1999
DOI: 10.1016/s0031-9422(98)00718-3
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Sesquiterpene lactone glycosides from Lapsana communis L. subsp. communis.

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Cited by 13 publications
(5 citation statements)
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“…Seco-tanapartholide C is classified in guaiane-type sesquiterpene lactones (SQLs), which are also abundantly present in Compositae (Heinrich et al, 1998). Guaiane-type SQLs have also been found in the glucoside form (Fontanel et al, 1999). Therefore, seco-tanapartholide C may be generated by catalytic activity of β-glucosidase in the fermentation process using the SN13T strain.…”
Section: Discussionmentioning
confidence: 99%
“…Seco-tanapartholide C is classified in guaiane-type sesquiterpene lactones (SQLs), which are also abundantly present in Compositae (Heinrich et al, 1998). Guaiane-type SQLs have also been found in the glucoside form (Fontanel et al, 1999). Therefore, seco-tanapartholide C may be generated by catalytic activity of β-glucosidase in the fermentation process using the SN13T strain.…”
Section: Discussionmentioning
confidence: 99%
“…1. The other purified components (4-12) were identified as ixerin N (4) [7], ixerisoside A (5) [8], ixerin M (6) [7], tectroside (7) [8,13], 8-epidesacylcynaropicrin glucoside (8) [7,14], 8-epiisolipidiol (9, 3β,8β-dihydroxy-guaia-10(14)-en-1α,4β,5α,6β,7α,11βH-12,6αolide) [11,12], 11βH-11,13-dihydrointegrifolin (10, 3β,8β-dihydroxy-guaia-4(15),10(14)-dien-1α,5α,6β,7α, 11βH-12,6α-olide) [15,16], 8β-hydroxy-4β,15-dihydrozaluzanin C (11, 3β,8β-dihydroxy-guaia-10(14),11(13)-dien-1α,4β,5α,6β,7αH-12,6α-olide) [11] and integrifolin (12, 3β,8β-dihydroxy-guaia-4(15),10(14),11 (13)-trien-1α,5α,6β,7αH-12,6α-olide) [17] by direct comparison of their spectral data with those in the literature. Details of the workup procedure and copies of the original spectra of 4-12 are obtainable from the author of correspondence.…”
mentioning
confidence: 99%
“…The cytotoxic effect of crepiside E was also investigated by other authors on SK‐MEL‐2 (human melanoma), SK‐OV‐3 (human ovary adenocarcinoma), HCT15 (human colorectal adenocarcinoma) and A549 cells (concentrations up to 12.7 μg/mL), [47] as well as on L1210 (mouse lymphocytic leukemia) cells (concentrations up to 5.0 μg/mL), [48] but in tested concentrations the compound did not achieve 50 % inhibition of the growth of these cells. On the other hand, desacylcynaropicrin, which is the crepiside E aglycone, was shown to be a potent cytotoxic agent for HeLa ( IC 50 =1.4 μg/mL), [49] SK‐MEL‐2 ( IC 50 =3.6 μg/mL), XF498 (human glioblastoma, IC 50 =3.9 μg/mL), HCT15 ( IC 50 =6.0 μg/mL), SK‐OV‐3 ( IC 50 =11.9 μg/mL) and A549 cells ( IC 50 =13.3 μg/mL) [50] .…”
Section: Resultsmentioning
confidence: 99%