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从 Baccharis darwinii Hook & Arn.(菊科)中分离得到的提取物和对香豆素类化合物的抗真菌活性。

Antifungal activity of extracts and prenylated coumarins isolated from Baccharis darwinii Hook & Arn. (Asteraceae).

机构信息

Laboratorio de Productos Naturales Patagónicos (LAPRONAP), Facultad de Ciencias Naturales, Universidad Nacional de la Patagonia San Juan Bosco, Km 4, CP 9000, Comodoro Rivadavia, Chubut, Argentina.

出版信息

Molecules. 2010 Jul 13;15(7):4898-907. doi: 10.3390/molecules15074898.

Abstract

The petroleum ether extract of Baccharis darwinii showed activity against Cryptococcus neoformans and dermatophytes. Bioactivity-guided fractionation of Baccharis darwinii has resulted in the isolation of three coumarins: 5'-hydroxy aurapten (anisocoumarin H, 1), aurapten (7-geranyloxycoumarin, 2) and 5'-oxoaurapten (diversinin, 3). The structures of these compounds were characterized by spectroscopic methods. These compounds were evaluated for their antimicrobialactivity against a panel of each, bacteria and fungi. Compound 3 showed the best activities against Microsporum gypseum, Trichophyton rubrum and Trichophyton mentagrophytes with MICs = 15.6 microg/mL, followed by compound 1 whose MICs against the same fungi were 62.5 microg/mL. In addition they showed fungicidal rather than fungistatic activity. Both compounds showed moderate activity (MICs = 125 microg/mL) against Cryptococcus neoformans. This is the first report of the presence of compound 1 in B. darwinii.

摘要

菊科植物地胆草石油醚提取物对新型隐球菌和皮肤真菌具有活性。菊科植物地胆草的生物活性导向分离得到三种香豆素:5'-羟基当归素(anisocoumarin H,1)、当归素(7-香叶基香豆素,2)和 5'-氧当归素(diversinin,3)。这些化合物的结构通过光谱方法进行了表征。这些化合物针对每种细菌和真菌的抗菌活性进行了评估。化合物 3 对石膏样小孢子菌、红色毛癣菌和须癣毛癣菌的活性最好,MIC 值为 15.6 μg/mL,其次是化合物 1,其对相同真菌的 MIC 值为 62.5 μg/mL。此外,它们表现出杀菌而不是抑菌活性。这两种化合物对新型隐球菌均显示出中等活性(MIC 值为 125 μg/mL)。这是首次在 B. darwinii 中发现化合物 1。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f43/6257657/85e0658c8903/molecules-15-04898-g001.jpg

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