Phomopsols A and B from the Mangrove Endophytic Fungus Phomopsis sp. xy21: Structures, Neuroprotective Effects, and Biogenetic Relationships

被引:29
|
作者
Li, Wan-Shan [1 ]
Hu, Han-Bo [2 ]
Huang, Zhong-Hui [1 ]
Yan, Ren-Jie [1 ]
Tian, Li-Wen [1 ]
Wu, Jun [1 ]
机构
[1] Southern Med Univ, Sch Pharmaceut Sci, 1838 Guangzhou Ave North, Guangzhou 510515, Guangdong, Peoples R China
[2] Jinan Univ, Coll Pharm, Marine Drugs Res Ctr, 601 Huangpu Ave West, Guangzhou 510632, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
ALKALOIDS; RHAZINILAM;
D O I
10.1021/acs.orglett.9b02906
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A polyketide-derived alkaloid featuring a unique 3,4-dihydro-2H-indeno[1,2-b]pyridine 1-oxide motif, named phomopsol A (1), and a highly oxidized polyketide containing a new 3,5-dihydro-2H-2,5-methanobenzo [e][1,4]-dioxepine moiety, named phomopsol B (2), were isolated from the Thai mangrove endophytic fungus Phomopsis sp. xy21, together with the related biosynthetic polyketide 3. The structures of 1-3 were unambiguously established by single-crystal X-ray diffraction analysis (Cu K alpha), and their neuroprotective effects in PC12 cells were evaluated. The biosynthetic origins of 1-3 are proposed.
引用
收藏
页码:7919 / 7922
页数:4
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