1971
DOI: 10.1039/c29710001117
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The meliacins (limonoids). Biosynthesis of nimbolide in the leaves of Azadirachta indica

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Cited by 29 publications
(19 citation statements)
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“…Apparently, the tirucallane system does not get directly transformed to limonoids. In fact, the biosynthetic studies of the limonoid nimbolide (Ekong et al, 1971;Ekong and Ibiyemi, 1985) had shown that euphol and apo-euphol rather than the tirucallol systems are the preferred intermediates in the biosynthesis of the limonoid. This hypothesis could explain the isolation of the tirucallane and not the euphane system which is biogenetically transformed to limonoids while the tirucallane system does not usually get transformed to limonoids.…”
Section: Resultsmentioning
confidence: 97%
“…Apparently, the tirucallane system does not get directly transformed to limonoids. In fact, the biosynthetic studies of the limonoid nimbolide (Ekong et al, 1971;Ekong and Ibiyemi, 1985) had shown that euphol and apo-euphol rather than the tirucallol systems are the preferred intermediates in the biosynthesis of the limonoid. This hypothesis could explain the isolation of the tirucallane and not the euphane system which is biogenetically transformed to limonoids while the tirucallane system does not usually get transformed to limonoids.…”
Section: Resultsmentioning
confidence: 97%
“…The antimalarial activity of the plant has been attributed to the presence of β-sitosterol (Basak and Chakraborty, 1968); nimbolide (Ekong et al, 1971); gedunin and other limonoids (Khalid et al, 1989).…”
Section: Discussionmentioning
confidence: 99%
“…A number of workers have shown that this plant is useful in the management of malaria therapy (Ekanem, 1978). Several active components have been isolated from the extracts of this plant so it implies that not only one of these compounds is responsible for the antimalarial activity of the plant (Basak and Chakraborty, 1968;Ekong et al, 1971;Khalid et al, 1989).…”
Section: Introductionmentioning
confidence: 99%
“…Im Petrolather-Extrakt der Wurzel indischer Herkunft wurden die unverseifbaren Anteile mit Girard-T-Reagenz [18] in eine Keton-und eine Restfraktion aufgetrennt. Die Keton-Fraktion zeigte im D C drei Flecken, von denen sich zwei als 24-Methylencycloartanon und Cycloeucalenon erwiesen, die auch im Stammholz [15,17] vorkornmen. Fur den dritten Fleck ergab sich aus den spektroskopischen Daten der Hinweis, dai3 es sich um das schwer trennbare Gemisch aus Stigmast-4-en-3-on und Campest-4-en-3-on handelt, das auch aus der Stammrinde [12]…”
Section: Ergebnisseunclassified