Planta Med 2012; 78(2): 141-147
DOI: 10.1055/s-0031-1280311
Natural Product Chemistry
Original Papers
© Georg Thieme Verlag KG Stuttgart · New York

Lignans from the Flower Buds of Magnolia liliflora Desr.

Wen-Shu Wang1 , Xiao-Cong Lan1 , Hai-Bo Wu1 , Yao-Zhao Zhong1 , Jing Li1 , Ying Liu1 , Cong-Cong Shao1
  • 1College of Life and Environmental Sciences, Minzu University of China, Beijing, P. R. China
Further Information

Publication History

received February 16, 2011 revised Sept. 21, 2011

accepted Sept. 30, 2011

Publication Date:
24 October 2011 (online)

Abstract

Six new lignans, 16, along with six known compounds were obtained from the flower buds of Magnolia liliflora Desr. The new lignans were elucidated as (1S*,2R*,5S*,6S*)-2-(3,5-dimethoxyphenyl)-6-(3,4-methylenedioxyphenyl)-3,7-dioxabicyclo[3.3.0]octane (1), (1R*,2R*,5R*,6S*)-2-(3,5-dimethoxyphenyl)-6-(3,4-methylenedioxyphenyl)-3,7-dioxabicyclo[3.3.0]octane (2), (1R*, 2R*,5R*,6S*)-2,6-bis (3,5-dimethoxyphenyl)-3,7-dioxabicyclo[3.3.0]octane (3), (1R*,2S*,5R*,6R*)-2-(3,4-methylenedioxyphenyl)-6-(3,5-dimethoxyphenyl)-3,7-dioxabicyclo[3.3.0]octane (4), (7′S*,8R*,8′R*)-3,5′-dimethoxy-3′,4,9′-trihydroxy-7′, 9-epoxy-8,8′-lignan (5), and (7′R*,8′S*)-3,3′,4,5′-tetramethoxy-7-en-7′,9-epoxy-8,8′-lignan (6), by the analysis of 1D and 2D-NMR as well as HRESIMS data. The capacity of compound 1 to protect against damages to the DNA of rat lymphocyte cells induced by UV irradiation was assessed by the comet assay. It showed stronger antigenotoxicity than ascorbic acid from 6 × 10−3 mmol · L−1 to 6 × 10−6 mmol · L−1.

Supporting Information

References

  • 1 Liu Y H, Luo X R, Wu Y F. Flora of China. Vol. 30: Menispermaceae, Magnoliaceae. Beijing: Science Press; 1996: 140-141
  • 2 Jung K Y, Kim D S, Oh S R, Park S H, Lee I S, Lee J J, Shin D H, Lee H K. Magnone A and B, novel anti-PAF tetrahydrofuran lignans from the flower buds of Magnolia fargesii.  J Nat Prod. 1998;  61 808-811
  • 3 Ho K Y, Tsai C C, Chen C P, Huang J S, Lin C C. Antimicrobial activity of honokiol and magnolol isolated from Magnolia officinalis.  Phytother Res. 2001;  15 139-141
  • 4 Syu W J, Shen C C, Lu J J, Lee G H, Sun C M. Antimicrobial and cytotoxic activities of neolignans from Magnolia officinalis.  Chem Biodivers. 2004;  1 530-537
  • 5 Youn U J, Chen Q C, Jin W Y, Lee I S, Kim H J, Lee J P, Chang M J, Min B S, Bae K H. Cytotoxic lignans from the stem bark of Magnolia officinalis.  J Nat Prod. 2007;  70 1687-1689
  • 6 Li D Q. Pharmacopoeia of the P.R.C. Beijing: Chemical and Technologic Press; 2005: 126-127
  • 7 Tice R R, Agurell E, Anderson D, Burlinson B, Hartmann A, Kobayashi H, Miyamae Y, Rojas E, Ryu J C, Sasaki Y. The single cell gel/comet assay: guidelines for in vitro and in vivo genetic toxicology testing.  Env Mol Mutagen. 2000;  35 206-221
  • 8 Kimura T, Sonoda Y, Iwai N, Satoh M, Yamaguchi M, Izui T, Suda M, Sasaki K, Nakano T. Proliferation and cell death of embryonic primitive erythrocytes.  Exp Hematol. 2000;  28 635-641
  • 9 Yu P, Wang X L, Yan Q C. Study on protection of procyanidins against UV-induced oxidative damage of lens epitheliaI cells.  Int J Ophthalmol. 2010;  10 1477-1480
  • 10 Lyons N M, O'Brien N M. Modulatory effects of an algal extract containing astaxanthin on UVA-irradiated cells in culture.  J Dermatol Sci. 2002;  30 73-84
  • 11 Singh N P, McCoy M T, Tice R R, Schneider E L. A simple technique for quantitation of low levels of DNA damage in individual cells.  Exp Cell Res. 1988;  175 184-191
  • 12 Agner A R, Bazo A P, Ribeiro L R, Salvadori D M. DNA damage and aberrant crypt foci as putative biomarkers to evaluate the chemopreventive effect of annatto (Bixa orellana L.) in rat colon carcinogenesis.  Mutat Res. 2005;  582 146-154
  • 13 Méndez-Robles M D, Permady H H, Jaramillo-Flores M E, Lugo-Cervantes E C, Cardador-Martínez A, Canales-Aguirre A A, López-Dellamary F, Cerda-García-Rojas C M, Tamariz J. C-26 and C-30 apocarotenoids from seeds of Ditaxis heterantha with antioxidant activity and protection against DNA oxidative damage.  J Nat Prod. 2006;  69 1140-1144
  • 14 Chen C C, Huang Y L, Chen H T, Chen Y P, Hsu H Y. On the calcium-antagonistic principles of the flower buds of Magnolia fargesii.  Planta Med. 1988;  54 438-440
  • 15 Seo S M, Lee H J, Lee O K, Jo H J, Kang H Y, Choi D H, Paik K H, Khan M. Furofuran lignans from the bark of Magnolia kobus.  Chem Nat Comp. 2008;  44 419-423
  • 16 Miyazawa M, Kasahara H, Kameoka H. Biotransformation of lignans: metabolism of (+)-eudesmin and (+)-magnolin in Spodoptera litura.  Phytochemistry. 1995;  39 1027-1030
  • 17 Yang G Z, Hu Y, Yang B, Chen Y. Lignans from the bark of Zanthoxylum planispinum.  Helv Chim Acta. 2009;  92 1657-1664
  • 18 Xie L H, Akao T, Hamasaki K, Deyama T, Hattori M. Biotransformation of pinoresinol diglucoside to mammalian lignans by human intestinal microflora, and isolation of Enterococcus faecalis strain PDG-1 responsible for the transformation of (+)-pinoresinol to (+)-lariciresinol.  Chem Pharm Bull. 2003;  51 508-515
  • 19 Xu R S, Ye Y, Zhao W M. Introduction to Natural Products Chemistry. Beijing: Science Press; 2006: 318-320
  • 20 Kakisawa H, Chen Y P, Hsij H Y. Lignans in flower buds of Magnolia fargesii.  Phytochemistry. 1972;  11 2289-2293
  • 21 Yoshida S, Yamanaka T, Miyake T, Moritani Y, Ohmizu H, Iwasaki T. Asymmetric syntheses of lignans utilizing novel diastereoselective Michael addition of cyanohydrin: syntheses of (+)-fargesin and (−)-picropodophyllone.  Tetrahedron. 1997;  53 9585-9598
  • 22 Mustafayeva K, Di Giorgio C, Elias R, Kerimov Y, Ollivier E, De Méo M. DNA-damaging, mutagenic, and clastogenic activities of gentiopicroside isolated from Cephalaria kotschyi roots.  J Nat Prod. 2010;  73 99-103

Dr. Wen-Shu Wang

College of Life and Environmental Sciences
Minzu University of China

Zhongguancun South Avenue 27#

Beijing 100081

P. R. China

Phone: +86 10 68 93 22 42

Fax: +86 10 68 93 69 27

Email: wangws@muc.edu.cn