1983
DOI: 10.1016/s0031-9422(00)80267-8
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Eudesmane derivatives from pluchea odorata

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Cited by 35 publications
(17 citation statements)
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“…It was shown that it contains flavonoids, triterpenes (28,29), phytosterols (44), and Plucheinol, an eudesmane type sesquiterpene unique to P. odorata (30,31). A comparison between two P. odorata populations from Mexico and El Salvador showed that the Mexican population contained a greater number of triterpenes and flavonoids, whereas the plants from El Salvador contained a greater number of sesquiterpenes (29,45). Whether the different P. odorata populations also exhibit different anti-cancer activity needs to be established and could elucidate which type(s) of the plant constituents may be responsible for the here described effects.…”
Section: Discussionmentioning
confidence: 99%
“…It was shown that it contains flavonoids, triterpenes (28,29), phytosterols (44), and Plucheinol, an eudesmane type sesquiterpene unique to P. odorata (30,31). A comparison between two P. odorata populations from Mexico and El Salvador showed that the Mexican population contained a greater number of triterpenes and flavonoids, whereas the plants from El Salvador contained a greater number of sesquiterpenes (29,45). Whether the different P. odorata populations also exhibit different anti-cancer activity needs to be established and could elucidate which type(s) of the plant constituents may be responsible for the here described effects.…”
Section: Discussionmentioning
confidence: 99%
“…(200 ≤ MIC 100 ≤ 400 mg/ml), and the hexanic extract of P. carolinensis showed a low anti-Pneumocystis activity (MIC 100 = 100 mg/ml). The identification of some sesquiterpenes (eudesmane and cuathemone structure), phenolic compounds (flavonols, phenolic acids) and triterpenes has been reported (Ahmed et al, 1998;Arriaga and Borges-Del-Castillo, 1983;Arriaga and Borges-Del-Castillo, 1985;Dominguez and Zamudio, 1972;Gupta, 1995;Perera et al, 2007 ;Perera Córdova et al, 2010;Wollenweber et al, 1985).…”
Section: Resultsmentioning
confidence: 99%
“…The CH 2 Cl 2 extract exhibited antimalarial activity (IC 50 = 3.6 g/ml), which was considered promissory according present endpoint criteria for medicinal plants extracts (Huber and Koella, 1993;Soh and Benoit-Vical, 2007). After several separation steps, the most bioactive fractions were deeper studied until yielding seven pure metabolites which were identified as eudesmin (1) (Latip et al, 1999), magnolin (2) (Seo, 2010), epimagnolin A (3) (Seo, 2010), aschantin (4) (Ahmed et al, 2002), kobusin (5) (Latip et al, 1999), sesamin (6) (Kuropka and Glombitza, 1987) and artemetin (7) (Arriaga-Giner et al, 1983), respectively based on spectroscopic analyses and comparison with reported NMR data (Fig. 1).…”
Section: Resultsmentioning
confidence: 99%