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植物化学特征分析、食用芳香植物的体外抗炎、抗糖尿病和细胞毒性活性研究

Phytochemical Characterization, In Vitro Anti-Inflammatory, Anti-Diabetic, and Cytotoxic Activities of the Edible Aromatic Plant; .

机构信息

Department of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, Qassim University, Buraydah 51452, Saudi Arabia.

Department of Pharmacognosy, Faculty of Pharmacy, Al-Azhar University, Cairo 11371, Egypt.

出版信息

Molecules. 2021 Jan 3;26(1):203. doi: 10.3390/molecules26010203.

Abstract

is a medicinal herb that alleviates inflammations and fever. Chromatographic separation, phytochemical characterization, and in vitro biological activities of the plant -hexane extract were conducted for the first time in this study. Six compounds were isolated for the first time from the -hexane fraction of aerial parts and were identified on the bases of NMR and MS analyses as pseudo-taraxaterol (), pseudo-taraxasterol acetate (), 3β-acetoxytaraxaster-20-en-30-aldehyde (), calenduladiol-3--palmitate (), stigmasterol (), and α-tocospiro B (). Compound () was a rare tocopherol-related compound and was isolated for the first time from family Asteraceae, while compound () was isolated for the first time from genus . The total alcoholic extract and -hexane fraction were tested for their anti-inflammatory, antidiabetic, and cytotoxic activities. The -hexane fraction has dose dependent red blood cells (RBCs) membrane stabilization and inhibition of histamine release activities with IC: 60.8 and 72.9 µg/mL, respectively. As antidiabetic activity, the alcoholic extract exerted the most inhibition on the activity of yeast α-glucosidase, with an IC: 76.8 µg/mL. The -hexane fraction showed cytotoxic activity against hepatocarcinoma (HepG-2), breast carcinoma (MCF-7), and prostate carcinoma (PC-3) cell lines with IC: 51.8, 90.8 and 62.2 µg/mL, respectively. In conclusion, the anti-inflammatory effect of might be attributed to the triterpenoid constituents of the -hexane extract of the plant.

摘要

是一种草药,可缓解炎症和发热。本研究首次对该植物的正己烷提取物进行了色谱分离、植物化学特性分析和体外生物活性研究。首次从该植物的正己烷部分分离出 6 种化合物,并根据 NMR 和 MS 分析鉴定为伪蒲公英甾醇()、伪蒲公英甾醇乙酸酯()、3β-乙酰氧基蒲公英甾-20-烯-30-醛()、筋骨草二醇-3--棕榈酸酯()、豆甾醇()和α-生育酚 B()。化合物()是一种罕见的生育酚相关化合物,首次从菊科中分离得到,而化合物()则首次从属中分离得到。总醇提物和正己烷部分均进行了抗炎、抗糖尿病和细胞毒性活性测试。正己烷部分具有依赖于剂量的红细胞(RBC)膜稳定作用,并具有组胺释放抑制活性,IC: 60.8 和 72.9 µg/mL。作为抗糖尿病活性,醇提物对酵母α-葡萄糖苷酶的抑制作用最强,IC: 76.8 µg/mL。正己烷部分对肝癌(HepG-2)、乳腺癌(MCF-7)和前列腺癌(PC-3)细胞系表现出细胞毒性活性,IC: 51.8、90.8 和 62.2 µg/mL。综上所述,抗炎作用可能归因于该植物正己烷提取物中的三萜类成分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1f3/7796184/039c3e8a6bc4/molecules-26-00203-g001.jpg

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