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Sesquiterpene and Sorbicillinoid Glycosides from the Endophytic Fungus Trichoderma longibrachiatum EN-586 Derived from the Marine Red Alga Laurencia obtusa
被引:14
|作者:
Wang, Ying
[1
,2
,3
]
Li, Xiao-Ming
[1
,2
,4
]
Yang, Sui-Qun
[1
,2
,4
]
Zhang, Fan-Zhong
[1
,2
,3
]
Wang, Bin-Gui
[1
,2
,3
,4
]
Li, Hong-Lei
[1
,2
,4
]
Meng, Ling-Hong
[1
,2
,3
,4
]
机构:
[1] Chinese Acad Sci, Inst Oceanol, CAS & Shandong Prov Key Lab Expt Marine Biol, Nanhai Rd 7, Qingdao 266071, Peoples R China
[2] Qingdao Natl Lab Marine Sci & Technol, Lab Marine Biol & Biotechnol, Wenhai Rd 1, Qingdao 266237, Peoples R China
[3] Univ Chinese Acad Sci, Yuquan Rd 19A, Beijing 100049, Peoples R China
[4] Chinese Acad Sci, Ctr Ocean Megasci, Nanhai Rd 7, Qingdao 266071, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Trichoderma longibrachiatum;
sesquiterpene glycoside;
secondary metabolites;
antimicrobial activity;
D O I:
10.3390/md20030177
中图分类号:
R914 [药物化学];
学科分类号:
100701 ;
摘要:
An unusual sesquiterpene glycoside trichoacorside A (1) and two novel sorbicillinoid glycosides sorbicillisides A (2) and B (3), together with a known compound sorbicillin (4), were isolated and identified from the culture extract of an endophytic fungus Trichoderma longibrachiatum EN-586, obtained from the marine red alga Laurencia obtusa. Trichoacorside A (1) is the first representative of a glucosamine-coupled acorane-type sesquiterpenoid. Their structures were elucidated based on detailed interpretation of NMR and mass spectroscopic data. The absolute configurations were determined by X-ray crystallographic analysis, chemical derivatization, and DP4+ probability analysis. The antimicrobial activities of compounds 1-4 against several human, aquatic, and plant pathogens were evaluated.
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页数:11
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