1997
DOI: 10.1016/s0378-8741(97)00065-2
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The antimicrobial activity of 3,5,7-trihydroxyflavone isolated from the shoots of Helichrysum aureonitens

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Cited by 180 publications
(109 citation statements)
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“…The IC50 value of the acetone leaf extract (0.13, 61.7%) is significantly higher than that of standard (vitamin C 0.30, 74.3%) the result is in agreement with Omoruyi et al (2012), who reported that IC50 values of methanol plant extract is significantly higher than that of BHT and Rutin. It was also revealed that the leaf extracts contain antioxidant properties than the bark extracts as shown in Table 2; this implies that most bioactive compound are stored on the trichomes which might probably be on the leaves as reported by Afolayan and Meyer (1997). This result shed more light on the scavenging potency of C. anisata and medicinal properties of this genus in South Africa which is in agreement with the report of York et al (2012).…”
Section: Abts Radical -Scavenging Activitysupporting
confidence: 85%
“…The IC50 value of the acetone leaf extract (0.13, 61.7%) is significantly higher than that of standard (vitamin C 0.30, 74.3%) the result is in agreement with Omoruyi et al (2012), who reported that IC50 values of methanol plant extract is significantly higher than that of BHT and Rutin. It was also revealed that the leaf extracts contain antioxidant properties than the bark extracts as shown in Table 2; this implies that most bioactive compound are stored on the trichomes which might probably be on the leaves as reported by Afolayan and Meyer (1997). This result shed more light on the scavenging potency of C. anisata and medicinal properties of this genus in South Africa which is in agreement with the report of York et al (2012).…”
Section: Abts Radical -Scavenging Activitysupporting
confidence: 85%
“…Afolayan and Meyer (1997) isolated a flavone derivative, 3,5,7-trihydroxyflavone, with potent antimicrobial activity from H. aureonitens Sch. Bip.…”
Section: Discussionmentioning
confidence: 99%
“…The agar medium containing the extracts at final concentrations of 0.1, 0.5, 1.0, 2.5, and 5.0 mg=ml were poured into Petri dishes, swirled carefully until the agar began to set. Plates were left overnight for the solvents to evaporate (Afolayan & Meyer, 1997). Plates containing 5 ml of acetone or methanol were used as controls (Dulger & Ugurlu, 2005).…”
Section: Preparation Of Agar-extract Platesmentioning
confidence: 99%