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来自[具体来源未给出]的新型二萜取代色满基苯醌——波考新的抗寄生虫和细胞毒性活性

Antiparasitic and Cytotoxic Activity of Bokkosin, A Novel Diterpene-Substituted Chromanyl Benzoquinone From .

作者信息

Nvau John B, Alenezi Samya, Ungogo Marzuq A, Alfayez Ibrahim A M, Natto Manal J, Gray Alexander I, Ferro Valerie A, Watson Dave G, de Koning Harry P, Igoli John O

机构信息

Department of Chemistry, Plateau State University, Bokkos, Nigeria.

Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow, United Kingdom.

出版信息

Front Chem. 2020 Nov 17;8:574103. doi: 10.3389/fchem.2020.574103. eCollection 2020.

Abstract

is a medicinal plant growing freely in Nigeria. It is used traditionally to treat tuberculosis, as an anthelmintic and an abortifacient. Phytochemical fractionation and screening of its root extracts has yielded a novel (5-hydroxy-7-methoxy-4-oxo-1-chromanyl)-4-methoxy-p-benzoquinone (breverin)-substituted cassane diterpene, which was designated bokkosin. It was obtained from column chromatography of the ethyl acetate extract of the roots. The compound was characterized using IR, NMR (1D and 2D) and mass spectral data. Promising antiparasitic activity was observed against the kinetoplastid parasite , as well as moderate activity against and and low toxicity in mammalian cells, with the best EC values against (0.69 μg/mL against a standard laboratory strain, and its multi-drug resistant clone (0.33 μg/mL). The effect on in culture was rapid and dose-dependent, leading to apparently irreversible growth arrest and cell death after an exposure of just 2 h at 2 × or 4 × EC. The identification of bokkosin constitutes the first isolation of this class of compound from any natural source and establishes the compound as a potential trypanocide that, considering its novelty, should now be tested for activity against other microorganisms as well.

摘要

是一种在尼日利亚自由生长的药用植物。传统上它被用于治疗肺结核,作为驱虫剂和堕胎药。对其根提取物进行植物化学分离和筛选,得到了一种新型的(5-羟基-7-甲氧基-4-氧代-1-色满基)-4-甲氧基对苯醌(布雷维林)取代的乌苏烷二萜,命名为博科辛。它是从根的乙酸乙酯提取物的柱色谱中获得的。该化合物通过红外光谱、核磁共振(一维和二维)和质谱数据进行表征。观察到该化合物对动质体寄生虫有良好的抗寄生虫活性,对[此处原文缺失两种寄生虫名称]有中等活性,在哺乳动物细胞中的毒性较低,对[此处原文缺失寄生虫名称]的最佳半数有效浓度(EC)值为(对标准实验室菌株为0.69μg/mL,对其多药耐药克隆为0.33μg/mL)。对培养物中[此处原文缺失寄生虫名称]的作用迅速且呈剂量依赖性,在2倍或4倍EC浓度下仅暴露2小时后就导致明显不可逆的生长停滞和细胞死亡。博科辛的鉴定是从任何天然来源首次分离出这类化合物,并将该化合物确立为一种潜在的杀锥虫剂,考虑到其新颖性,现在也应该测试其对其他微生物的活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6041/7705231/2861b6831b4c/fchem-08-574103-g0001.jpg

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