2003
DOI: 10.1016/j.phytochem.2003.08.002
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Immunosuppressive flavones and lignans from Bupleurum scorzonerifolium

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Cited by 40 publications
(26 citation statements)
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“…The acetone extract AE-BS was prepared as described previously [25,32] . The AE-BS was dissolved in 95% MeOH solution and then partitioned (1:1) with n-hexane to give the n-hexane-soluble fraction (BS-HE).…”
Section: Methodsmentioning
confidence: 99%
“…The acetone extract AE-BS was prepared as described previously [25,32] . The AE-BS was dissolved in 95% MeOH solution and then partitioned (1:1) with n-hexane to give the n-hexane-soluble fraction (BS-HE).…”
Section: Methodsmentioning
confidence: 99%
“…The isolated compounds wogonin, eugenin and saikochromone A inhibited the secretion at a dose of 10 mg/ml by 99, 72 and 71%, respectively. [50] The acidic polysaccharide fraction from B. smithii inhibited the complement activation (IC50 340 and 81 mg/ml) for both classical and alternative pathways, respectively. This inhibition was mediated through interaction with C1s, C3 and C4 complements, which are the major components of the innate immune system.…”
Section: Immunomodulatory Activitymentioning
confidence: 96%
“…[102] Buddlejasaponin I, IV and the sulfated saikosaponin (sandrosaponin I), which were isolated from B. rigidum, exhibited a very potent in-vivo anti-inflammatory effect (1 mg/ear dose) on mouse ear oedema induced by PMA compared with the equivalent dose of indometacin. The effect of these compounds on other inflammatory parameters [109] Rotundioside F (-) Acute inflammation [109] Rotundioside A, H, I, J Cytotoxic against MK-1, HeLa and B16F10 cell lines [30,110] B. salicifolium Polyacetylenes derivatives Antibacterial [111,112] B. scorzonerifolium Acetone extract Cytotoxic against A549 cell line [113][114][115] Wogonin, eugenin, saikochromone A (-) IL-2 [50] Saikosaponin B3, bupleurosides III, VI, IX and XIII and scorzonerosides A, B, C…”
Section: B Rigidummentioning
confidence: 99%
“…17) Therefore, the absolute configuration of C-3 of compound 1 opposite that of isochaihulactone and should be 3S. Consequently, the structure of compound 1 was elucidated as (3S,6Z)-2-(3Ј,4Ј,5Ј-trimethoxybenzylidene)-3-(3Љ,4Љ-methylenedioxybenzyl)-g-butyrolactone.…”
Section: Resultsmentioning
confidence: 99%