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黄钟花的抗增殖和抗氧化成分。

Anti-proliferative and antioxidant constituents from Tecoma stans.

作者信息

Marzouk Mohamed, Gamal-Eldeen Amira, Mohamed Mona, El-Sayed Mortada

机构信息

Chemistry of Tannins and Proteins Department, National Research Centre, Dokki, Cairo, Egypt.

出版信息

Z Naturforsch C J Biosci. 2006 Nov-Dec;61(11-12):783-91.

Abstract

Phytochemical investigation of Tecoma stans Juss. fruits and flowers resulted in the isolation of a new phenylethanoid, 2-(3,4-dihydroxyphenyl)ethyl-2-O-[6-deoxy-alpha-L-mannopyranosyl-4-(3,4-dihydroxyphenyl)-2-propenoate]-beta-D-glucopyranoside (3), and a novel monoterpene alkaloid, 5-hydroxy-skytanthine hydrochloride (8), along with eleven known compounds; 4-O-E-caffeoyl-alpha-L-rhamnopyranosyl-(1' --> 3)-alpha/beta-D-glucopyranose (1), E/Z-acetoside (2), isoacetoside (4), rutin (5), luteolin 7-O-beta-D-neohespridoside (6), luteolin 7-O-beta-D-glucopyranoside (7) and sucrose (9) were isolated from the fruits, while luteolin 7-O-beta-D-glucuronopyranoside (10), diosmetin 7-O-beta-D-glucuronopyranoside (11), diosmetin 7-O-beta-D-glucopyranoside (12), diosmetin 7-O-beta-D-glucuronopyranoside methyl ester (13) and acetoside (2) were isolated from the flowers. Their chemical structures have been determined on the basis of chemical and spectroscopic evidences. Biological investigations of a T. stans fruits extract and compounds 1, 2, 4, and 8 indicated that the extract, 1, 2, and 4 possessed a strong scavenging activity to DPPH, peroxyl and hydroxyl radicals. Unlike 4, which potentially induced NO generation in bacterial lipopolysaccharide-stimulated raw murine macrophage (RAW 264.7), the extract, 1, 2, and 8 significantly inhibited the NO generation. The extract, 2 and 4 exhibited a cytotoxic effect on human hepatocarcinoma cells (Hep-G2), while the extract, 2 and 8 were potent growth inhibitors of human breast carcinoma cells (MCF-7). 1 and 2 were remarkable growth inducers of human lymphoblastic leukemia cells (1301), whereas the extract, 2, and 8 stimulated the macrophage proliferation rate. Taken together, the novel compound 8 is effective as anti-proliferative agent against MCF-7 cells and as NO inhibitor, whereas 2 exhibited multi-functional properties as antioxidant and anti-proliferative agent against both solid tumor cell lines Hep-G2 and MCF-7 cells.

摘要

对黄钟花果实和花朵进行植物化学研究,结果分离出一种新的苯乙醇苷,即2-(3,4-二羟基苯基)乙基-2-O-[6-脱氧-α-L-甘露吡喃糖基-4-(3,4-二羟基苯基)-2-丙烯酸酯]-β-D-吡喃葡萄糖苷(3),以及一种新型单萜生物碱,5-羟基-斯堪天新碱盐酸盐(8),还有11种已知化合物;从果实中分离出4-O-E-咖啡酰-α-L-鼠李吡喃糖基-(1'→3)-α/β-D-吡喃葡萄糖(1)、E/Z-乙酰基侧金盏花醇(2)、异乙酰基侧金盏花醇(4)、芦丁(5)、木犀草素7-O-β-D-新橙皮糖苷(6)、木犀草素7-O-β-D-吡喃葡萄糖苷(7)和蔗糖(9),而从花朵中分离出木犀草素7-O-β-D-葡萄糖醛酸苷(10)、香叶木素7-O-β-D-葡萄糖醛酸苷(11)、香叶木素7-O-β-D-吡喃葡萄糖苷(12)、香叶木素7-O-β-D-葡萄糖醛酸苷甲酯(13)和乙酰基侧金盏花醇(2)。它们的化学结构已根据化学和光谱证据确定。对黄钟花果实提取物以及化合物1、2、4和8进行的生物学研究表明,提取物、1、2和4对DPPH、过氧自由基和羟基自由基具有很强的清除活性。与4不同,4在细菌脂多糖刺激的原代小鼠巨噬细胞(RAW 264.7)中可能诱导一氧化氮生成,而提取物、1、2和8显著抑制一氧化氮生成。提取物、2和4对人肝癌细胞(Hep-G2)表现出细胞毒性作用,而提取物、2和8是人类乳腺癌细胞(MCF-7)的有效生长抑制剂。1和2是人类淋巴细胞白血病细胞(1301)显著的生长诱导剂,而提取物、2和8刺激巨噬细胞增殖率。综上所述,新型化合物8作为抗MCF-7细胞增殖剂和一氧化氮抑制剂有效,而2表现出多功能特性,既是抗氧化剂,又是针对实体瘤细胞系Hep-G2和MCF-7细胞的抗增殖剂。

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