Yamazaki Hiroyuki, Omura Satoshi, Tomoda Hiroshi
Graduate School of Pharmaceutical Sciences, Kitasato University.
Chem Pharm Bull (Tokyo). 2010 Jun;58(6):829-32. doi: 10.1248/cpb.58.829.
A new mitorubrin congener designated 6'-hydroxy-3'-methoxy-mitorubrin (1) was isolated along with structurally related 4'-hydroxy-3'-methoxy-(S)-mitorubrin (2) and monomethyl-(S)-mitorubrin (3) from the culture broth of Penicillium radicum FKI-3765-2 by solvent extraction, octadecyl silyl (ODS) column chromatography and HPLC. The structure of 1 was elucidated by various spectral analyses, including NMR experiments. They have a common isochromane-like ring with a similar hydrophobic side chain. These compounds moderately potentiated miconazole activity against Candida albicans.
从放射青霉FKI-3765-2的培养液中,通过溶剂萃取、十八烷基硅烷(ODS)柱色谱法和高效液相色谱法,分离出一种新的米托菌素同系物,命名为6'-羟基-3'-甲氧基-米托菌素(1),以及结构相关的4'-羟基-3'-甲氧基-(S)-米托菌素(2)和单甲基-(S)-米托菌素(3)。通过包括核磁共振实验在内的各种光谱分析确定了1的结构。它们具有一个带有相似疏水侧链的共同异色满样环。这些化合物适度增强了咪康唑对白色念珠菌的活性。