Planta Med 2005; 71(2): 153-159
DOI: 10.1055/s-2005-837783
Original Paper
Natural Product Chemistry
© Georg Thieme Verlag KG Stuttgart · New York

Digoniodiol, Deoxygoniopypyrone A, and Goniofupyrone A: Three New Styryllactones from Goniothalamus amuyon

Yu-Hsuan Lan1 , Fang-Rong Chang1 , Chih-Chuang Liaw1 , Chin-Chung Wu1 , Michael-Y Chiang2 , Yang-Chang Wu1
  • 1Graduate Institute of Natural Products, Kaohsiung Medical University, Kaohsiung, Taiwan
  • 2Department of Chemistry, National Sun Yat-Sen University, Kaohsiung, Taiwan
Further Information

Publication History

Received: April 26, 2004

Accepted: August 29, 2004

Publication Date:
24 February 2005 (online)

Abstract

Three new styrylpyrone analogues, digoniodiol (2), deoxygoniopypyrone A (3), and goniofupyrone A (4), along with ten known styryllactones, were isolated from the aerial parts of Goniothalamus amuyon. Among these compounds, 2 is the first example of a bis-styrylpyrone. Compound 4 represents a new skeleton for styryllactones. All structures were established on the basis of spectroscopic data. The stereochemistry of 2 and 4 was determined by X-ray crystallographic analysis. The absolute configuration of 3 and 4 was further confirmed by Mosher ester derivatives. All styryllactones were subjected to cytotoxicity assays. Among them, goniothalamin, goniothalamin epoxide, and 8-chlorogoniodiol showed significant cytotoxicity against the HepG2 cancer cell line with IC50 in the range of 0.19 - 0.64 μg/mL, and moderate activity toward Hep3B, MDA-MB-231, and MCF-7 cancer cell lines.

References

  • 1 Bermejo A, Lora M J, Blázquez M A, Rao K S, Cortes D, Zafra-Polo M C. (+)-Goniotharvensin, a new styryl-lactone from the stem bark of Goniothalamus arvensis .  Nat Prod Lett. 1995;  7 117-22
  • 2 Kan W S. Pharmaceutical Botany. National Research Institute of Chinese Medicine Taipei; 1979: p 247
  • 3 Surivet J P, Vatèle J M. Total synthesis of antitumor Goniothalamus styryllactones.  Tetrahedron. 1999;  55 13 011-28
  • 4 Blázquez M A, Bermejo A, Zafra-Polo M C, Cortes D. Styryl-lactones from Goniothalamus species - a review.  Phytochem Anal. 1999;  4 161-70
  • 5 Wu Y C, Duh C Y, Chang F R, Chang G Y. The crystal structure and cytotoxicity of goniodiol 7-monoacetate from Goniothalamus amuyon .  J Nat Prod. 1991;  54 1077-81
  • 6 Wu Y C, Chang F R, Duh C Y, Wang S K, Wu T S. Cytotoxic styrylpyrones of Goniothalamus amuyon .  Phytochemistry. 1992;  31 2851-3
  • 7 Lan Y H, Chang F R, Yu J H, Yang Y L, Chang Y L, Lee S J, Wu Y C. Cytotoxic styrylpyrones from Goniothalamus amuyon .  J Nat Prod. 2003;  66 487-90
  • 8 Cavalheiro A J, Yoshida M. 6-[ω-Arylalkenyl]-5,6-dihydro-α-pyrones from Cryptocarya moschata (Lauraceae).  Phytochemistry. 2000;  53 811-9
  • 9 Sam T W, Chew S Y, Matsjeh S, Gan E K, Razak D, Mohamed A L. Goniothalamin oxide: an embryotoxic compound from Goniothalamus macrophyllus (Annonaceae).  Tetrahedron Lett. 1987;  28 2541-4
  • 10 Talapatra S K, Basu D, Deb T, Goswami S, Talapatra B. Structure and stereochemistry of four new 5,6-dihydro-2-pyrones from Goniothalamus sesquipedalis and Goniothalamus grifithii .  Ind J Chem. 1985;  24B 29-34
  • 11 Fang X P, Anderson J E, Chang C J, McLaughlin J L. Two new styryllactones, 9-deoxygoniopypyrone and 7-epi-goniofufurone, from Goniothalamus giganteus .  J Nat Prod. 1991;  54 034-43
  • 12 Fang X P, Anderson J E, Chang C J, McLaughlin J L. Three new bioactive styryllactones from Goniothalamus giganteus (Annonaceae).  Tetrahedron. 1991;  47 9751-8
  • 13 Elliott W M, Auersperg N. Comparison of the neutral red and methylene blue assays to study cell growth in culture.  Biotech Histochem. 1993;  68 29-35
  • 14 Talapatra B, Porel A, Biswas K, Talapatra S K. Absolute configurations of goniodiol, goniodiol monoacetate and other related dihydropyrones from synthetic, circular dichroism and X-ray crystallographic evidence.  J Indian Chem Soc. 1997;  74 896-903
  • 15 Wang S, Zhang Y J, Chen R Y, Yu D Q. Goniolactones A-F, six new styrylpyrone derivatives from the roots of Goniothalamus cheliensis .  J Nat Prod. 2002;  65 835-841

Prof. Dr. Yang-Chang Wu

Graduate Institute of Natural Products

Kaohsiung Medical University

Kaohsiung 807

Taiwan

Republic of China

Fax: +886-7-311-4773

Email: yachwu@kmu.edu.tw

    >