
Di Y.-T. ;
Hao X.-J. .
Natural Products and Bioprospecting, 2018, 8 (2) :131-135
[33]   Two New Rosane-Type Diterpenoids from Euphorbia ebracteolata HAYATA [J].
Mu, Shu-Zhen ;
Jiang, Chun-Rong ;
Huang, Tao ;
Hao, Xiao-Jiang .
HELVETICA CHIMICA ACTA, 2013, 96 (12) :2299-2303
[34]   Chukranoids A-I, isopimarane diterpenoids from Chukrasia velutina [J].
Nugroho, Alfarius Eko ;
Tange, Masaki ;
Kusakabe, Sumi ;
Hirasawa, Yusuke ;
Shirota, Osamu ;
Matsuno, Michiyo ;
Mizukami, Hajime ;
Tougan, Takahiro ;
Horii, Toshihiro ;
Morita, Hiroshi .
JOURNAL OF NATURAL MEDICINES, 2022, 76 (04) :756-764
[35]   Isolation, Structural Analysis and Biological Activity Assays of Biselisabethoxanes A and B: Two Dissymmetric Bis-Diterpenes from the Southwestern Caribbean Sea Gorgonian Coral Pseudopterogorgia elisabethae [J].
Rodriguez, Ileana I. ;
Rodriguez, Abimael D. ;
Barnes, Charles L. .
MOLECULES, 2022, 27 (22)
[36]   Two new casbane diterpenoids from the roots of Euphorbia pekinensis [J].
Shao, Feng-Guang ;
Bu, Ren ;
Zhang, Cui ;
Chen, Chao-Jun ;
Huang, Jian ;
Wang, Jin-Hui .
JOURNAL OF ASIAN NATURAL PRODUCTS RESEARCH, 2011, 13 (09) :805-810
[37]   Cytotoxic diterpenoids from the roots of Euphorbia ebracteolata [J].
Shi, HM ;
Williams, ID ;
Sung, HHY ;
Zhu, HX ;
Ip, NY ;
Min, ZD .
PLANTA MEDICA, 2005, 71 (04) :349-354
[38]   Cytotoxicity and molecular-docking approach of a new rosane-type diterpenoid from the roots of Euphorbia nematocypha [J].
Song, Nali ;
Zheng, Xi ;
Wang, Jiapeng ;
Zhu, Li ;
Wang, Chengyao ;
Cai, Le ;
Ding, Zhongtao .
FRONTIERS IN CHEMISTRY, 2022, 10
[39]   Chemical constituents from Stellera chamaejasme L. and chemotaxonomic significance [J].
Song, Qi ;
Li, Shi-Fang ;
Cheng, Zhuo-Yang ;
Song, Shao-Jiang ;
Huang, Xiao-Xiao .
BIOCHEMICAL SYSTEMATICS AND ECOLOGY, 2023, 107
[40]   Identification and characterisation of the Chinese herb Langdu by LC-MS/MS analysis [J].
Su, XL ;
Lin, RC ;
Wong, SK ;
Tsui, SK ;
Kwan, SY .
PHYTOCHEMICAL ANALYSIS, 2003, 14 (01) :40-47