Structurally diverse lanostane triterpenoids from medicinal and edible mushroom Ganoderma resinaceum Boud

被引:17
作者
Shi, Qiang-Qiang [1 ,2 ,3 ]
Huang, Yan-Jie [1 ,2 ,3 ]
Su, Hai-Guo [1 ,2 ,3 ]
Gao, Ya [1 ,2 ,3 ]
Lu, Shuang-Yang [1 ,2 ,3 ]
Peng, Xing-Rong [1 ,3 ]
Li, Xiao-Nian [1 ,3 ]
Zhou, Lin [1 ,3 ]
Qiu, Ming-Hua [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Kunming Inst Bot, State Key Lab Phytochem & Plant Resources West Ch, Kunming 650201, Yunnan, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Chinese Acad Sci, Yunnan Key Lab Nat Med Chem, Kunming 650201, Yunnan, Peoples R China
基金
中国国家自然科学基金;
关键词
FRUITING BODIES; INHIBITORY-ACTIVITY; LUCIDUM; ACIDS; METABOLITES; CYTOTOXICITY;
D O I
10.1016/j.bioorg.2020.103871
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
Ganoderma resinaceum is a multi-purpose herbal medicine that is homologous to functional food that has long been used for enhancing health and treating chronic hepatopathy in Traditional Chinese Medicine. In a search program to discover the key bioactive composition of G. resinaceum, sixteen new lanostane-type triterpenoids (1–16), and twenty known analogues (17–36) were isolated from the fruiting bodies of G. resinaceum. Spectroscopic analyses and X-ray crystallography were used to determine the new structures. Furthermore, the spectroscopic properties of 15β-hydroxy-4,4,14α- trimethyl-3,7,11,20-tetraoxo-5α-pregn-8-ene (15) and 15α-hydroxy-4,4,14α-trimethyl- 3,7,11,20-tetraoxo-5α-pregn-8-ene (34) indicated a potential structural misassignment of their analogues, lucidone E and lucidone H, reported previously. To probe this hypothesis, ROESY experiments and single-crystal X-ray diffraction analysis were conducted. These results undoubtedly reassigned the structure of lucidone E and lucidone H. Biological evaluation of the selected compounds disclosed that compounds 3, 4, 7/21, 11, 12, 13/14, 17, 18, 24/25, 27, 30, 31, and 35 had significant hepatoprotective activities, due to their remarkable in vitro inhibitory activities against the increase of ALT and AST levels in HepG2 cells induced by H2O2. © 2020 Elsevier Inc.
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页数:11
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