1973
DOI: 10.1007/bf01032018
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The structure of calenduloside A

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Cited by 5 publications
(3 citation statements)
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“…The therapeutic effects of the C. officinalis is caused by a significant group of secondary metabolites called terpenoids. 1,8,41 Various terpenoids isolated (Figure 2) are calenduladiol-3-O-palmitate, stigmasterol, lupeol, Ψ-taraxasteol, 42 8,43 calendulosides A-H, 8,37,44 and calendulaglycoside A and B. 27,45…”
Section: Terpenoidsmentioning
confidence: 99%
“…The therapeutic effects of the C. officinalis is caused by a significant group of secondary metabolites called terpenoids. 1,8,41 Various terpenoids isolated (Figure 2) are calenduladiol-3-O-palmitate, stigmasterol, lupeol, Ψ-taraxasteol, 42 8,43 calendulosides A-H, 8,37,44 and calendulaglycoside A and B. 27,45…”
Section: Terpenoidsmentioning
confidence: 99%
“…In addition to oleanolic acid, β-sitosterol and salvigenin, which have been previously isolated from the plant [9c], the triterpenoids 3-formyl-ursolic acid, 20 2α,3β,23-trihydroxyurs-12-en-28-oic acid (asiatic acid), 21 3- O -β-galactopyranosyloleanolic acid, 22 betulinic acid, 23 the steroidal compound daucosterol, 24 the flavonoid apigenin-7- O -glucoside, 25 the phenyl ethanoid 2-(4-hydroxyphenethyl) tetratriacontanoate, 26 and the phenolic compound rosmarinic acid 27 were isolated and are described here from S. hydrangea for the first time.…”
mentioning
confidence: 99%
“…The remaining three saponins (D2, C, and A) were the 28^-D-glucopyranosyl ester of glycosides F, D, and B, respectively. However, among these proposed structures, only those of glycosides F and D2 were clearly established by comparison with calenduloside F (6).…”
mentioning
confidence: 99%