School of Pharmaceutical Sciences, Shandong University, Jinan, PR China.
Nat Prod Res. 2010 Apr;24(6):515-20. doi: 10.1080/14786410802271587.
Six macrocyclic bis(bibenzyls) were obtained from the Chinese liverwort Ptagiochasm intermedlum L., and their structures were elucidated as pakyonol (1), neomarchantin A (2), isoriccardin C (3), marchantin H (4), riccardin F (5) and riccardin C (6) on the basis of spectroscopic data and comparison with known compounds. Among them, compounds 3-5 were isolated from this liverwort species for the first time. They possessed in vitro antifungal properties against the fluconazole-sensitive and resistant strains of Candida albicans, with minimum inhibitory concentrations (MICs) ranging from 32 to >512 microg mL(-1). Furthermore, riccardin C was also demonstrated to act as a fungal resistance modifying agent when its combined effect with fluconazole on three resistant strains of C. albicans was investigated. The synergistic or additive activity of riccardin C caused dramatically reduced MICs of fluconazole by at most 256-fold.
从中国产的地钱属植物 Ptagiochasm intermedlum L. 中分离得到 6 个大环双(二苄基)类化合物,根据波谱数据并与已知化合物比较,鉴定为 pakyonol(1)、neomarchantin A(2)、isoriccardin C(3)、marchantin H(4)、riccardin F(5)和 riccardin C(6)。其中,化合物 3-5 为该种地钱属植物中的首次分离得到的新化合物。它们对氟康唑敏感和耐药的白念珠菌具有体外抗真菌活性,最小抑菌浓度(MIC)范围为 32-512 μg/mL。此外,当研究 riccardin C 与氟康唑对 3 株耐药白念珠菌的联合作用时,还发现 riccardin C 具有真菌耐药修饰作用。riccardin C 的协同或相加活性使氟康唑的 MIC 值降低了 256 倍。