Sesquiterpene lactones of Eupatorium cannabinum

Kotov, A. G.; Darmograi, R. E.; Rosik, G. G.; Komissarenko, N. F.; Ladnaya, L. Ya.

doi:10.1007/bf00597871

Cited by 3 publications

(2 citation statements)

References 2 publications

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“…These lactones were generally most active against Chycobacterium tuberculosis. "' The following sesquiterpene lactones 53,154 ## Pharmacological studies of the sesquiterpene lactones confirmed the antitumor activity of eupatoriopicrin.…”

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confidence: 81%

Sesquiterpene lactones from the Yugoslavian wild growing plant families asteraceae and apiaceae

Milosavljević

Bulatovic

Stefanović

1999

JSCS

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1. Introduction 2. Results 3. Asteraceae 3.1. Genus Artemisia L. 3.1.1. Artemisia annua L. 3.1.2. Artemisia vulgaris L. 3.1.3. Artemisia absinthium L. (warmwood) 3.1.4. Artemisia scoparia W. et K. 3.1.5. Artemisia camprestris L. 3.2. Genus Ambrosia L. 3.2.1. Ambrosia artemisiifolia L. (the common rag weed) 3.3. Genus Tanacetum L. ( syn. Chrysanthemum L.) 3.3.1. Tanacetum parthenium L. (feverfew) 3.3.2. Tanacetum serotinum L. 3.3.3. Tanacetum vulgare L. (tansy) 3.3.4. Tanacetum macrophyllum Willd. 3.3.5. Tanacetum corymbosum L. 3.4. Genus Telekia Baumg. 3.4.1. Telekia speciosa (Schreb.) Baumg. 3.5. Genus Inula L. 3.5.1. Inula helenium L. 3.5.2. Inula spiraeifolia L. 3.6. Genus Eupatorium L. 3.6.1. Eupatorium cannabinum L. 3.7. Genus Achillea L. 3.7.1. Achillea abrotanoides Vis. 3.7.2. Achillea millefolium subsp. pannonica 3.7.3. Achillea crithmifolia W. et K. 3.7.4. Achillea clypeolata Sibth. et Sm. 3.7.5. Achillea serbica Nyman 3.7.6. Achillea depressa Janka 3.8. Genus Anthemis L. 3.8.1. Anthemis carpatica Willd. 3.8.2. Anthemis cretica L. subsp. cretica 3.9. Genus Centaurea L. 3.9.1. Centaurea derventana Vis. et Pan~. 3.9.2. Centaurea kosaninii Hayek 3.9.3. Centaurea solstitialis L. 4. Apiaceae 4.1. Genus Laserpitium L. 4.1.1. Laserpitium siler L. 4.1.2. Laserpitium marginatum L. 4.1.3. Laserpitium latifolium L. 4.1.4. Laserpitium alpinum W. K. 4.2. Genus Angelica L. 4.2.1. Angelica silvestris L. 4.3. Genus Peucedanum L. 4.3.1. Peucedanum austriacum (Jacq.) Koch

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confidence: 81%

Sesquiterpene lactones from the Yugoslavian wild growing plant families asteraceae and apiaceae

Milosavljević

Bulatovic

Stefanović

1999

JSCS

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“…Chen et al reported eudesmane sesquiterpenes and menthane monoterpenes as chemotaxonomic important compounds for E. fortunei [7]. However, eudesmanes were also isolated from some Eupatorium species such as E. quadrangulare [28] and E. cannabium [29]. Thymol derivatives predominantly occur in E. fortunei, some of which may be considered as species-specific substances for the identification of E. fortunei among Eupatorium species judging from their plant-dependent characteristic oxygenated patterns.…”

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confidence: 99%

Thymol Derivatives from Eupatorium fortunei

Giang¹,

Trang²,

Huong³

et al. 2019

Rec.Nat.Prod.

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The presence of thymol derivatives in the leaves and twigs of E. fortunei collected in Northern Vietnam was investigated. Five thymol derivatives, including new 9-O-angeloxy-10-hydroxy-8-methoxythymol, 10-acetoxy-9-chloro-8,9-dehydrothymol, 9-acetoxy-8,10-epoxythymol-3-O-isobutyrate, 8,10-epoxy-9-hydroxythymol-3-O-tiglate, and 9-acetoxy-8,10-epoxythymol-3-O-angelate together with six other compounds, including taraxasteryl acetate, o-coumaric acid, trans-melilotoside, (-)-loliolide, coumarin, and -sitosterol were isolated.The structures of the isolated compounds were determined on the basis of MS and NMR spectroscopic data.

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Study on the metabolites of isoalantolactone in vivo and in vitro by ultra performance liquid chromatography combined with Triple TOF mass spectrometry

Yao

Huo

et al. 2017

Food Chemistry

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Sesquiterpene lactones of Eupatorium cannabinum

Cited by 3 publications

References 2 publications

Sesquiterpene lactones from the Yugoslavian wild growing plant families asteraceae and apiaceae

Sesquiterpene lactones from the Yugoslavian wild growing plant families asteraceae and apiaceae

Thymol Derivatives from Eupatorium fortunei

Study on the metabolites of isoalantolactone in vivo and in vitro by ultra performance liquid chromatography combined with Triple TOF mass spectrometry

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