Paranagama Priyani A, Wijeratne E M Kithsiri, Burns Anna M, Marron Marilyn T, Gunatilaka Malkanthi K, Arnold A Elizabeth, Gunatilaka A A Leslie
SW Center for Natural Products Research and Commercialization, Office of Arid Lands Studies, College of Agriculture and Life Sciences, University of Arizona, 250 E. Valencia Road, Tucson, Arizona 85706-6800, USA.
J Nat Prod. 2007 Nov;70(11):1700-5. doi: 10.1021/np070466w. Epub 2007 Nov 8.
Two new heptaketides, corynesporol (1) and 1-hydroxydehydroherbarin (2), along with herbarin (3) were isolated from an endolichenic fungal strain, Corynespora sp. BA-10763, occurring in the cavern beard lichen Usnea cavernosa. The structures of 1-3 were elucidated from their spectroscopic data. Aerial oxidation of corynesporol (1) yielded herbarin (3). Acetylation of 1 afforded the naphthalene derivative 4, whereas acetylation of 3 gave the corresponding naphthoquinone 6 and dehydroherbarin (5). All compounds were evaluated for their cytotoxicity and ability to inhibit migration of human metastatic breast and prostate cancer cell lines MDA-MB-231 and PC-3M, respectively. Dehydroherbarin (5) inhibited migration of both cell lines at concentrations not toxic to these cell lines. This is the first report of metabolites from an endolichenic fungus.
从生长于洞穴胡须地衣松萝(Usnea cavernosa)中的一种内生真菌菌株——棒孢属(Corynespora)BA - 10763中,分离出了两种新的七肽化合物,棒孢菌素(1)和1 - 羟基脱氢草菌素(2),以及草菌素(3)。通过光谱数据阐明了化合物1 - 3的结构。棒孢菌素(1)的空气氧化产生了草菌素(3)。化合物1的乙酰化得到萘衍生物4,而化合物3的乙酰化得到相应的萘醌6和脱氢草菌素(5)。分别评估了所有化合物对人转移性乳腺癌和前列腺癌细胞系MDA - MB - 231和PC - 3M的细胞毒性及抑制其迁移的能力。脱氢草菌素(5)在对这些细胞系无毒的浓度下抑制了两种细胞系的迁移。这是关于内生真菌代谢产物的首次报道。