期刊文献+

海洋微生物次级代谢产物中醌类化合物的研究进展 被引量:5

Progress on Quinone Secondary Metabolites of Marine Microorganisms
原文传递
导出
摘要 对海洋微生物次级代谢产物的深入研究是开发新特效药物的一个十分重要的内容。分别介绍了近年来海洋微生物次级代谢产物中苯醌类、萘醌类和蒽醌类化合物的重要成果及最新进展,并对其发展趋势进行了展望。 Researching on the secondary metabolites of marine microorganisms is an important content in developing new specific pharmaceuticals. This paper described the recent study on benzoquinone, naphthoquinone, and anthraquinone metabolites of marine microorganisms, respectively. Their future developments were also discussed.
出处 《中国天然药物》 SCIE CAS CSCD 北大核心 2009年第1期71-80,共10页
基金 国家"863"计划(No2003AA624010 2006AA092422) 国家自然科学基金(No29672053 20072058 20572136) 广东省自然科学基金(No950026 980317) 南华大学博士启动基金(No5-2007-XQD-002)资助项目~~
关键词 海洋微生物 苯醌 萘醌 蒽醌 次级代谢产物 Marine microorganisms Benzoquinone Naphthoquinone Anthraquinone Secondary metabolites
  • 相关文献

参考文献16

  • 1朱峰,林永成,周世宁.南海海洋真菌#2526中蒽醌类代谢产物的研究[J].有机化学,2004,24(9):1114-1117. 被引量:12
  • 2林永成,周世宁,乐长高.海洋微生物活性代谢产物化学[J].大学化学,1996,11(6):1-7. 被引量:21
  • 3Hongxia Cui,K. A. Shaaban,S. Qin.Two Anthraquinone Compounds from a Marine Actinomycete Isolate M097 Isolated from Jiaozhou Bay[J].World Journal of Microbiology and Biotechnology.2006(12)
  • 4T. A. Kuznetsova,A. S. Dmitrenok,M. P. Sobolevskaya,L. S. Shevchenko,V. V. Mikhailov.Ubiquinone Q9 from a marine isolate of an actinobacterium Nocardia sp.[J].Russian Chemical Bulletin.2002(10)
  • 5Y. Yamaguchi,R. Masuma,R. Uchida,M. Arai,H. Tomoda,S. ōmura.Phoma sp. FOM-8108, a producer of gentisylquinones, isolated from sea sand[J].Mycoscience.2002(2)
  • 6Byeng Wha Son,Jung Chul Kim,Hong Dae Choi,Jung Sook Kang.A radical scavenging Farnesylhydroquinone from a marine-derived fungusPenicillium sp.[J].Archives of Pharmacal Research.2002(1)
  • 7Fenical W. Chemical Reviews . 1993
  • 8Thomson RH. Naturally Occurring Quinines . 1987
  • 9Matsushita MA,Matsuo M,Koga Y,et al. Int J Sys Bac-teriol . 1992
  • 10Rodriguez AD. Tetrahedron . 1990

二级参考文献11

  • 1Faulkner, D. J. Nat. Prod. Rep. 2001, 18, 1.
  • 2Lin, Y. C. Shao, Z. Y. Jiang, G. C. Zhou, S. N. Cai,J. Vrijmoed, L. L. P. Jones, E. B. G. Tetrahedron 2000,56(49), 9607.
  • 3Lin, Y. C. Wu, X. Y. Feng, S. Jiang, G. C. Zhou, S.N. Vrijmoed, L. L. P. Jones, E. B. G. Tetrahedron Lett.2001, 42, 449.
  • 4Lin, Y. C. Wu, X. Y. Feng, S. Jiang, G. C. Luo, J.Zhou, S. N. Vrijmoed, L. L. P. Jones, E. B. G. Krohn,K. Steingrover, K. Zsila, F. J. Org. Chem. 2001, 66,6252.
  • 5Gorst-Allman, C. P. Steyn, P. S. Wessels, P. L. J. Chem.Soc., Perkin Trans. 1 1977, 1360.
  • 6Townsend, C. A. Christensen, S. B. Tetrahedron 1983, 39(21), 3575.
  • 7O'Malley, G. J. Murphy, R. A. Cava, M. P. J. Org.Chem. 1985, 50, 5533.
  • 8Hamasaki, T. Hatsuda, Y. Terashima, N. Renbutsu, M.Agric. Biol. Chem. 1967, 31(1), 11.
  • 9胡军,屠鹏飞,果德安,郑俊华.秦岭大黄化学成分研究[J].西北药学杂志,1997,12(4):153-155. 被引量:22
  • 10敏德,徐丽萍,张治针,王弘,黄丹,果德安,郑俊华.天山大黄的化学成分研究(Ⅰ)[J].中国中药杂志,1998,23(7):416-418. 被引量:50

共引文献31

同被引文献88

引证文献5

二级引证文献17

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部