Polycyclic Polyprenylated Acylphloroglucinol Congeners Possessing Diverse Structures from Hypericum henryi

被引:87
作者
Yang, Xing-Wei [1 ,4 ]
Li, Ming-Min [1 ]
Liu, Xia [1 ,4 ]
Ferreira, Daneel [2 ]
Ding, Yuanqing [3 ]
Zhang, Jing-Jing [1 ,4 ]
Liao, Yang [1 ,4 ]
Qin, Hong-Bo [1 ]
Xu, Gang [1 ]
机构
[1] Chinese Acad Sci, Kunming Inst Bot, State Key Lab Phytochem & Plant Resources West Ch, Kunming 650201, Peoples R China
[2] Univ Mississippi, Sch Pharm, Div Pharmacognosy, Dept Biomol Sci, University, MS 38677 USA
[3] Univ Mississippi, Sch Pharm, Natl Ctr Nat Prod Res, Res Inst Pharmaceut Sci, University, MS 38677 USA
[4] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
来源
JOURNAL OF NATURAL PRODUCTS | 2015年 / 78卷 / 04期
关键词
ST JOHNS WORT; PHLOROGLUCINOL DERIVATIVES; BENZOPHENONE DERIVATIVES; SUBSP URALOIDES; HYPERFORIN; PERFORATUM; SAMPSONII; GUTTIFERAE; BIOSYNTHESIS; ADHYPERFORIN;
D O I
10.1021/acs.jnatprod.5b00057
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Polycyclic polyprenylated acylphloroglucinols (PPAPs) are a class of hybrid natural products sharing the mevalonate/methylerythritol phosphate and polyketide biosynthetic pathways and showing considerable structural and bioactive diversity. In a systematic phytochemical investigation of Hypericum henryi, 40 PPAP-type derivatives, including the new compounds hyphenrones G-Q, were obtained. These compounds represent 12 different structural types, including four unusual skeletons exemplified by 5, 8, 10, and 17. The 12 different core structures found are explicable in terms of their biosynthetic origin. The structure of a known PPAP, perforatumone, was revised to hyphenrone A (5) by NMR spectroscopic and biomimetic synthesis methods. Several compounds exhibited inhibitory activities against acetylcholinesterase and human tumor cell lines. This study deals with the structural diversity, function, and biogenesis of natural PPAPs.
引用
收藏
页码:885 / 895
页数:11
相关论文
共 57 条
[1]   Biosynthesis of hyperforin in Hypericum perforatum [J].
Adam, P ;
Arigoni, D ;
Bacher, A ;
Eisenreich, W .
JOURNAL OF MEDICINAL CHEMISTRY, 2002, 45 (21) :4786-4793
[2]  
ALLEY MC, 1988, CANCER RES, V48, P589
[3]  
Avato P, 2005, STUD NAT PROD CHEM, V30, P603
[4]   Biotransformations of Prenylated Hop Flavonoids for Drug Discovery and Production [J].
Bartmanska, Agnieszka ;
Tronina, Tomasz ;
Poplonski, Jaroslaw ;
Huszcza, Ewa .
CURRENT DRUG METABOLISM, 2013, 14 (10) :1083-1097
[5]  
Biber N, 2011, NAT CHEM, V3, P938, DOI [10.1038/NCHEM.1170, 10.1038/nchem.1170]
[6]   Prenylated Isoflavonoids: Botanical Distribution, Structures, Biological Activities and Biotechnological Studies. An Update (1995-2006) [J].
Botta, Bruno ;
Menendez, Pilar ;
Zappia, Giovanni ;
de Lima, Roberto Alves ;
Torge, Roberta ;
Delle Monache, Giuliano .
CURRENT MEDICINAL CHEMISTRY, 2009, 16 (26) :3414-3468
[7]   The first prenylation step in hyperforin biosynthesis [J].
Boubakir, Z ;
Beuerle, T ;
Liu, B ;
Beerhues, L .
PHYTOCHEMISTRY, 2005, 66 (01) :51-57
[8]   Polycyclic Polyprenylated Acylphloroglucinols and Chromone O-Glucosides from Hypericum henryi subsp uraloides [J].
Chen, Xuan-Qin ;
Li, Yan ;
Cheng, Xiao ;
Wang, Kou ;
He, Juan ;
Pan, Zheng-Hong ;
Li, Ming-Ming ;
Peng, Li-Yan ;
Xu, Gang ;
Zhao, Qin-Shi .
CHEMISTRY & BIODIVERSITY, 2010, 7 (01) :196-204
[9]  
Cholpisut T., 2012, J NAT PRODUCTS, V75, P1660
[10]   Polycyclic polyprenylated acylphloroglucinols [J].
Ciochina, Roxana ;
Grossman, Robert B. .
CHEMICAL REVIEWS, 2006, 106 (09) :3963-3986