Chen Liang, Cen Yin-Zhi, Tu Yang-Li, Dai Xiang-Jie, Li Yong-Jun, Yang Xiao-Sheng, Li Lin-Zhen
School of Pharmaceutical Sciences, Guizhou Medical University Guiyang 550025, China Engineering Research Center for the Development and Application of Ethnic Medicine and TCM (Ministry of Education),Guizhou Medical University Guiyang 550004, China State Key Laboratory of Functions and Applications of Medicinal Plants, Guizhou Medical University Guiyang 550004, China.
Engineering Research Center for the Development and Application of Ethnic Medicine and TCM (Ministry of Education),Guizhou Medical University Guiyang 550004, China.
Zhongguo Zhong Yao Za Zhi. 2023 Sep;48(17):4686-4692. doi: 10.19540/j.cnki.cjcmm.20230517.201.
The chemical constituents of the seeds of Moringa oleifera were isolated and purified by using Sephadex LH-20, Toyo-pearl HW-40F, silica gel, ODS, and MCI column chromatography. The structures of compounds were identified by high-resolution mass spectrometry, 1H-NMR, ~(13)C-NMR, HMQC, HMBC, and ~1H-1H COSY, as well as physicochemical properties of compounds and literature data. Twelve compounds were isolated from 30% ethanol fraction of the seeds of M. oleifera and identified as ethyl-4-O-α-L-rhamnosyl-α-L-rhamnoside(1), ethyl-3-O-α-L-rhamnosyl-α-L-rhamnoside(2),(4-hydroxybenzyl)ethyl carbamate(3),(4-aminophenyl)acetic acid(4), ethyl-α-L-rhamnoside(5), methyl-α-L-rhamnoside(6), moringapyranosyl(7), 2-[4-(α-L-rhamnosyl)phenyl]methyl acetate(8), niaziridin(9), 5-hydroxymethyl furfural(10), 4-hydroxybenzeneacetamide(11), and 4-hydroxybenzoic acid(12). Among them, compounds 1 and 2 are two new compounds, compound 3 is a new natural product, and compounds 4-5 were yielded from Moringa plant for the first time. All compounds were evaluated for α-glucosidase inhibitory activity in vitro. Compound 10 showed excellent inhibitory activity with IC_(50) of 210 μg·mL~(-1).
采用葡聚糖凝胶LH - 20、东洋珠HW - 40F、硅胶、ODS和MCI柱色谱法对辣木籽的化学成分进行分离纯化。通过高分辨质谱、¹H - NMR、¹³C - NMR、HMQC、HMBC和¹H - ¹H COSY以及化合物的物理化学性质和文献数据对化合物结构进行鉴定。从辣木籽30%乙醇提取物中分离得到12种化合物,分别鉴定为4 - O-α - L - 鼠李糖基-α - L - 鼠李糖苷乙酯(1)、3 - O-α - L - 鼠李糖基-α - L - 鼠李糖苷乙酯(2)、(4 - 羟基苄基)乙基氨基甲酸酯(3)、(4 - 氨基苯基)乙酸(4)、α - L - 鼠李糖苷乙酯(5)、α - L - 鼠李糖苷甲酯(6)、辣木吡喃糖基(7)、2 - [4 - (α - L - 鼠李糖基)苯基]甲基乙酸酯(8)、尼亚齐立定(9)、5 - 羟甲基糠醛(10)、4 - 羟基苯乙酰胺(11)和4 - 羟基苯甲酸(12)。其中,化合物1和2为两个新化合物,化合物3为新天然产物,化合物4 - 5首次从辣木植物中得到。对所有化合物进行了体外α - 葡萄糖苷酶抑制活性评价。化合物10表现出优异的抑制活性,IC₅₀为210 μg·mL⁻¹。