Three new and five known sesquiterpene lactones were isolated from the roots of Laser trilobum (L.) Borkh. Chemical identity of the known compounds and structural analysis of the new ones were determined by HR MS and NMR spectroscopy. The two new sesquiterpene lactones: 2-acetoxytrilobolide and 2-hydroxy-10-deacetyltrilobolide belong to the guaianolide type, and the third one, eudeslaserolide, to the biogenetically related eudesmanolide type. Both types, together with their biogenetic precursor of germacranolide type (laserolide) are present in L. trilobum, as well as in the related Laserpitium species. Purposefully selected set of these native sesquiterpene lactones was tested for specific immunobiological properties. The obtained results demonstrate that trilobolide and its acetoxy analog are strong activators of cytokine secretion. On the contrary, the other L. trilobum and Laserpitium siler constituents are only very mild activators, or even inhibitors of the cytokine and nitric oxide production.
Resveratrol and closely related stilbenoids belong to the most intensively studied biologically active compounds. This interest evoked several attempts to prepare such compounds in a convenient synthetic way. Our approach allowed obtaining largely methoxystilbenes, formed as E-isomers only (using Wittig–Horner synthesis as the key step), which were further demethylated by boron tribromide. The hydroxymethoxystilbenes (e.g. pterostilbene) were prepared using isopropyl protection, later selectively deprotected by boron trichloride. The method is suitable for preparing such compounds in a large amount. Effects of the obtained stilbene derivatives on immunobiological responses triggered by lipopolysacharide and interferon-γ were tested under in vitro conditions. Namely production of nitric oxide (NO) was investigated, and relation between the molecular structure and immunobiological activity was assessed.
Two lignan glucosides, the known tracheloside and the new carthamoside, together with their two known aglycones, trachelogenin and (7E,8'S)-7,8-didehydroarctigenin (cf. cartha- mogenin), were isolated from the seeds of Leuzea carthamoides. Additional four phenylpropanoid derivatives of tryptamine, the E and Z isomers of N-feruloylserotonin and N-isoferuloylserotonin, were also isolated and identified. Their structure determination and identification were performed by spectroscopic, mainly NMR analysis.
Fourteen minor ecdysteroid components were isolated and identified from the roots of Leuzea carthamoides (Willd.) DC. Two of them are new phytoecdysteroids: leuzeasterone (1) a six-member side-chain lactone, and (24Z)-29-hydroxy-24(28)-dehydromakisterone C (4) a structurally related sitostane type analogue and assumed biogenetic precursor of 1. The next one, 5α-20-hydroxyecdysone (6), is a rare A/B-ring trans-annelated epimer of the most common phytoecdysteroid 20-hydroxyecdysone. Further compounds: makisterone C (3), 3-epi-20-hydroxyecdysone (5), integristerone A (7), integristerone B (8), 22-oxo-20-hydroxyecdysone (10), taxisterone (11), rubrosterone (12), dihydrorubrosterone (13) and poststerone (14), are new constituents of L. carthamoides, though already reported as compounds isolated from other natural sources. Two earlier reported minor Leuzea ecdysteroids: the five-membered side-chain lactone carthamosterone (2) and the 11-hydroxy-substituted analogue isovitexirone (9), are also included because they are now better characterised. Certain previously described Leuzea ecdysteroids were not found in our material, which may indicate geographic, seasonal or cultivar variations.The abundant occurrence of ecdysteroids in Leuzea carthamoides DC. (syn. Rhaponticum carthamoides (Willd.) Iljin) is interesting from several viewpoints. First is the large structure variability of all so far isolated ecdysone analogues 2-8 and second is their high content in the roots or seeds of this plant 9 . L. carthamoides is endemic in Siberia, but is also cultivated as a medicinal plant on a large scale in Europe. This is why L. carthamoides can serve as a rich source of ecdysteroids, insect moulting hormone analogues,
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