Planta Med 2008; 74(1): 80-83
DOI: 10.1055/s-2007-993781
Natural Product Chemistry
Letter
© Georg Thieme Verlag KG Stuttgart · New York

Anthocleistenolide, A New Rearranged Nor-Secoiridoid Derivative from the Stem Bark of Anthocleista vogelii

Mathieu Tene1 , Pierre Tane1 , Jules-Roger Kuiate2 , Jean de Dieu Tamokou2 , Joseph D. Connolly3
  • 1Chemistry Department, University of Dschang, Dschang, Cameroon
  • 2Biochemistry Department, University of Dschang, Dschang, Cameroon
  • 3Chemistry Department, University of Glasgow, Glasgow, Scotland, U.K.
Further Information

Publication History

Received: September 20, 2007 Revised: November 14, 2007

Accepted: November 23, 2007

Publication Date:
18 January 2008 (online)

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Abstract

A new rearranged nor-secoiridoid, anthocleistenolide (1), along with the known 1-hydroxy-3,7-dimethoxyxanthone (2), 1-hydroxy-3,7,8-trimethoxyxanthone (3), 7α-hydroxysitosterol (4) and sitosterol 3-O-β-D-glucopyranoside (5), were isolated from the stem bark of Anthocleista vogelii. Their structures were elucidated on the basis of spectral studies and comparison with published data. Compounds 1 - 3 and 5 were evaluated for their antibacterial and antifungal activities. Relatively low anti-staphylococcal (MIC = 200 μg/mL against Staphylococcus aureus) and anti-enterococcal (MIC = 100 μg/mL against Enterococcus faecalis) activities were observed for 1, while compounds 2 and 3 were active against Candida parapsilosis (MIC = 200 μg/mL for 2 and 25 μg/mL for 3). Compound 5 was inactive against all the bacterial and fungal species used.

References

Dr. Mathieu Tene

Department of Chemistry

University of Dschang

P. O. Box 67

Dschang

Cameroon

Phone: +237-7780-8420

Fax: +237-3345-1735

Email: mtene2001@yahoo.fr