期刊文献+

Phakellia属海绵次生代谢产物研究进展 被引量:2

Research progress on secondary metabolites from marine sponge of genus Phakellia
原文传递
导出
摘要 海绵是目前海洋天然产物研究中最吸引人的海洋生物之一,海绵中含有丰富的、结构新颖的次生代谢产物,大多数具有显著的生理活性。Phakellia属海绵属于寻常海绵纲软海绵目小轴海绵科,种类较多,分布广泛,在国内外得到了广泛的研究。对近几十年来从Phakellia属海绵中分离鉴定的次生代谢产物进行了系统的归纳整理,这些化学成分主要包括环肽、生物碱、聚醚、萜类、甾醇、炔酸等种类,并对其药理活性进行了简单总结,对Phakellia属海绵的进一步研究开发具有一定的借鉴和指导意义。 Marine sponge is one of the most attractive marine organism on the research of marine natural products. Sponge contains abundant new secondary metabolites, most of which have significant biological activities. Phakellia spp., belonging to Axinellidae, Halichondrida, Demospongiae, is widely distributed at home and abroad, and it has been widely studied. This paper reviews the progress in the chemical and biological activities of the secondary metabolites from the sponge of genus Phakellia spp. in the past decades. The secondary metabolites mainly include cyclic peptide, alkaloids, polyether, terpenoids, sterols, and acetylenic acids. This paper is meaningful to the further research and development of marine sponge Phakellia spp.
出处 《药物评价研究》 CAS 2012年第2期130-135,共6页 Drug Evaluation Research
关键词 海绵 Phakellia 次生代谢产物 环肽 marine sponge Phakellia secondary metabolites cyclic peptide
  • 相关文献

参考文献8

二级参考文献21

  • 1贺焕华,徐石海,曾向潮.吡咯并内酰胺生物碱:2- 溴-6 ,7-二氢-1H ,5H-吡咯并[2,3-C]氮杂-4 ,8-二酮的X-ray晶体结构研究(英文)[J].天然产物研究与开发,2002,14(4):1-4. 被引量:2
  • 2徐效华,姚广民,卢建华,李艳明,林长江.海绵Phacelliafusca Schmidt中一个结构新颖的脑甙类化合物[J].高等学校化学学报,2001,22(z1):116-119. 被引量:1
  • 3ZENG,Long-Mei FU,Xiong SU,Jing-Yu Department of Chemistry,Zhongshan University,Guangzhou 510275De GUZMAN,Florecita SCHMITZ,Francis J HOSSAIN,M.Bilayet van der HELM,Dick Department of Chemistry and Biochemistry,University of Oklahoma,Norman,OK73019-0370,U.S.A..Studies on the chemical constituents of the South China Sea sponge Phacellia fusca[J].Chinese Journal of Chemistry,1991,9(2):136-143. 被引量:1
  • 4邓松之,李凤英,谈燮峰,何直升.南海柳珊瑚Isis sp.化学成分的研究[J].天然产物研究与开发,1994,6(4):9-11. 被引量:30
  • 5[1]Kitagawa I, Kobayashi M, Kitanaka K, Kido M, Kyogoku Y. Marine natural products Ⅻ. On the chemical constituents of the Okinawan marine sponge Hymeniacidon alidis. Chem. Pharm . Bull. , 1983,31:2321
  • 6[2]Kobayashi,J,Ohizumi Y,Nakamura H,Hirata Y,Wakamatsu K, Miyazawa T. Hemenin, a novel a-adrenoceptor blocking agent from the Okinawan marine sponge Hymeniacidan sp.. Experientia, 1986,42(9): 1064~ 1065
  • 7[3]Albizati K F, Faulkner D J. Stevensine, a novel alkaloid of an unidentified marine sponge. J. Org. Chem, 1985,50: 4163
  • 8[4]Hirokazu A, Toshio T. Total synthesis of hymenialdisin and debromohymenialdisin: sterospecific construction of the 2-amino-4-oxo-2-imidazolin-5 (Z)-disubstituted ylidene ring system. Tetrahedron Lett., 1995,36: 413~ 416
  • 9[5]Xu Y, Phan G, Yakushijin K, Horne D A. A synthesis of (±)-hymenin. Tetrahedron Lett. , 1994,35:351
  • 10[6]Mattia C A, Mazzarella L, Puliti R. 4- (2-amino-4-oxo-2-imi-dazolin-5-ylidene)-2-bromo-4, 5, 6, 7-tetrahydropyrrolo [ 2,3-c]azepin-8-one methanol solvate: a new bromo compound from the sponge Acanthella Aurantiaca. Acta Cryst..B38,1982,2513 ~ 2515

共引文献27

同被引文献39

  • 1唐生安,邓志威,李军,付宏征,裴月湖,林文翰.南海海绵Jaspis sp.中的异臭椿类三萜成分[J].中国天然药物,2005,3(4):213-218. 被引量:2
  • 2曾向潮,徐石海,李毅群,刘珀润,李玉霞.N-(溴代-2-吡咯甲酰基)氨基酸甲酯的合成[J].有机化学,2005,25(11):1420-1426. 被引量:2
  • 3张浩,靳艳,张卫.南海海绵Axinella sp.中两个含吡咯七元环内酰胺生物碱的分离鉴定[J].中药材,2006,29(12):1299-1301. 被引量:3
  • 4Aratake S, Trianto A, Hanif N, et al. A new polyunsaturated brominated fatty acid from a Haliclona sponge [J]. Mar Drugs, 2009, 7(4): 523-527.
  • 5Watanabe K, Tsuda Y, Yamane Y, et al. Strongylodiols A, B and C, new cytotoxic cetylenic alcohols isolated from the Okinawan marine sponge of the genus Strongylophora as each enantiomeric mixture with adifferent ratio [J]. Tetrahedmn Lett, 2000, 41(48): 9271-9276.
  • 6Ernesto F,. Taglialatela-Scafati O, Di Rosa M, et al. Metabolites from the sponge Plakortis simplex. Part 3: Isolation and stereostructure of novel bioactive cycloperoxides and diol analogues [J]. Tetruhedron, 2000,56(40): 7959-7967.
  • 7Dai J, Liu Y, Zhou Y D, et al. Hypoxia-selective antitumor agents: norsesterterpene peroxides fi'om the marine sponge Diacarnus levii preferentially suppress the growth of tumor cells under hypoxic conditions [J]. J Nat Prod, 2007, 70(1):130-133.
  • 8Johnson T A, Tenney K, Cichewicz R H, et al. Sponge-derived fijianolide polyketide class: further evaluation of their structural and cytotoxicity properties [J]. JMed Chem, 2007, 50(16): 3795-3803.
  • 9Chevallier C, Bugni T S, Feng X, et al. Tedanolide C: a potent new 18-membered ring cytotoxic macrolide isolated from the Papua New Guinea marine sponge lrcinia sp. [J]. J Org Chem, 2006, 71(6): 2510-2513.
  • 10Singh A J, Xu C X, Xu X, et al. Peloruside B, a potent antitumor macrolide from the New Zealand marine sponge Mycale hentscheli: isolation, structure, total synthesis, and bioactivity [J]. JOrg Chem, 2010, 75(1): 2-10.

引证文献2

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