期刊文献+

Isolation, identification, and cytotoxicity of a new isobenzofuran derivative from marine Streptomyces sp. W007 被引量:1

Isolation, identification, and cytotoxicity of a new isobenzofuran derivative from marine Streptomyces sp. W007
下载PDF
导出
摘要 A new isobenzofuran derivative( 1) was isolated from the marine Streptomyces sp. W007 and its structure was determined through extensive spectroscopic analyses, including 1D-NMR, 2D-NMR, and ESI-MS. The absolute configuration of compound 1 was determined by a combination of experimental analyses and comparison with reported data, including biogenetic reasoning, J-coupling analysis, NOESY, and 1 H- 1 HCOSY. Compound 1 exhibited no cytotoxicity against human cells of gastric cancer BGC-823, lung cancer A549, and breast cancer MCF7. A new isobenzofuran derivative (1) was isolated from the marine Streptomyces sp. W007 and its structure was determined through extensive spectroscopic analyses, including 1D-NMR, 2D-NMR, and ESI-MS. The absolute configuration of compound 1 was determined by a combination of experimental analyses and comparison with reported data, including biogenetic reasoning, J-coupling analysis, NOESY, and 1H-1HCOSY. Compound 1 exhibited no cytotoxicity against human cells of gastric cancer BGC-823, lung cancer A549, and breast cancer MCF7.
出处 《Chinese Journal of Oceanology and Limnology》 SCIE CAS CSCD 2016年第2期386-390,共5页 中国海洋湖沼学报(英文版)
基金 Supported by the Open Fund of Key Laboratory of Experimental Marine Biology,Chinese Academy of Sciences(No.KF2015No07) the Innovative and Entrepreneurial Training Program of College Students,Tianjin University of Commerce(No.2015052)
关键词 marine streptomycete isobenzofuran derivative absolute configuration CYTOTOXICITY 海洋链霉菌 生物毒性 苯并呋喃 分离测定 BGC-823 鉴定 ESI-MS 细胞毒性
  • 相关文献

参考文献15

  • 1Barfield M, Spear R J, Sternhell S. 1975. Interproton spin-spin coupling across a dual path in 2, 5-dihydrofurans and phthalans. J. Am. Chem. Soc., 97 (18): 5160–5167.CrossRef.
  • 2Bérdy J. 2005. Bioactive microbial metabolites. J. Antibiot., 58 (1): 1–26.CrossRef.
  • 3Fotso S, Mahmud T, Zabriskie T M et al. 2008. Rearranged and unrearranged angucyclinones from Indonesian Streptomyces spp. J. Antibiot., 61 (7): 449–456.CrossRef.
  • 4Harper J K, Arif A M, Ford E J, Strobel G A, Porco J A Jr, Tomer D P, Oneill K L, Heider E M, Grant D M. 2003. Pestacin: a 1, 3-dihydro isobenzofuran from Pestalotiopsis microspora possessing antioxidant and antimycotic activities. Tetrahedron, 59 (14): 2471–2476.CrossRef.
  • 5Puder C, Zeeck A, Beil W. 2000. New biologically active rubiginones from Streptomyces sp. J. Antibiot., 53 (4): 329–336.CrossRef.
  • 6Sasaki T, Yoshida J, Itoh M, Gomi S, Shomura T, Sezaki M. 1988. New antibiotics SF2315A and B produced by an Excellospora sp. I. Taxonomy of the strain, isolation and characterization of antibiotics. J. Antibiot., 41 (7): 835–842.
  • 7Solanki R, Khanna M, Lal R. 2008. Bioactive compounds from marine actinomycetes. Indian J. Microbiol., 48 (4): 410–431.CrossRef.
  • 8Strobel G, Ford E, Worapong J, Harper J K, Arif A M, Grant D M, Fung P C W, Chau R M W. 2002. Isopestacin, an isobenzofuranone from Pestalotiopsis microspora, possessing antifungal and antioxidant activities. Phytochemistry, 60 (2): 179–183.CrossRef.
  • 9Tsukuda E, Tanaka T, Ochiai K, Kondo H, Yoshida M, Agatsuma T, Saitoh Y, Teshiba S, Matsuda Y. 1996. EI-1507-1 and-2, novel interleukin-1 ? converting enzyme inhibitors produced by Streptomyces sp. E-1507. J. Antibiot., 49 (4): 333–339.
  • 10Wang H B, Li H Y, Zuo M X, Zhang Y, Liu H, Fang W S, Chen X G. 2008. Lx2-32c, a novel taxane and its antitumor activities in vitro and in vivo. Cancer Lett., 268 (1): 89–97.CrossRef.

同被引文献10

引证文献1

二级引证文献1

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