Phytochemicals and biological activities of Macaranga hosei and Macaranga constricta (Euphorbiaceae)

W. Salleh, N. D. A. Razak, F. Ahmad
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引用次数: 3

Abstract

Phytochemicals and biological activities of the leaves of Macaranga hosei and Macaranga constricta have been studied. Fractionation and purification of the extracts of M. hosei afforded two triterpenoids, lupenone (1) and β-sitostenone (2) and two flavonoids, 5-hydroxy-7,4’-dimethoxyflavone (3) and 5-hydroxy-6,7,4’-trimethoxyflavone (4). Three triterpenoids characterized as taraxerone (5), taraxerol (6) and β-amyrin (7) were isolated from M. constricta. The structures of these compounds were established by analysis of their spectroscopic data, as compared to that of reported compounds. Biological activities which include antibacterial, α-glucosidase inhibition and antioxidant were also carried out. The antibacterial activities have demonstrated that all extracts and isolated compounds exhibited weak inhibition against the tested bacterial strains with MIC value exceeded 500 μg/mL. Evaluation of α-glucosidase inhibition activity using ρ-nitrophenyl-ρ-D-glucopyranosidase on extracts exhibited α-glucosidase inhibitory potential. The most potent α-glucosidase activity was exhibited by the petroleum ether extract of M. hosei with inhibitory concentration at 50% (IC50) of 25.3 ppm compared with quercetin (4.5 ppm) and acarbose (12.6 ppm). The antioxidant activity was conducted through DPPH radical scavenging activity and total phenolic content. All the extracts displayed positive results and the methanol extract of M. hosei displayed the highest scavenging activity with scavenging concentration at 50% (SC50) value of 25.8 ppm. The methanol extract of M. hosei also gave the highest total phenol content with 347.7 mg GAE/g.
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大黄姜和大戟姜(大戟科)的植物化学成分及生物活性
本文研究了麦卡兰(Macaranga hosei)和麦卡兰(Macaranga constricta)叶片的植物化学成分和生物活性。从缢草提取物中分离纯化得到两种三萜类化合物:lupenone(1)和β- sitoneone(2),以及两种黄酮类化合物:5-羟基-7,4′-二甲氧基黄酮(3)和5-羟基-6,7,4′-三甲氧基黄酮(4)。从缢草中分离得到三萜类化合物:taraxerone(5)、taraxerol(6)和β-amyrin(7)。这些化合物的结构是通过分析它们的光谱数据来确定的,并与已报道的化合物进行了比较。并进行了抗菌、α-葡萄糖苷酶抑制和抗氧化等生物活性研究。抑菌活性表明,所有提取物和分离化合物对MIC值大于500 μg/mL的细菌均有较弱的抑制作用。ρ-硝基苯-ρ- d -葡萄糖苷酶对提取物α-葡萄糖苷酶抑制活性评价显示α-葡萄糖苷酶抑制潜力。与槲皮素(4.5 ppm)和阿卡波糖(12.6 ppm)相比,石蜡石油醚提取物的α-葡萄糖苷酶活性最高,抑制浓度为50% (IC50),为25.3 ppm。通过DPPH自由基清除能力和总酚含量测定其抗氧化活性。所有提取物均呈阳性,其中鹤尾草甲醇提取物的清除率最高,其50% (SC50)值为25.8 ppm。甲醇提取物总酚含量最高,为347.7 mg GAE/g。
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