Structural and spectral assignments of six anthraquinone derivatives from the mangrove fungus (ZSUH-36)

被引:30
作者
Shao, Changlun [1 ,2 ]
Wang, Changyun [2 ]
Wei, Meiyan [2 ,3 ]
Li, Shangde [3 ]
She, Zhigang [1 ]
Gu, Yucheng [4 ]
Lin, Yongcheng [1 ]
机构
[1] Sun Yat Sen Zhongshan Univ, Sch Chem & Chem Engn, Guangzhou 510275, Guangdong, Peoples R China
[2] Ocean Univ China, Sch Med & Pharm, Qingdao 266003, Peoples R China
[3] Guang Dong Med Coll, Sch Pharm, Dongguan 523808, Peoples R China
[4] Syngenta Jealotts Hill Int Res Ctr, Bracknell RG42 6EY, Berks, England
基金
中国国家自然科学基金;
关键词
NMR; H-1; C-13; 2D NMR; anthraquinone; secondary metabolites; structure elucidation;
D O I
10.1002/mrc.2266
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A new natural product named 6,8,1'-tri-O-methyl averantin has been isolated together with five known anthraquinones 1'-O-methyl averantin(2), 6,8-di-O-methyl averufin (3) averufin (4), versicolorin C (5) and 6,8-di-O-methyl averufanin (6) from a mangrove endophytic fungus ZSUH-36 collected from the South China Sea. NMR techniques including COSY, HMQC, and HMBC were used to elucidate the structures of these compounds. We report the unambiguous assignments of the H-1 and C-13 NMR spectra of the new compound 6,8,1'-tri-O-methyl averantin(l). Copyright (c) 2008 John Wiley & Sons, Ltd.
引用
收藏
页码:886 / 889
页数:4
相关论文
共 11 条
[11]  
Zhu F, 2004, CHINESE J ORG CHEM, V24, P1114