Planta Med 2008; 74(12): 1463-1467
DOI: 10.1055/s-2008-1081331
Natural Products Chemistry
Original Paper
© Georg Thieme Verlag KG Stuttgart · New York

Flavonoids from Pterocaulon alopecuroides with Antibacterial Activity

Rosana Alarcón1 , Roberto Carrizo Flores2 , Soledad Ocampos1 , Alejandro Lucatti1 , Laura Flores Galleguillo1 , Carlos Tonn2 , Virginia Sosa3
  • 1Facultad de Ciencias Naturales, Universidad Nacional de Salta (UNSa), Salta, Argentina
  • 2INTEQUI-CONICET – Área de Química Orgánica, Facultad de Química, Bioquímica y Farmacia. Universidad Nacional de San Luis, San Luis, Argentina
  • 3Departamento de Química Orgánica, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba, Instituto Multidisciplinario de Biología Vegetal – IMBIV (CONICET-UNC), Córdoba, Argentina
Further Information

Publication History

Received: February 28, 2008 Revised: May 30, 2008

Accepted: June 18, 2008

Publication Date:
14 August 2008 (online)

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Abstract

Three flavonoids, (2R,3R)-5,4′-dihydroxy-3′-O-methyl-7-(γ,γ-dimethylallyloxy)dihydroflavonol 1, (2R,3R)-5,7,4′-trihydroxy-3′-O-methyl-6-(α,α-dimethylallyl)dihydroflavonol 2, and (2R,3R)-5,7,4′-trihydroxy-6-(α,α-dimethylallyl)dihydroflavonol 3, together with three known flavonoids (4 – 6), were isolated from the aerial parts of Pterocaulon alopecuroides. The structures of the compounds were determined by mass and by 1 D and 2 D NMR spectroscopy. Screening of the antibacterial activity of all six compounds was conducted by a disc diffusion test against Bacillus cereus, Bacillus subtilis, Salmonella typhimurium and Proteus mirabilis. The minimum inhibitory concentration (MIC) of the active compounds (2, 3, 4, 6) was determined by a microdilution assay. These compounds were active only against both Gram (+) bacteria with MIC values ≤ 200 μg/mL.

References

Dr. Rosana Alarcón

Facultad de Ciencias Naturales

Universidad Nacional de Salta

Av. Bolivia 5150

4400 Salta

Argentina

Phone: +54-387-425-5491

Fax: +54-387-425-5455

Email: ralarcon@unsa.edu.ar