Chemical Diversity from a Chinese Marine Red Alga, Symphyocladia latiuscula

被引:13
作者
Xu, Xiuli [1 ]
Yang, Haijin [1 ,2 ]
Khalil, Zeinab G. [3 ]
Yin, Liyuan [1 ]
Xiao, Xue [3 ]
Neupane, Pratik [3 ]
Bernhardt, Paul V. [4 ]
Salim, Angela A. [3 ]
Song, Fuhang [2 ]
Capon, Robert J. [3 ]
机构
[1] China Univ Geosci, Sch Ocean Sci, Beijing 100083, Peoples R China
[2] Chinese Acad Sci, Inst Microbiol, CAS Key Lab Pathogen Microbiol & Immunol, Beijing 100101, Peoples R China
[3] Univ Queensland, Inst Mol Biosci, Brisbane, Qld 4072, Australia
[4] Univ Queensland, Sch Chem & Mol Biosci, Brisbane, Qld 4072, Australia
关键词
marine red alga; Symphyocladia latiuscula; bromophenols; symphyocladins; aconitates; RHODOMELA-CONFERVOIDES; 4; BROMOPHENOLS;
D O I
10.3390/md15120374
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
This study describes an investigation into secondary metabolites that are produced by a marine red alga, Symphyocladia latiuscula, which was collected from coastal waters off Qingdao, China. A combination of normal, reversed phase, and gel chromatography was used to isolate six citric acid derived natural products, aconitates A-F (1-6), together with two known and ten new polybrominated phenols, symphyocladins C/D (7a/b), and symphyocladins H-Q (8a/b, 9a/b and 10-15), respectively. Structure elucidation was achieved by detailed spectroscopic (including X-ray crystallographic) analysis. We propose a plausible and convergent biosynthetic pathway involving a key quinone methide intermediate, linking aconitates and symphyocladins.
引用
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页数:10
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