Planta Med 2003; 69(3): 241-246
DOI: 10.1055/s-2003-38485
Original Paper
Natural Product Chemistry
© Georg Thieme Verlag Stuttgart · New York

New Adjacent Bis-Tetrahydrofuran Annonaceous Acetogenins from Annona muricata

Fang-Rong Chang1 , Chih-Chuang Liaw1 , Chih-Yuan Lin1 , Chi-Jung Chou1 , Hui-Fen Chiu1 , Yang-Chang Wu1
  • 1Graduate Institute of Natural Products, Kaohsiung Medical University, Kaohsiung, Taiwan, R.O.C.
Further Information

Publication History

Received: June 25, 2002

Accepted: November 16, 2002

Publication Date:
04 April 2003 (online)

Abstract

Bioactivity-guided fractionation led to the isolation of two new Annonaceous acetogenins, annocatacin A (1) and annocatacin B (2), from the seeds and the leaves, respectively, of Annona muricata. Compounds 1 and 2 are the first examples where the adjacent bis-tetrahydrofuran ring system is located at C-15. The new structures were elucidated and characterized by spectral and chemical methods. Both Annonaceous acetogenins 1 and 2 showed significant in vitro cytotoxicity toward the human hepatoma cell lines, Hep G2 and 2,2,15, and were compared with the known adjacent bis-tetrahydrofuran acetogenins, neoannonin (3), desacetyluvaricin (4), bullatacin (5), asimicin (6), annoglaucin (7), squamocin (8), and rollimusin (9).

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Prof. Dr. Yang-Chang Wu

Graduate Institute of Natural Products

Kaohsiung Medical University

Kaohsiung 807

Taiwan

Republic of China

Fax: +886-7-3114773

Email: yachwu@kmu.edu.tw

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