2013
DOI: 10.1590/s1984-82502013000400017
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Phenolic compounds and antioxidant, antimicrobial and antimycobacterial activities of Serjania erecta Radlk. (Sapindaceae)

Abstract: Serjania erecta Radlk.(Sapindaceae) is a medicinal plant traditionally used in Brazil. We assayed the ethanolic extract of leaves and roots against seven microorganisms. The REMA (Resazurin Microtiter Assay) assay was used to measure the biological activity in vitro against Mycobacterium tuberculosis and our results showed moderate activity of the ethanolic extract. On the other hand S. aureus, P. aeruginosa, S. setubal, C. albicans, S. cerevisiae and E. coli revealed that the leaves and roots of S. erecta inh… Show more

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Cited by 28 publications
(15 citation statements)
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“…Only the flavonoid C-glucosides, vitexin, and isovitexin have been described previously for the Serjania genus. 4 In the work described here, cassiaoccidentalin A (2), tetrastigma B (3),…”
Section: Journal Of Natural Productsmentioning
confidence: 99%
“…Only the flavonoid C-glucosides, vitexin, and isovitexin have been described previously for the Serjania genus. 4 In the work described here, cassiaoccidentalin A (2), tetrastigma B (3),…”
Section: Journal Of Natural Productsmentioning
confidence: 99%
“…Phenolic compounds comprise a broad class of secondary metabolites that possess a large spectrum of biological properties [9][10][11][12], and they have been successfully investigated for the treatment of systemic and superficial mycoses caused by different human pathogenic fungi [13][14][15][16][17]. Benzoic and cinnamic acids and their derivatives play an important role in antifungal activity, and several studies have focused on this bioactivity [18][19][20][21][22][23][24][25].…”
Section: Introductionmentioning
confidence: 99%
“…The chemical investigation on the L. racemosa leaves collected at Kien Giang province, Viet Nam led to the isolation of ten compounds including the new one (1) by the use of efficient separation techniques ( Figure 1). The known compounds were identified as myricetin (2) [6] [10], gallic acid (8) [11], kaempferol (9) [12] and (3S,5R,6S,7E)-3,5,6trihydroxy-7-megastigmen-9-one (10) [13] via spectroscopic data analysis and comparison with those reported in the literature. In the 1 H NMR spectrum, the two anomeric proton signals at δ H 4.89 (a broad singlet, H-1) and 4.84 (a doublet, J = 1.0 Hz, H-1) showed that the two 1-OH and 1-OH groups were at the axial positions.…”
mentioning
confidence: 99%