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突尼斯窄叶芒柄花根部生物活性化合物的分离与结构解析

Isolation and structure elucidation of bioactive compounds from the roots of the Tunisian Ononis angustissima L.

作者信息

Ghribi Lotfi, Waffo-Téguo Pierre, Cluzet Stéphanie, Marchal Axel, Marques Jessica, Mérillon Jean-Michel, Ben Jannet Hichem

机构信息

Laboratory of Heterocyclic Chemistry, Natural Products and Reactivity, Team: Medicinal Chemistry and Natural Products, Faculty of Science of Monastir, University of Monastir, Avenue of Environment, 5019 Monastir, Tunisia.

Univ. de Bordeaux, ISVV, EA 3675 GESVAB, 33140 Villenave d'Ornon, France.

出版信息

Bioorg Med Chem Lett. 2015 Sep 15;25(18):3825-30. doi: 10.1016/j.bmcl.2015.07.076. Epub 2015 Jul 26.

Abstract

A phytochemical investigation of the roots of Ononis angustissima L. (Fabaceae) offered to the bio-guided isolation of new isoflavone 3-(4-(glucopyranosyloxy)-5-hydroxy-2-methoxyphenyl)-7-hydroxy-4H-chromen-4-one 1, together with nine known compounds, ononin 2, formononetin 3, (+)-puerol A-2'-O-β-D-glucose 4, (-)-puerol B-2'-O-β-D-glucopyranose ((-)-sophoraside A) 5, (+)-puerol A 6, (-)-trifolirhizin 7, (-)-trifolirhizin-6'-O-malonate 8, (-)-maackiain 9 and (-)-medicarpin 10. Compounds 2-10 were isolated and identified for the first time in Ononis angustissima. We investigated antioxidant capacities of isolated molecules and results showed that compound 6 exhibited the highest antioxidant activity with IC50 values of 19.53 μg/mL, 28.29 μg/mL and 38.53 μg/mL by DPPH radical, ABTS radical cation and reducing power assay, respectively, and an interesting IC50 (20.45 μg/mL) of 1 against DPPH. In addition, the neuroprotective activity of six isolated molecules (4-7, 9, 10) were evaluated. Following the exposure of PC12 cells to Aβ25-35, compounds 9 and 10 triggered a significant increase of cell viability and in a dose dependent manner.

摘要

对窄叶芒柄花(豆科)根部进行植物化学研究,实现了新异黄酮3-(4-(吡喃葡萄糖氧基)-5-羟基-2-甲氧基苯基)-7-羟基-4H-色原酮-4-酮(1)以及9种已知化合物芒柄花苷(2)、刺芒柄花素(3)、(+)-葛缕酮A-2'-O-β-D-葡萄糖苷(4)、(-)-葛缕酮B-2'-O-β-D-吡喃葡萄糖苷((-)-槐糖苷A)(5)、(+)-葛缕酮A(6)、(-)-三叶豆紫檀苷(7)、(-)-三叶豆紫檀苷-6'-O-丙二酸酯(8)、(-)-紫铆因(9)和(-)-美迪紫檀素(10)的生物导向分离。化合物2 - 10首次在窄叶芒柄花中分离鉴定。我们研究了分离得到的分子的抗氧化能力,结果表明化合物6表现出最高的抗氧化活性,通过DPPH自由基、ABTS自由基阳离子和还原能力测定,其IC50值分别为19.53 μg/mL、28.29 μg/mL和38.53 μg/mL,对DPPH的IC50值为有趣的20.45 μg/mL。此外,评估了6种分离分子(4 - 7、9、10)的神经保护活性。在PC12细胞暴露于Aβ25 - 35后,化合物9和10以剂量依赖方式显著提高了细胞活力。

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