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Senedensiscins A-F: six new eudesmane sesquiterpenoid glucosides from Senecio densiserratus

To link to full-text access for this article, visit this link: http://dx.doi.org/10.1016/j.tet.2013.10.047 Byline: Jian-Jun Chen, Hong-Bo Wei, Yuan-Zhen Xu, Shu-Chen Hu, Kun Gao Abstract: Six new highly oxygenated eudesmane sesquiterpenoid glucosides, senedensiscins A-F (1-6), were isolated from the... Full description

Journal Title: Tetrahedron Dec 9, 2013, Vol.69(49), p.10598(6)
Main Author: Chen, Jian - Jun
Other Authors: Wei, Hong - Bo , Xu, Yuan - Zhen , Hu, Shu - Chen , Gao, Kun
Format: Electronic Article Electronic Article
Language: English
Subjects:
Quelle: Cengage Learning, Inc.
ID: ISSN: 0040-4020
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recordid: gale_ofa349014485
title: Senedensiscins A-F: six new eudesmane sesquiterpenoid glucosides from Senecio densiserratus
format: Article
creator:
  • Chen, Jian - Jun
  • Wei, Hong - Bo
  • Xu, Yuan - Zhen
  • Hu, Shu - Chen
  • Gao, Kun
subjects:
  • Glucosides -- Analysis
ispartof: Tetrahedron, Dec 9, 2013, Vol.69(49), p.10598(6)
description: To link to full-text access for this article, visit this link: http://dx.doi.org/10.1016/j.tet.2013.10.047 Byline: Jian-Jun Chen, Hong-Bo Wei, Yuan-Zhen Xu, Shu-Chen Hu, Kun Gao Abstract: Six new highly oxygenated eudesmane sesquiterpenoid glucosides, senedensiscins A-F (1-6), were isolated from the aerial parts of Senecio densiserratus. Their structures with the absolute configurations were established on the basis of spectroscopic analyses and chemical methods. These compounds represent an unprecedented type of sesquiterpenoid glucoside with the angeloyl group directly connected to the glucosyl moiety and their cytotoxicity was evaluated against the selected human cell lines, HL-60, SMMC-7721, and HeLa. Author Affiliation: State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000, People's Republic of China Article History: Received 26 July 2013; Revised 27 September 2013; Accepted 14 October 2013
language: English
source: Cengage Learning, Inc.
identifier: ISSN: 0040-4020
fulltext: fulltext
issn:
  • 0040-4020
  • 00404020
url: Link


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titleSenedensiscins A-F: six new eudesmane sesquiterpenoid glucosides from Senecio densiserratus
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descriptionTo link to full-text access for this article, visit this link: http://dx.doi.org/10.1016/j.tet.2013.10.047 Byline: Jian-Jun Chen, Hong-Bo Wei, Yuan-Zhen Xu, Shu-Chen Hu, Kun Gao Abstract: Six new highly oxygenated eudesmane sesquiterpenoid glucosides, senedensiscins A-F (1-6), were isolated from the aerial parts of Senecio densiserratus. Their structures with the absolute configurations were established on the basis of spectroscopic analyses and chemical methods. These compounds represent an unprecedented type of sesquiterpenoid glucoside with the angeloyl group directly connected to the glucosyl moiety and their cytotoxicity was evaluated against the selected human cell lines, HL-60, SMMC-7721, and HeLa. Author Affiliation: State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000, People's Republic of China Article History: Received 26 July 2013; Revised 27 September 2013; Accepted 14 October 2013
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descriptionTo link to full-text access for this article, visit this link: http://dx.doi.org/10.1016/j.tet.2013.10.047 Byline: Jian-Jun Chen, Hong-Bo Wei, Yuan-Zhen Xu, Shu-Chen Hu, Kun Gao Abstract: Six new highly oxygenated eudesmane sesquiterpenoid glucosides, senedensiscins A-F (1-6), were isolated from the aerial parts of Senecio densiserratus. Their structures with the absolute configurations were established on the basis of spectroscopic analyses and chemical methods. These compounds represent an unprecedented type of sesquiterpenoid glucoside with the angeloyl group directly connected to the glucosyl moiety and their cytotoxicity was evaluated against the selected human cell lines, HL-60, SMMC-7721, and HeLa. Author Affiliation: State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000, People's Republic of China Article History: Received 26 July 2013; Revised 27 September 2013; Accepted 14 October 2013
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abstractTo link to full-text access for this article, visit this link: http://dx.doi.org/10.1016/j.tet.2013.10.047 Byline: Jian-Jun Chen, Hong-Bo Wei, Yuan-Zhen Xu, Shu-Chen Hu, Kun Gao Abstract: Six new highly oxygenated eudesmane sesquiterpenoid glucosides, senedensiscins A-F (1-6), were isolated from the aerial parts of Senecio densiserratus. Their structures with the absolute configurations were established on the basis of spectroscopic analyses and chemical methods. These compounds represent an unprecedented type of sesquiterpenoid glucoside with the angeloyl group directly connected to the glucosyl moiety and their cytotoxicity was evaluated against the selected human cell lines, HL-60, SMMC-7721, and HeLa. Author Affiliation: State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000, People's Republic of China Article History: Received 26 July 2013; Revised 27 September 2013; Accepted 14 October 2013
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