Main observation and conclusion Four new N-methoxyindolediketopiperazines(acrozines D—G,1—4)and six known congeners(5—10)were purified from the organic extract of Acrostalagmus luteoalbus TK-43,which was a marine a...Main observation and conclusion Four new N-methoxyindolediketopiperazines(acrozines D—G,1—4)and six known congeners(5—10)were purified from the organic extract of Acrostalagmus luteoalbus TK-43,which was a marine algal-derived fungus obtained from Codium fragile.Their structures were determined by interpretation of NMR and mass spectroscopic data.The structures of compounds 1,2,and 4 including their absolute configurations were confirmed by single-crystal X-ray diffraction,while the absolute configuration of compound 3 was elucidated by comparative analysis of ECD and TDDFT-ECD calculations.Compounds 1—4,with a unique methoxy substitution at N-2,were rarely discovered among indolediketopiperazine alkaloids.All these compounds were evaluated for antimicrobial activities against human-and aquatic-pathogenic bacteria and plant-related pathogenic fungi,with compounds 5 and 7 exhibiting potent activity against Edwardsiella icataluri(MIC=3 and 5μmol/L,respectively),while compound 9 displayed a broad spectrum of antibacterial activities.The four new compounds were further tested for anti-acetylcholinesterase(AChE)properties,and compound 3 exhibited inhibitory activity with IC_(50)value of 8.4μmol/L.展开更多
基金supported by the National Natural Science Foundation of China(81673351)by the European Commission under the program"Marie Curie Actions-Interna-tional Research Staff Exchange Scheme"(IRSES,Grant Agreement Number:PIRSES-GA-2011-295226)B.-G.W.appreciates the support of Taishan Scholar Project from Shandong Province of China(ts201511060).
文摘Main observation and conclusion Four new N-methoxyindolediketopiperazines(acrozines D—G,1—4)and six known congeners(5—10)were purified from the organic extract of Acrostalagmus luteoalbus TK-43,which was a marine algal-derived fungus obtained from Codium fragile.Their structures were determined by interpretation of NMR and mass spectroscopic data.The structures of compounds 1,2,and 4 including their absolute configurations were confirmed by single-crystal X-ray diffraction,while the absolute configuration of compound 3 was elucidated by comparative analysis of ECD and TDDFT-ECD calculations.Compounds 1—4,with a unique methoxy substitution at N-2,were rarely discovered among indolediketopiperazine alkaloids.All these compounds were evaluated for antimicrobial activities against human-and aquatic-pathogenic bacteria and plant-related pathogenic fungi,with compounds 5 and 7 exhibiting potent activity against Edwardsiella icataluri(MIC=3 and 5μmol/L,respectively),while compound 9 displayed a broad spectrum of antibacterial activities.The four new compounds were further tested for anti-acetylcholinesterase(AChE)properties,and compound 3 exhibited inhibitory activity with IC_(50)value of 8.4μmol/L.
