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DOI: 10.1055/s-2002-36346
Antibacterial Activity of a Stearic Acid Derivative from Stemodia foliosa
Publication History
Received: April 8, 2002
Accepted: July 28, 2002
Publication Date:
20 December 2002 (online)
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Abstract
From the hexane-soluble fraction of an ethanol extract from leaves and stems of Stemodia foliosa (Scrophulariaceae), the new stearic acid 4-[(n-pentoxy)phenethyl] ester (1) was isolated. This compound exhibited antibacterial properties at 10 μg/mL concentration by using disc diffusion method against Gram-positive bacteria Bacillus cereus and Bacillus subtilis and fast-acid bacterium Mycobacterium fortuitum. The structure of the new compound was elucidated by spectroscopic methods and by chemical conversion.
References
- 1 Barroso G. Sistemática de Angiospermas do Brasil. Vol. 3 Viçosa; Universidade Federal de Viçosa 1991: 124-30
- 2 Chamy M C, Piovano M, Garbarino J A, Gambaro V. Stemodane diterpenoids from Stemodia chilensis . Phytochemistry. 1991; 30 1719-21
- 3 Hufford C D. H-1-NMR and C-13-NMR Assignments for the Stemodia diterpenes stemodin, stemodinone and maritimol. J Nat Prod. 1988; 51 367-9
- 4 Weniger B, Haagberrurier M, Anton R. Plants of Haiti used as antifertility agents. J Ethnopharmacol. 1982; 6 67-84
- 5 Correa M P. Dicionário das Plantas Úteis do Brasil e das Exóticas Cultivadas. Rio de Janeiro; Ministério da Agricultura, IBDF 1978: 182-97
- 6 Watt B, Collee J G. Bacterial challenges and evolving antibacterial drug strategy. Postgrad Med J. 1992; 68 6-21
- 7 National Committee for Clinical Laboratory Standards, 3rd. ed., Approved Standard M7-A3, NCCLS, Villanova, PA. 1993
- 8 Holland H L, Diakow P RP, Taylor G J. C-13 Nuclear magnetic-resonance spectra of some C-19-hydroxy, C-5,6 epoxy, C-24 ethyl, and C-19-norsteroids. Can. J. Chem.. 1978; 56 3121-7
- 9 Mahato S B, Kundu A P. C-13 NMR spectra of pentacyclic triterpenoids - A compilation and some salient features. Phytochemistry. 1994; 37 1517-75
Vanderlan da Silva Bolzani
NuBBE (Núcleo de Bioensaio, Biossíntese e Ecofisiologia de Produtos Naturais)
Instituto de Química
Universidade Estadual Paulista
CP 355, CEP 14801-970
Araraquara
SP, Brazil
Email: bolzaniv@iq.unesp.br