2015
DOI: 10.1016/j.phytochem.2014.12.026
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Carnosic acid

Abstract: Carnosic acid (salvin), which possesses antioxidative and antimicrobial properties, is increasingly exploited within the food, nutritional health and cosmetics industries. Since its first extraction from a Salvia species (∼70 years ago) and its identification (∼50 years ago), numerous articles and patents (∼400) have been published on specific food and medicinal applications of Rosmarinus and Salvia plant extracts abundant in carnosic acid. In contrast, relevant biochemical, physiological or molecular studies … Show more

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Cited by 261 publications
(243 citation statements)
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“…The main diterpenes isolated from S. pomifera leaves include salviol (6), pisiferic acid (7), carnosol (8), 12-methoxy-carnosic acid (9), O-methyl-pisiferic acid (10), and 2α-hydroxy-O-methyl-pisiferic acid (11) (Bottom). (B) The biosynthesis of tanshinone and carnosic acid begins with the cyclization of GGPP (12) by a class II diTPS to produce (+) copalyl diphosphate (CPP) (13), which is in turn converted to miltiradiene (14) by a class I diTPS. Spontaneous oxidation of 14 gives rise to abietatriene (15), which is oxidized to ferruginol (16) by a CYP enzyme.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…The main diterpenes isolated from S. pomifera leaves include salviol (6), pisiferic acid (7), carnosol (8), 12-methoxy-carnosic acid (9), O-methyl-pisiferic acid (10), and 2α-hydroxy-O-methyl-pisiferic acid (11) (Bottom). (B) The biosynthesis of tanshinone and carnosic acid begins with the cyclization of GGPP (12) by a class II diTPS to produce (+) copalyl diphosphate (CPP) (13), which is in turn converted to miltiradiene (14) by a class I diTPS. Spontaneous oxidation of 14 gives rise to abietatriene (15), which is oxidized to ferruginol (16) by a CYP enzyme.…”
Section: Resultsmentioning
confidence: 99%
“…S3A, b, S19, and S20). The remaining compound in this group could result from oxidative degradation and rearrangement of carnosic acid to a molecule bearing a catechol, quinone, or semiquinone feature at C-12-C-11 (13,43,44), but insufficient amounts precluded characterization at this stage. The last group of compounds displayed 343 m/z as the most abundant fragment ion (SI Appendix, Fig.…”
Section: Resultsmentioning
confidence: 99%
“…However, 90% of the antioxidant properties of RE were reported to be from their carnosic acid and carnosol constituents (Aruoma et al, 1992;Erkan et al, 2008). The mechanism of this antioxidant activity is related to its phenolic diterpene structure which works as hydrogen donor and scavenging free radical compounds (Houlihan et al, 1984;Schwarz & Ternes, 1992;Hall et al, 1998;Richhelmer et al, 1999;Birtic et al, 2015).…”
Section: Introductionmentioning
confidence: 99%
“…It was recently shown that diet enriched with Se-compounds and CA (both with antioxidative properties) modifies ruminal microbiota and hence FAs metabolism in the rumen (Morán et al, 2013;Birtić et al, 2015). As a consequence, the addition of dietary Se-compounds and/or CA affects FAs profile and levels of amino acids in the rumen and has a significant influence on biosynthesis of volatile compounds and concentrations of FAs, cholesterol and amino acids in lamb tissues (Miltko et al, 2016;Rozbicka-Wieczorek et al, 2016a,b,c).…”
Section: Introductionmentioning
confidence: 99%