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Structures and Inhibitory Activities for Interleukin-2 Production of Seasonally Variable Constituents in Flower Parts of Magnolia kobus at Different Growth Stages

机译:在不同生长阶段的玉兰科斯花型季节性可变成分的白细胞介素-2生产的结构和抑制作用

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Magnolia Flower is a crude drug used for the treatment of headaches, toothaches, and nasal congestion. Here, we focused on Magnolia kobus , one of the botanical origins of Magnolia Flower, and collected the flower parts at different growth stages to compare chemical compositions and investigate potential inhibitory activities against interleukin-2 (IL-2) production in murine splenic T cells. After determining the structures, we examined the inhibitory effects of the constituents of the bud, the medicinal part of the crude drug, against IL-2 production. We first extracted the flower parts of M. kobus from the bud to fallen bloom stages and analysed the chemical compositions to identify the constituents characteristic to the buds. We found that the inhibitory activity of the buds against IL-2 production was more potent than that of the blooms. We isolated two known compounds, tiliroside ( 1 ) and syringin ( 2 ), characteristic to the buds from the methanol (MeOH) extract of Magnolia Flower. Moreover, we examined the inhibitory activities of both compounds against IL-2 production and found that tiliroside ( 1 ) but not syringin ( 2 ), showed strong inhibitory activity against IL-2 production and inhibited its mRNA expression. Thus, our strategy to examine the relationship between chemical compositions and biological activities during plant maturation could not only contribute to the scientific evaluation of medicinal parts of crude drugs but also assist in identifying biologically active constituents that have not yet been reported.
机译:玉兰花是一种用于治疗头痛,牙痛和鼻塞的粗药物。在这里,我们专注于玉兰玉兰花的植物起源之一,并在不同的生长阶段收集了花零件,以比较化学成分,并调查鼠脾脏T细胞中的白细胞介素-2(IL-2)产生的潜在抑制活动。在确定结构后,我们检查了芽,粗药物的药物部分的抑制作用对抗IL-2产生。我们首先从芽中提取了芽孢杆菌的花部位,以落入盛开的阶段,并分析化学组合物以鉴定对芽的成分特征。我们发现对IL-2产生的芽的抑制活性比盛开的含量更有效。我们孤立两种已知的化合物,噻罗膦(1)和切割蛋白(2),其特征从甲醇(MeOH)提取物的芽的芽。此外,我们研究了两种化合物对IL-2产生的抑制作用,发现硫罗膦酰基(1)但不是切割蛋白(2),表明对IL-2产生的强烈抑制活性并抑制其mRNA表达。因此,我们对植物成熟期间化学成分和生物活性之间的关系的策略不仅有助于对粗药物的药物部位的科学评估,而且还有助于鉴定尚未报告的生物学活性成分。

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