Triterpenoid Glycosides from Olax imbricata

N. Vo, Suong Thi Minh Huynh, H. T. Nguyen, H. Dương, P. K. Nguyen
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引用次数: 3

Abstract

Introduction: Olax imbricata, owning antibacterial, antioxidant, and anti-inflammatory activities, has been investigated as one of traditional diabetic plants in Vietnam. In our previous publications on Olax imbricata, the structure analysis of the isolated compounds were reported, including two phenolic compounds, three phenolic glycosidic compounds, a sesquiterpenoid tropolone and 1,2,3,4-tetrahydronaphthalene derivatives. This article described the isolation and structure elucidation of three triterpenoid glycosides isolated from the methanol extract of Olax imbricata growing in Phu Yen province. Additionally, the evaluation of inhibitory activity for a-glucosidase was performed on a pure compound. Method: The methanol extract of this plant applied the chromatographic techniques, including thin-layer chromatography and silica gel column chromatography, led to the isolation of three pure compounds. The structures of three isolated compounds were elucidated by the spectroscopic data, including 1D and 2D NMR spectra in a combination of HRESIMS, and the sugar moieties were elucidated by acid hydrolysis. The a-glucosidase inhibitory assay was applied to a pure compound by the colorimetric method. Results: Three triterpenoid glycosides, namely 3-O-a-L-rhamnopyranosyl-(1->4)-b -D-glucopyranosyl-(1->3)-6′- O-ethyl-b -Dglucuronyl oleanolic acid (1), oleanolic acid 28-O-b -D-glucopyranoside (2) and spergulacin (3) were isolated and elucidated. The compound 2 showed its strong potentiala-glucosidase inhibitory activity with the IC50 value of 56.15+/-1.31 mM. Conclusion: Among them, compound 1 is a new one, the compounds 2 and 3 were isolated for the first time from the genus Olax. The compound 2 exhibited the potential a-glucosidase inhibition activity, contributing to demonstrating the diabetes treatment ability of Olax imbricata in the folklore.  
油葵中的三萜苷
简介:油橄榄具有抗菌、抗氧化和抗炎活性,是越南传统的糖尿病植物之一。在我们之前关于油橄榄的文章中,已经报道了分离化合物的结构分析,包括两个酚类化合物,三个酚类糖苷类化合物,一个倍半萜类tropolone和1,2,3,4-四氢萘衍生物。本文报道了从富阳油葵甲醇提取物中分离得到的3个三萜苷类化合物的结构分析。此外,对纯化合物进行了a-葡萄糖苷酶抑制活性的评价。方法:采用薄层色谱法和硅胶柱色谱法对该植物甲醇提取物进行分离纯化。三个分离化合物的结构通过HRESIMS组合的一维和二维NMR光谱数据进行了解析,糖部分通过酸水解进行了解析。a-葡萄糖苷酶抑制试验应用于纯化合物的比色法。结果:分离并鉴定了3- o -a- l-鼠李糖吡喃基-(1->4)-b - d -葡萄糖吡喃基-(1->3)-6 ' - o -乙基-b -双葡萄糖醛酸齐墩果酸(1)、齐墩果酸28-O-b - d -葡萄糖吡喃苷(2)和斯培古拉星(3)三个三萜苷类化合物。化合物2具有较强的潜在葡萄糖苷酶抑制活性,IC50值为56.15+/-1.31 mM。结论:其中化合物1为新化合物,化合物2和3为首次从油葵属植物中分离得到。化合物2显示出潜在的a-葡萄糖苷酶抑制活性,有助于证明油橄榄在民间对糖尿病的治疗能力。
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