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首页> 外文期刊>BMC Complementary and Alternative Medicine >Xanthine oxidase inhibitory activity of a new isocoumarin obtained from Marantodes pumilum var. pumila leaves
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Xanthine oxidase inhibitory activity of a new isocoumarin obtained from Marantodes pumilum var. pumila leaves

机译:从Marantodes浮氏素瓦朗获得的新异种Marin的黄嘌呤氧化酶抑制活性。小花叶叶子

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In traditional Malay medicine, Marantodes pumilum (Blume) Kuntze (family Primulaceae) is commonly used by women to treat parturition, flatulence, dysentery, dysmenorrhea, gonorrhea, and bone diseases. Preliminary screening of some Primulaceae species showed that they possess xanthine oxidase inhibitory activity. Thus, this study aimed to investigate the xanthine oxidase inhibitory activity of three varieties of M. pumilum and their phytochemical compounds. Dichloromethane, methanol, and water extracts of the leaves and roots of M. pumilum var. alata, M. pumilum var. pumila, and M. pumilum var. lanceolata were tested using an in vitro xanthine oxidase inhibitory assay. Bioassay-guided fractionation and isolation were carried out on the most active extract using chromatographic techniques. The structures of the isolated compounds were determined using spectroscopic techniques. The most active dichloromethane extract of M. pumilum var. pumila leaves (IC50?=?161.6?μg/mL) yielded one new compound, 3,7-dihydroxy-5-methoxy-4,8-dimethyl-isocoumarin (1), and five known compounds, viz. ardisiaquinone A (2), maesanin (3), stigmasterol (4), tetracosane (5), and margaric acid (6). The new compound was found to be the most active xanthine oxidase inhibitor with an IC50 value of 0.66?±?0.01?μg/mL, which was not significantly different (p??0.05) from that of the positive control, allopurinol (IC50?=?0.24?±?0.00?μg/mL). This study suggests that the new compound 3,7-dihydroxy-5-methoxy-4,8-dimethyl-isocoumarin (1), which was isolated from the dichloromethane extract of M. pumilum var. pumila leaves, could be a potential xanthine oxidase inhibitor.
机译:在传统的马来医学中,Marantodes Pumilum(Blume)Kuntze(家庭原始瓜素)通常被妇女用于治疗分娩,胀气,痢疾,痛经,淋病和骨病。一些血管基图像的初步筛选表明它们具有黄嘌呤氧化酶抑制活性。因此,该研究旨在研究三种M.Pumilum的黄嘌呤氧化酶抑制活性及其植物化学化合物。二氯甲烷,甲醇和叶片的水提取物和M.Pumilum var的根。 alata,m.pumilum var。 pumila和m.pumilum var。使用体外黄嘌呤氧化酶抑制测定来测试兰克塔。使用色谱技术在最活跃的提取物上进行生物测定引导的分馏和分离。使用光谱技术测定分离的化合物的结构。 M.Pumilum Var的最活跃的二氯甲烷提取物。叶片叶(IC50?= 161.6?μg/ ml)产生一种新的化合物,3,7-二羟基-5-甲氧基-4,8-​​二甲基 - 异豆素(1),以及五种已知的化合物,Viz。 Ardisia quinone A(2),Maesanin(3),Stigmasterol(4),四糖烷(5)和Margaric acid(6)。发现新化合物是最活性的黄嘌呤氧化酶抑制剂,IC50值为0.66≤0.01≤0.μg/ ml,从阳性对照(IC50)(IC50)的阳性对照(P≥10.05)没有显着差异(p?>〜0.05) ?=?0.24?±0.00?μg/ ml)。该研究表明,新的化合物3,7-二羟基-5-甲氧基-4,8-​​二甲基 - 异壳蛋白(1),其与M.Pumilum Var的二氯甲烷提取物分离。叶子叶,可能是潜在的黄嘌呤氧化酶抑制剂。

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