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从 Piper regnellii 中分离得到的抗结核新木脂素。

Anti-tuberculosis neolignans from Piper regnellii.

机构信息

Postgraduate Program in Pharmaceutical Sciences, State University of Maringá, Maringá, Paraná, Brazil.

出版信息

Phytomedicine. 2013 May 15;20(7):600-4. doi: 10.1016/j.phymed.2013.01.005. Epub 2013 Mar 7.

Abstract

The present study determined the anti-Mycobacterium tuberculosis activities of supercritical CO2 extracts, neolignans eupomatenoid-5 (1), conocarpan (4) and eupomatenoid-3 (7) and their derivatives (2, 3, 5, 6, and 8) from Piper regnellii, as well as their cytotoxicities. The supercritical CO2 extract from leaves was purified by chromatographic methods, yielding compounds (1), (4) and (7), which were identified by (1)H NMR and comparison with literature data. Anti-M. tuberculosis activity (H37Rv and clinical isolates) was evaluated using a resazurin microtiter assay plate (REMA) to determine the MIC. The cytotoxicity assay was carried out in macrophages J774G.8 by sulforhodamine B colorimetric assay. The supercritical CO2 extracts from leaves and stems, and compound (4) showed activity against M. tuberculosis (MIC 15.6 μg/ml). Compound (1) showed the best activity (MIC 1.9 μg/ml), with good SI. Compounds (7) and (8) showed low activity against M. tuberculosis H37Rv. The derivative compounds did not show increased anti-M. tuberculosis activity. This is the first report, to our knowledge, to describe neolignans from P. regnellii with activity against M. tuberculosis, and compound (1) is a potential candidate for future antituberculosis drugs.

摘要

本研究测定了来自 Piper regnellii 的超临界 CO2 提取物、新木脂素 eupomatenoid-5(1)、conocarpan(4)和 eupomatenoid-3(7)及其衍生物(2、3、5、6 和 8)的抗结核分枝杆菌活性及其细胞毒性。通过色谱方法从叶部分离出超临界 CO2 提取物,得到化合物(1)、(4)和(7),通过 1H NMR 与文献数据进行比较进行鉴定。采用 RESAZURIN 微量滴定板(REMA)测定 MIC,评估抗结核分枝杆菌活性(H37Rv 和临床分离株)。通过磺基罗丹明 B 比色法在巨噬细胞 J774G.8 中进行细胞毒性测定。叶和茎的超临界 CO2 提取物以及化合物(4)显示出对结核分枝杆菌的活性(MIC 15.6 μg/ml)。化合物(1)表现出最佳活性(MIC 1.9 μg/ml),具有良好的 SI。化合物(7)和(8)对结核分枝杆菌 H37Rv 的活性较低。衍生物化合物没有显示出增加的抗结核分枝杆菌活性。据我们所知,这是首次报道来自 Piper regnellii 的新木脂素具有抗结核分枝杆菌活性,化合物(1)是未来抗结核药物的潜在候选物。

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