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Anti-inflammatory Activities of New Succinic and Maleic Derivatives from the Fruiting Body of Antrodia camphorata

机译:樟脑樟子实体子中新的琥珀酸和马来酸衍生物的抗炎活性

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Six new compounds, trans3-isobutyl-4-[4-(3-methyl-2-butenyloxy)phenyl]pyrrolidine-2,5-dione (1), trans-1-hydroxy-3-(4-hydroxyphenyl)-4-isobutylpyrrolidine-2,5-dione(2), cis-3-(4-hydroxyphenyl)-4-isobutyldihy-drofuran-2,5-dione (3), 3-(4-hydroxyphenyl)-4-isobutyl-1 H-pyrrole-2,5-dione (4), 3-(4-hydroxyphenyl)-4-isobutylfuran-2,5-dione (5), and dimethyl 2-(4-hydroxyphenyl)-3-isobutylmaleate (6), together with one known compound, 3-isobutyl-4-[4-(3-methyl-2-butenyloxy)phenyl]furan-2,5-dione (7), were isolated from the fruiting bodies of Antrodia camphorata. The structures of the compounds were elucidated by analysis of their spectroscopic data. To investigate the immunomodulatory potential of the compounds, RAW264.7 macrophage cells were treated with the compounds. Compound 1 significantly increased spontaneous TNF-α secretion from unstimulated RAW264.7 cells but suppressed IL-6 production [50% inhibition concentration value (IC_(50)) = 10 μg/mL] in LPS-stimulated cells. Compounds 3,4, and 6 also suppressed IL-6 production with IC_(50) values of 17, 18, and 25 μg/mL, respectively, suggesting that these four compounds may have an anti-inflammatory effect on macrophage-mediated responses. Of the six compounds, compound 1 was the most effective, exerting both immunostimulatory and anti-inflammatory effects.
机译:六种新化合物,反式3-异丁基-4- [4-(4-(3-甲基-2-丁烯氧基)苯基]吡咯烷-2,5-二酮(1),反式-1-羟基-3-(4-羟基苯基)-4 -异丁基吡咯烷-2,5-二酮(2),顺式-3-(4-羟苯基)-4-异丁基二氢呋喃-2,5-二酮(3),3-(4-羟苯基)-4-异丁基-1 H-吡咯-2,5-二酮(4),3-(4-羟苯基)-4-异丁基呋喃-2,5-二酮(5)和2-(4-羟苯基)-3-异丁基马来酸二甲酯(6)从樟脑樟子实体的子实体中分离出与一种已知的化合物3-异丁基-4- [4-(4-(3-甲基-2-丁烯氧基)苯基]呋喃-2,5-二酮(7)。通过分析其光谱数据阐明了化合物的结构。为了研究这些化合物的免疫调节潜力,用该化合物处理了RAW264.7巨噬细胞。在LPS刺激的细胞中,化合物1显着增加了未刺激的RAW264.7细胞的自发TNF-α分泌,但抑制了IL-6的产生[50%抑制浓度值(IC_(50))= 10μg/ mL]。化合物3,4和6还抑制IL-6的产生,IC_(50)值分别为17、18和25μg/ mL,表明这四种化合物可能对巨噬细胞介导的反应具有抗炎作用。在这六种化合物中,化合物1最有效,同时发挥免疫刺激和抗炎作用。

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