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从山黧豆中分离得到的两个新的双环倍半萜及其抗菌、抗氧化、抗酪氨酸酶和细胞毒性活性。

Two new bis-iridoids isolated from Scabiosa stellata and their antibacterial, antioxidant, anti-tyrosinase and cytotoxic activities.

机构信息

Université des frères Mentouri-Constantine, Département de chimie, Laboratoire d'Obtention des Substances Thérapeutiques (LOST), Campus Chaabet-Ersas, 25000 Constantine, Algeria; ICMR-UMR CNRS 7312, Groupe Isolement et Structure, Campus Sciences, Bât. 18, BP 1039, 51687 Reims, France.

ICMR-UMR CNRS 7312, Groupe Isolement et Structure, Campus Sciences, Bât. 18, BP 1039, 51687 Reims, France.

出版信息

Fitoterapia. 2018 Mar;125:41-48. doi: 10.1016/j.fitote.2017.12.018. Epub 2017 Dec 19.

Abstract

This study presents the chemical profile investigation of a 70% ethanol extract obtained from Scabiosa stellata, a medicinal herbaceous traditionally used to treat heel cracks. A C NMR-based dereplication methodology was firstly applied on centrifugal partition chromatography-generated fractions in order to quickly identify the major compounds of the extract. The dereplication process was then completed by semi-preparative high-performance liquid chromatography in order to identify unknown or minor compounds. Two new bis-iridoids, namely 7-O-caffeoyl-sylvestroside I (1) and 7-O-(p-coumaroyl)-sylvestroside I (2), together with ten known compounds (3-12) were isolated. Their structures were elucidated by spectroscopic methods including NMR and HR-ESI-MS. The antibacterial, anti-tyrosinase and DPPH radical scavenging activities of the crude extract, fractions, and isolated compounds were evaluated. A significant antibacterial activity was observed for nine isolated compounds, particularly 1 and 2 which yielded MIC values of 31.2μg/mL against Enterococcus faecalis and 62.5μg/mL against Staphylococcus epidermidis. The cytotoxic activity of these new bis-iridoids was evaluated on a fibrosarcoma cell line (HT1080) and only compound 1 exhibited a moderate cytotoxic activity (IC 35.9μg/mL).

摘要

本研究对传统用于治疗足跟裂的草药蓝蓟的 70%乙醇提取物进行了化学成分分析。首先采用基于 13C NMR 的衍生化方法对离心分配色谱生成的馏分进行快速鉴定,以确定提取物的主要成分。然后通过半制备高效液相色谱法对未知或次要化合物进行鉴定,完成了衍生化过程。从该植物中共分离得到两种新的双裂环烯醚萜,即 7-O-咖啡酰梓醇 I(1)和 7-O-(对香豆酰基)梓醇 I(2),以及 10 种已知化合物(3-12)。通过 NMR 和 HR-ESI-MS 等光谱方法阐明了它们的结构。对粗提取物、馏分和分离得到的化合物进行了抗菌、抗酪氨酸酶和 DPPH 自由基清除活性评价。9 种分离得到的化合物表现出显著的抗菌活性,尤其是化合物 1 和 2,对粪肠球菌和表皮葡萄球菌的 MIC 值分别为 31.2μg/mL 和 62.5μg/mL。这两种新的双裂环烯醚萜对纤维肉瘤细胞系(HT1080)的细胞毒性进行了评价,只有化合物 1 表现出中等的细胞毒性(IC 35.9μg/mL)。

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