Planta Med 2007; 73(11): 1202-1207
DOI: 10.1055/s-2007-981596
Natural Product Chemistry
Original Paper
© Georg Thieme Verlag KG Stuttgart · New York

Flavonoids from Acacia pennata and their Cyclooxygenase (COX-1 and COX-2) Inhibitory Activities

Alain B. Dongmo1 , Tomofumi Miyamoto2 , Kazuko Yoshikawa3 , Shigenobu Arihara3 , Marie-Aleth Lacaille-Dubois1
  • 1Faculté de Pharmacie, Laboratoire de Pharmacognosie, Unité de Molécules d’Intérêt Biologique, UMIB, UPRES-EA 3660, Université de Bourgogne, Dijon, France
  • 2Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan
  • 3Faculty of Pharmaceutical Sciences, Tokushima Bunri University, Yamashiro-Cho, Tokushima, Japan
Further Information

Publication History

Received: December 22, 2006 Revised: July 12, 2007

Accepted: July 16, 2007

Publication Date:
07 September 2007 (online)

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Abstract

Two new flavonoids quercetin 4′-O-α-L-rhamnopyranosyl-3-O-ß-D-allopyranoside (1) and apigenin 6-C-[2′′-O-(E)-feruloyl-β-D-glucopyranosyl]-8-C-β-glucopyranoside (2), along with the known isorhamnetin 3-O-α-L-rhamnopyranoside (3), kaempferol 3-O-α-L-rhamnopyranosyl-(1→4)-β-D-glucopyranoside (4), and isovitexin (5) were isolated from the leaves of Acacia pennata Willd. (Mimosaceae) and tested for their anti-inflammatory activity. Their structures were determined by 1D and 2D NMR and mass spectrometry. They were tested for an inhibitory effect on COX-1 and COX-2, showing 60 - 90 % inhibition at 10 - 4 g/mL and 5 - 14 % inhibition at 10 - 4 g/mL, respectively.

References

Prof. Marie-Aleth Lacaille-Dubois

Faculté de Pharmacie

Laboratoire de Pharmacognosie

Unité de Molécules d’Intérêt Biologique UMIB

UPRES-EA 3660

Université de Bourgogne

7 Bd. Jeanne d’Arc

BP 87900

21079 Dijon Cedex

France

Phone: +33-3-8039-3229

Fax: +33-3-8039-3474

Email: m-a.lacaille-dubois@u-bourgogne.fr