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从谷精草属植物(谷精草科)中分离得到的化合物及其在抗菌、细胞毒性和抗病毒试验中的评价。

Compounds Isolated from spp. (Eriocaulaceae) and Their Evaluation in Antimicrobial, Cytotoxic, and Antiviral Assays.

作者信息

Moreira Laysa Lanes Pereira Ferreira, Oliveira Lucas Almeida, Conti Raphael, de Almeida Larissa Costa, Costa-Lotufo Leticia V, Micheletti Ana Camila, Dolci Isabela, Fernandes Rafaela Sachetto, Oliva Glaucius, Guido Rafael Victorio Carvalho, Lacerda Valdemar, Borges Keyller Bastos, Borges Warley de Souza

机构信息

Departamento de Química, Universidade Federal Espírito Santo, Avenida Fernando Ferrari 514, Goiabeiras, Vitória, Espírito Santo 29075-910, Brazil.

Departamento de Farmacologia, Universidade de São Paulo, Avenue Prof. Lineu Prestes, 1524, Butantã,São Paulo, São Paulo 05508-000, Brazil.

出版信息

ACS Omega. 2025 Jun 18;10(25):26403-26414. doi: 10.1021/acsomega.4c11026. eCollection 2025 Jul 1.

Abstract

and belong to the Eriocaulaceae family. According to the literature, secondary metabolites isolated in have interesting biological activities. This research aimed to isolate constituents from the capitula of the mentioned species and to evaluate their cytotoxic, antimicrobial, and antiviral activities. Through maceration and several types of separation procedures, the crude extracts were produced, and the structures of constituents were identified mostly by nuclear magnetic resonance. Cytotoxic and antimicrobial activities were evaluated by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide and 2,3,5-triphenyl-2-tetrazolium chloride methods, respectively, while antiviral activity was evaluated by enzymatic and phenotypic assays. Two flavonoids were isolated in the dichloromethane fraction, and four flavonoids and one benzoic acid derivative were isolated in the ethyl acetate fraction of . Paepalantine was isolated from . The isolated compounds did not show significant cytotoxicity, and the highest values of growth-inhibitory activity observed reached 29.17% (colon cancer) and 19.24% (breast cancer). Antimicrobial evaluation showed the best result to 6-methoxykaempferol against (MIC = 250 μg mL). Antiviral evaluation showed that 6-methoxykaempferol-3--β-D-6″-(-coumaroyl)-glucopyranoside inhibited the ZIKV enzyme NS2B-NS3pro in the lowest micromolar range (IC = 1.95 μM); however, it did not show inhibition when evaluated in phenotypic assays with the ZIKV replicon.

摘要

属于谷精草科。根据文献记载,从[具体来源]中分离出的次生代谢产物具有有趣的生物活性。本研究旨在从上述物种的头状花序中分离成分,并评估它们的细胞毒性、抗菌和抗病毒活性。通过浸渍和几种分离程序制备了粗提取物,成分结构大多通过核磁共振进行鉴定。细胞毒性和抗菌活性分别通过3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐和2,3,5-三苯基-2-四氮唑氯化物方法进行评估,而抗病毒活性则通过酶法和表型试验进行评估。在二氯甲烷馏分中分离出两种黄酮类化合物,在[具体物质]的乙酸乙酯馏分中分离出四种黄酮类化合物和一种苯甲酸衍生物。从[具体物质]中分离出了白榈木碱。分离出的化合物未显示出显著的细胞毒性,观察到的生长抑制活性最高值分别为29.17%(结肠癌)和19.24%(乳腺癌)。抗菌评估显示,6-甲氧基山奈酚对[具体微生物]的效果最佳(MIC = 250 μg/mL)。抗病毒评估表明,6-甲氧基山奈酚-3--β-D-6″-(-香豆酰基)-葡萄糖苷在最低微摩尔范围内抑制寨卡病毒酶NS2B-NS3pro(IC = 1.95 μM);然而,在用寨卡病毒复制子进行表型试验评估时,它未显示出抑制作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e962/12223841/dd4fa0e4467e/ao4c11026_0001.jpg

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