2000
DOI: 10.1016/s0367-326x(00)00202-1
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Lantana camara L. (Verbenaceae)

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Cited by 354 publications
(293 citation statements)
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References 77 publications
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“…The aforementioned data were coherent with a non aromatic abietane-type diterpene that displays an epoxy ring, a tertiary hydroxyl group, an α,β-unsaturated-γ-lactone system and two double bonds, having some similarities with the diterpene triptolide. 12 The location of these functions in the abietane skeleton was deduced through additional HMBC analysis (Table 1), which revealed the following long-range correlations: the epoxy hydrogens at d is generally present in abietane-type diterpenoids. 13 Finally, the butenolide ring involving the carbons C-3, C-4, C-18 and C-19 was located by the correlations of the methylene hydrogens at d 67 (H-6α) and 1.07 (H-7α).…”
Section: Resultsmentioning
confidence: 99%
“…The aforementioned data were coherent with a non aromatic abietane-type diterpene that displays an epoxy ring, a tertiary hydroxyl group, an α,β-unsaturated-γ-lactone system and two double bonds, having some similarities with the diterpene triptolide. 12 The location of these functions in the abietane skeleton was deduced through additional HMBC analysis (Table 1), which revealed the following long-range correlations: the epoxy hydrogens at d is generally present in abietane-type diterpenoids. 13 Finally, the butenolide ring involving the carbons C-3, C-4, C-18 and C-19 was located by the correlations of the methylene hydrogens at d 67 (H-6α) and 1.07 (H-7α).…”
Section: Resultsmentioning
confidence: 99%
“…Its toxicity was also showed in ruminant grazing animals (Tokarnia et al, 1999). On the other hand, therapeutics characteristics of this plant should be considered once the population uses it to treat several health disorders as respiratory diseases, rheumatisms, malaria, dysenteries, headache, hypertension and cancer (Ghisalberti, 2000;Deena & Thoppil, 2000). The literature has shown that the essential oil from leaves of L. camara (EOLC) was able to play as an anti-inflammatory agent in vivo and has a potential antimicrobial action in vitro (Deena & Thoppil, 2000).…”
Section: Introductionmentioning
confidence: 99%
“…Kauranes are intermediates in the biosynthesis of a number of plant and fungal metabolites, including the gibberellins and other phytohormones involved in the regulation of growth and development of higher plants. 6 Kaurenoic acid (1), along with several related kauranes, 7 exhibits a wide variety of biological activities such as antimicrobial, anti-inflammatory, anti-fertility, cytotoxic, and trypanocidal. [8][9][10][11][12][13][14][15][16] The relatively high natural abundance of kaurenoic acid (1) and the inexistence of a general method for the synthesis of alkyl kaurenoates by esterification of 1 provides further motivation to investigate its chemical modification 17 in order to obtain derivatives and test their pharmacological activity.…”
Section: Introductionmentioning
confidence: 99%