Phytochemicals from the stem wood of Sorbus lanata (D. Don.) Schauer

Research output: Contribution to journalArticleResearchpeer review

Authors

  • Ghias Uddin
  • Abdul Latif
  • Mohammad Arfan
  • Mumtaz Ali
  • Syed Hamid Hussain
  • Thomas J. Simpson
  • Russel J. Cox
  • Muhammad Iqbal Choudhary

External Research Organisations

  • University of Peshawar
  • University of Malakand
  • University of Bristol
  • University of Karachi
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Details

Original languageEnglish
Pages (from-to)84-89
Number of pages6
JournalPhytochemistry letters
Volume6
Issue number1
Publication statusPublished - 1 Feb 2013
Externally publishedYes

Abstract

Three new phenolic compounds, sorlanin (4-(3-(hydroxymethyl)-5-methoxy-7- phenyl-2,3-dihydrobenzo[b][1,4]dioxin-2-yl)-2-methoxyphenol, 1), sorbanin (2-((3,5-dimethoxy-[1,1′-biphenyl]-4-yl)oxy)-1-(4-hydroxy-3-methoxyphenyl) propane-1,3-diol, 2) and sorbalanin (4-(3-(hydroxymethyl)-5,6-dimethoxy-2,3- dihydrobenzo[b][1,4]dioxino[2,3-g]benzofuran-2-yl)-2-methoxyphenol, 3), together with eight known compounds, polystachyol (4), isolariciresinol (5), dihydrodehydrodiconiferyl alcohol (6), tuberculatin (7), ovafolinin E (8), aucuparin (9), 2′-methoxyaucuparin (10), and tetracosyl-3-(3,4- dihydroxyphenyl)acrylate (11), were isolated from Sorbus lanata. The structures of these phytoconstituents were elucidated through extensive spectroscopic techniques, including UV, IR, 1D and 2D NMR, ESI-MS and HRESI-MS experiments. All the compounds except 9 and 10 were isolated for the first time from the genus Sorbus. The isolated compounds were also tested in DPPH radical scavenging reaction where compounds 6, 7, 10 and 11 showed significant activities with IC50 values of 9.2, 11.7, 23.0 and 33.7 μM, respectively.

Keywords

    DPPH radical scavenging activity, HPLC separations, Phenolic compounds, Sorbus lanata

ASJC Scopus subject areas

Cite this

Phytochemicals from the stem wood of Sorbus lanata (D. Don.) Schauer. / Uddin, Ghias; Latif, Abdul; Arfan, Mohammad et al.
In: Phytochemistry letters, Vol. 6, No. 1, 01.02.2013, p. 84-89.

Research output: Contribution to journalArticleResearchpeer review

Uddin, G, Latif, A, Arfan, M, Ali, M, Hussain, SH, Simpson, TJ, Cox, RJ & Choudhary, MI 2013, 'Phytochemicals from the stem wood of Sorbus lanata (D. Don.) Schauer', Phytochemistry letters, vol. 6, no. 1, pp. 84-89. https://doi.org/10.1016/j.phytol.2012.10.002
Uddin, G., Latif, A., Arfan, M., Ali, M., Hussain, S. H., Simpson, T. J., Cox, R. J., & Choudhary, M. I. (2013). Phytochemicals from the stem wood of Sorbus lanata (D. Don.) Schauer. Phytochemistry letters, 6(1), 84-89. https://doi.org/10.1016/j.phytol.2012.10.002
Uddin G, Latif A, Arfan M, Ali M, Hussain SH, Simpson TJ et al. Phytochemicals from the stem wood of Sorbus lanata (D. Don.) Schauer. Phytochemistry letters. 2013 Feb 1;6(1):84-89. doi: 10.1016/j.phytol.2012.10.002
Uddin, Ghias ; Latif, Abdul ; Arfan, Mohammad et al. / Phytochemicals from the stem wood of Sorbus lanata (D. Don.) Schauer. In: Phytochemistry letters. 2013 ; Vol. 6, No. 1. pp. 84-89.
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title = "Phytochemicals from the stem wood of Sorbus lanata (D. Don.) Schauer",
abstract = "Three new phenolic compounds, sorlanin (4-(3-(hydroxymethyl)-5-methoxy-7- phenyl-2,3-dihydrobenzo[b][1,4]dioxin-2-yl)-2-methoxyphenol, 1), sorbanin (2-((3,5-dimethoxy-[1,1′-biphenyl]-4-yl)oxy)-1-(4-hydroxy-3-methoxyphenyl) propane-1,3-diol, 2) and sorbalanin (4-(3-(hydroxymethyl)-5,6-dimethoxy-2,3- dihydrobenzo[b][1,4]dioxino[2,3-g]benzofuran-2-yl)-2-methoxyphenol, 3), together with eight known compounds, polystachyol (4), isolariciresinol (5), dihydrodehydrodiconiferyl alcohol (6), tuberculatin (7), ovafolinin E (8), aucuparin (9), 2′-methoxyaucuparin (10), and tetracosyl-3-(3,4- dihydroxyphenyl)acrylate (11), were isolated from Sorbus lanata. The structures of these phytoconstituents were elucidated through extensive spectroscopic techniques, including UV, IR, 1D and 2D NMR, ESI-MS and HRESI-MS experiments. All the compounds except 9 and 10 were isolated for the first time from the genus Sorbus. The isolated compounds were also tested in DPPH radical scavenging reaction where compounds 6, 7, 10 and 11 showed significant activities with IC50 values of 9.2, 11.7, 23.0 and 33.7 μM, respectively.",
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AU - Uddin, Ghias

AU - Latif, Abdul

AU - Arfan, Mohammad

AU - Ali, Mumtaz

AU - Hussain, Syed Hamid

AU - Simpson, Thomas J.

AU - Cox, Russel J.

AU - Choudhary, Muhammad Iqbal

N1 - Funding information: We are thankful to the Higher Education Commission of Pakistan for giving financial support through Indigenous 5000 Fellowships Program and International Research Support Initiative Program (IRSIP) to Mr. Abdul Latif (Co-author). We are also grateful to Prof. Tom Simpson, Prof. Russell J. Cox and Prof. Craig Butts of the University of Bristol (UK) for providing technical facilities and guidance throughout the completion of this work.

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Y1 - 2013/2/1

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