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中国肝叶苔 Ptagiochasm intermedlum L. 中的抗真菌大环双(二苄基)

Antifungal macrocyclic bis(bibenzyls) from the Chinese liverwort Ptagiochasm intermedlum L.

机构信息

School of Pharmaceutical Sciences, Shandong University, Jinan, PR China.

出版信息

Nat Prod Res. 2010 Apr;24(6):515-20. doi: 10.1080/14786410802271587.

Abstract

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.

摘要

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。

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