2016
DOI: 10.1016/j.bjp.2015.08.008
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Chemical composition of essential oils of leaves, flowers and fruits of Hortia oreadica

Abstract: BJP 183 1-6 Revista Brasileira de Farmacognosia xxx (2015) xxx-xxx w w w . s b f g n o s i a . o r g . b r / r e v i s t a a b s t r a c t Hortia oreadica Groppo, Kallunki & Pirani, Rutaceae, known as "para-tudo", "quina", and "quina-docampo", is used in traditional medicine locally to treat stomach pain and fevers. The aims of this study were: analyze the chemical composition of essential oils from leaves, flowers and fruits of H. oreadica and verify the seasonal variation of the chemical components of essent… Show more

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Cited by 18 publications
(10 citation statements)
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“…Santos et al. (2016) reported that the amounts of pogostol and α-yalangene in Hortia oreadica were dependent on weather conditions. Ozer et al.…”
Section: Resultsmentioning
confidence: 99%
“…Santos et al. (2016) reported that the amounts of pogostol and α-yalangene in Hortia oreadica were dependent on weather conditions. Ozer et al.…”
Section: Resultsmentioning
confidence: 99%
“…β-caryophyllene was also identified as a major component in EOs from Galeopsis bifida (22%), Vernonia remotiflora (42.2%), Vernonia brasiliana (36.7%) and Annona foetida (14.19%) (Olennikov et al, 2010;Maia et al, 2010;Costa et al, 2009). In addition, bicyclogermacrene has already been identified as a major constituent in EOs from Hortia oreadica flowers (23.28%), fruits (20.64%) and leaves (from14.71% to 31.37%) (Santos et al, 2016). In vitro antibacterial activity of EOs from S. odoratissima against the microorganisms under study and their potential activities were assessed quantitatively by minimum inhibitory concentration (MIC) values.…”
Section: Resultsmentioning
confidence: 99%
“… 37 In 2006, pogostol was confirmed in P cablin and it was proposed that the compound was produced via deprotonation of the germacradienyl cation to germacrene A, followed by deprotonation‐induced cyclization 38 . More recently, pogostol was also identified in essential oils from V zizanoides , Biscogniauxia nummularia , Valeriana jatamansi Jones and Hortia oreadica 31,39‐41 . The structural conformation of pogostol was once again contested as a result of the inconsistencies between the NMR spectroscopic data from the synthetic and naturally occurring compound isolated from B nummularia (Figure 3D).…”
Section: Resultsmentioning
confidence: 99%
“…Valeriana jatamansi Jones and Hortia oreadica. 31,[39][40][41] The structural conformation of pogostol was once again contested as a result of the inconsistencies between the NMR spectroscopic data from the synthetic and naturally occurring compound isolated from B nummularia ( Figure 3D). 39 However, the absolute configuration of pogostol was most recently confirmed using a compound with known stereochemistry, α-bulnesene and its conversion products ( Figure 3E).…”
Section: Aroma Extract Dilution Analysis and Compound Identificationmentioning
confidence: 99%