Phomoidrides E-G, three dimeric anhydrides from the fungus Pleosporales sp. give new insight to the biosynthesis of phomoidrides

被引:5
|
作者
Zhang, Lihua [1 ,2 ]
Wang, Yanan [1 ]
Zhang, Le [1 ]
Liu, Bingyu [1 ]
Zhang, Chen [1 ]
Yan, Daojiang [1 ]
Bai, Jian [1 ]
Hu, Youcai [1 ]
机构
[1] Chinese Acad Med Sci & Peking Union Med Coll, Inst Mat Med, State Key Lab Bioact Substance & Funct Nat Med, Beijing 100050, Peoples R China
[2] Tianjin Univ Tradit Chinese Med, State Key Lab Component Based Chinese Med, Tianjin Key Lab TCM Chem & Anal, Inst Tradit Chinese Med, Tianjin 300193, Peoples R China
基金
中国国家自然科学基金;
关键词
RAS FARNESYLATION INHIBITORS; UNIDENTIFIED FUNGUS; CP-225,917; CP-263,114; PREDICTION;
D O I
10.1039/d1qo01119g
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Three phomoidride-type dimeric anhydrides, phomoidrides E-G (1-3), were isolated from the fungus Pleosporales sp. Their structures were elucidated by comprehensive spectroscopic analyses. Phomoidride E (1) possesses a totally new caged tricyclo[5.3.2.0(2;8)]dodecane carbon skeleton with a newly formed five-membered bridged ring through a C-C bond. Phomoidride F (2) features a unique caged ring system containing a bicyclo[4.3.1]deca-2,6-diene fused with an additional gamma-lactone ring. The identification of 1-3 offers new insight into phomoidride biosynthesis, where a new dimerization strategy with a key Claisen-like intermediate M1 instead of the previously proposed aldol-like product could be involved. 1 shows potent inhibitory activity against the HeLa cell line with an IC50 value of 1.41 mu M.
引用
收藏
页码:5926 / 5933
页数:9
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