Aspersymmetide A, a New Centrosymmetric Cyclohexapeptide from the Marine-Derived Fungus Aspergillus versicolor

被引:25
作者
Hou, Xue-Mei [1 ,2 ,3 ]
Zhang, Ya-Hui [1 ,2 ]
Hai, Yang [1 ,2 ]
Zheng, Ji-Yong [3 ]
Gu, Yu-Cheng [4 ]
Wang, Chang-Yun [1 ,2 ,5 ]
Shao, Chang-Lun [1 ,2 ,3 ]
机构
[1] Ocean Univ China, Sch Med & Pharm, Key Lab Marine Drugs, Minist Educ China, Qingdao 266003, Peoples R China
[2] Qingdao Natl Lab Marine Sci & Technol, Lab Marine Drugs & Bioprod, Qingdao 266200, Peoples R China
[3] Luoyang Ship Mat Res LSMRI, State Key Lab Marine Corros & Protect, Qingdao 266061, Peoples R China
[4] Jealotts Hill Int Res Ctr, Syngenta, Bracknell RG42 6EY, Berks, England
[5] Ocean Univ China, Inst Evolut & Marine Biodivers, Qingdao 266003, Peoples R China
基金
中国国家自然科学基金;
关键词
gorgonian-derived fungus; Carijoa sp; Aspergillus versicolor; centrosymmetric cyclohexapeptide; cytotoxicity; BIOLOGICAL-ACTIVITIES; FUSARIUM-OXYSPORUM; NATURAL-PRODUCTS; CELL; CYCLODEPSIPEPTIDE; BASSIANOLIDE; DERIVATIVES; ENNIATINS; POTENT; CONSTITUENTS;
D O I
10.3390/md15110363
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A new centrosymmetric cyclohexapeptide, aspersymmetide A (1), together with a known peptide, asperphenamate (2), was isolated from the fungus Aspergillus versicolor isolated from a gorgonian coral Carijoa sp., collected from the South China Sea. The chemical structure of 1 was elucidated by analyzing its NMR spectroscopy and MS spectrometry data, and the absolute configurations of the amino acids of 1 were determined by Marfey's method and UPLC-MS analysis of the hydrolysate. Aspersymmetide A (1) represents the first example of marine-derived centrosymmetric cyclohexapeptide. Moreover, 1 exhibited weak cytotoxicity against NCI-H292 and A431 cell lines at the concentration of 10 M.
引用
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页数:8
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