Dirar Amina Ibrahim, Wada Mikiyo, Watanabe Takashi, Devkota Hari Prasad
Graduate School of Pharmaceutical Sciences, Kumamoto University, 5-1 Oe-honmachi, Chuo-ku, Kumamoto 862-0973, Japan.
Medicinal, Aromatic Plants and Traditional Medicine Research Institute (MAPTRI), National Center for Research, P.O. Box 2404, Mek Nimr Street, Khartoum 11111, Sudan.
Medicines (Basel). 2019 Nov 22;6(4):113. doi: 10.3390/medicines6040113.
: Pers. (Family: Acanthaceae) is used in traditional medicines as a general tonic and for the treatment of various health problems in Sudan. The main aim of this study was to isolate and identify the major chemical constituents from the aerial parts of B. linariifolia and evaluate their bioactivities. : The dried aerial parts of the plant were extracted successively with 100% acetone and 50% acetone, and thereafter the combined extract was subjected to repeated column chromatography to isolate the main components. Free radical scavenging activity was evaluated using the 1,1-diphenyl-2-picrylhydrazyl (DPPH) free radical method, and in vitro enzyme inhibitory activities against α-glucosidase, pancreatic lipase, and mushroom tyrosinase were evaluated. : From the detailed chemical analysis, verbascoside (), vanillic acid (), apigenin (), and 6''---coumaroylprunin (), were isolated and their structures were identified on the basis of their nuclear magnetic resonance (NMR) spectral data. Among the isolated compounds, verbascoside () showed the most potent free radical scavenging activity (IC = 22.03 ± 0.04 μM). Apigenin () and 6''---coumaroylprunin () showed promising inhibitory activities against all tested enzymes. Apigenin () showed the most potent inhibitory activity against α-glucosidase and tyrosinase (IC = 34.73 ± 1.78 μM and 23.14 ± 1.83 μM, respectively), whereas 6''---coumaroylprunin () showed potent inhibition for lipase (IC = 2.25 ± 0.17 μM). : Four phenolic compounds were isolated and identified from acetone extract, which are reported for the first time from this plant. All compounds showed good DPPH free radical scavenging activities, with verbascoside (1) being the most potent. Apigenin (3) was the most active as α-glucosidase and mushroom tyrosinase inhibitor, while 6''---coumaroylprunin () showed potent inhibitory activity for pancreatic lipase.
假杜鹃(爵床科)在苏丹的传统医学中用作滋补剂,并用于治疗各种健康问题。本研究的主要目的是从亚麻假杜鹃的地上部分分离和鉴定主要化学成分,并评估它们的生物活性。:将植物的干燥地上部分依次用100%丙酮和50%丙酮提取,然后将合并提取物进行反复柱色谱以分离主要成分。使用1,1-二苯基-2-苦基肼(DPPH)自由基法评估自由基清除活性,并评估对α-葡萄糖苷酶、胰脂肪酶和蘑菇酪氨酸酶的体外酶抑制活性。:通过详细的化学分析,分离出了毛蕊花糖苷、香草酸、芹菜素和6''-O-香豆酰基桃叶珊瑚苷,并根据它们的核磁共振(NMR)光谱数据确定了它们的结构。在分离出的化合物中,毛蕊花糖苷表现出最强的自由基清除活性(IC50 = 22.03 ± 0.04 μM)。芹菜素和6''-O-香豆酰基桃叶珊瑚苷对所有测试酶均表现出有前景的抑制活性。芹菜素对α-葡萄糖苷酶和酪氨酸酶表现出最强的抑制活性(IC50分别为34.73 ± 1.78 μM和23.14 ± 1.83 μM),而6''-O-香豆酰基桃叶珊瑚苷对脂肪酶表现出强效抑制作用(IC50 = 2.25 ± 0.17 μM)。:从丙酮提取物中分离并鉴定出四种酚类化合物,这是首次从该植物中报道。所有化合物均表现出良好的DPPH自由基清除活性,其中毛蕊花糖苷活性最强。芹菜素作为α-葡萄糖苷酶和蘑菇酪氨酸酶抑制剂活性最强,而6''-O-香豆酰基桃叶珊瑚苷对胰脂肪酶表现出强效抑制活性。