Planta Med 2005; 71(7): 654-658
DOI: 10.1055/s-2005-871272
Original Paper
Natural Product Chemistry
© Georg Thieme Verlag KG Stuttgart · New York

Brosimacutins J - M, Four New Flavonoids from Brosimum acutifolium and their Cytotoxic Activity

Junko Takashima1 , Kanki Komiyama2 , Haruaki Ishiyama3 , Jun’ichi Kobayashi3 , Ayumi Ohsaki4
  • 1Research & Development Division, Mitsubishi Pharma Corporation, Yokohama, Japan
  • 2The Kitasato Institute, Tokyo, Japan
  • 3Graduate School of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan
  • 4Institute of Biomaterials and Bioengineering, Tokyo Medical and Dental University, Tokyo, Japan
Further Information

Publication History

Received: September 2, 2004

Accepted: January 5, 2005

Publication Date:
18 July 2005 (online)

Abstract

Four new flavonoids, brosimacutins J - M (1 - 4), were isolated from the bark of Brosimum acutifolium Huber together with a known flavan, brosimine A (5). The structures of compounds 1 - 4 were elucidated by spectroscopic means. 27 constituents of this plant including compounds 1 - 5 were evaluated for their cytotoxic activity against murine leukemia P388 cells. Although no compounds tested had any reversal effect on vincristine resistance, brocimacutins J - M (1 - 4) were cytotoxic to vincristine-resistant P388 cells (IC50 4.4 - 19 μg/mL).

References

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Junko Takashima

Research & Development Division

Mitsubishi Pharma Corporation

1000 Kamoshida-cho

Aoba-ku

Yokohama 227-0033

Japan

Fax: +81-45-963-4211

Email: Takashima.Junko@me.m-pharma.co.jp

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