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