Planta Med 2006; 72(4): 358-363
DOI: 10.1055/s-2005-916232
Original Paper
Natural Product Chemistry
© Georg Thieme Verlag KG Stuttgart · New York

New Prenylated Metabolites of Deguelia longeracemosa and Evaluation of their Antimicrobial Potential

Aderbal F. Magalhães1 , Ana Maria G. A. Tozzi2 , Eva G. Magalhães1 , Lourdes C. Souza-Neta1
  • 1Organic Chemistry Department, Chemistry Institute, UNICAMP, Campinas, São Paulo, Brazil
  • 2Botany Department, Biology Institute, UNICAMP, Campinas, São Paulo, Brazil.
Further Information

Publication History

Received: February 17, 2005

Accepted: September 21, 2005

Publication Date:
20 January 2006 (online)

Abstract

The analysis of root extracts from Deguelia longeracemosa (Benth.) A.M.G. Azevedo yielded fifteen prenylated metabolites. Nine of them are novel, and their molecular structures were determined through spectral analyses (UV, IR, MS and NMR) as being five derivatives of 4-hydroxy-3-phenylcoumarin: 4-hydroxy-3-(4′-hydroxyphenyl)-5-methoxy-6-(8′,9′-epoxy-9′-methylbutyl)-2′′,2′′-dimethylpyrano-(5′′,6′′:8,7)-coumarin; 4-hydroxy-3-(3′,4′-methylenedioxyphenyl)-5-methoxy-6-(3,3-dimethylallyl)-2′′,2′′-dimethypyrano-(5′′,6′′:8,7)-coumarin; 4-hydroxy-3-(3′-hydroxy-4′-methoxyphenyl)-5-methoxy-6-(3,3-dimethylallyl)-2′′,2′′-dimethylpyrano-(5′′,6′′:8,7)-coumarin; 4-hydroxy-3-(3′-hydroxy-4′-methoxyphenyl)-5-methoxy-2′′,2′′-dimethylpyrano-(5′′,6′′:6,7)-coumarin and 4-hydroxy-3-[4′-O-(3,3-dimethylallyl)phenyl]-5-methoxy-2′′,2′′-dimethylpyrano-(5′′,6′′:6,7)-coumarin, three derivatives of 1,2-diphenyl-1,2-ethanodione (α-oxodeoxybenzoin derivatives): 1-[6-hydroxy-2-methoxy-3-(3,3-dimethylallyl)-2′′,2′′-dimethylpyrano-(5′′,6′′:5,4)- ]-2-(4′-hydroxyphenyl)-1,2-ethanedione; 1-[6-hydroxy-2-methoxy-2′′,2′′-dimethylpyrano-(5′′,6′′:3,4)]-2-(4′-methoxyphenyl)-1,2-ethanedione; 1-[6-hydroxy-2-methoxy-2′′,2′′-dimethylpyrano-(5′′,6′′:3,4)]-2-(3′,4′-methylenedioxyphenyl)-1,2-ethanedione and one derivative of deoxybenzoin: 2,4′-dimethoxy-6-hydroxy-2′′,2′′-dimethylpyrano-(5′′,6′′:3,4)-deoxybenzoin. The antimicrobial activity of roots extracts and some isolated compounds was screened through bioautography against bacteria and fungi.

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Aderbal F. Magalhães

Departamento de Química Orgânica

IQ, UNICAMP

CP 6154

Campinas 13084-971

SP

Brazil

Phone: +55-19-3788-3064

Fax: +55-19-3788-3023

Email: aderbal@iqm.unicamp.br

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