亲脂性
马来酸酐
琥珀酸酐
马来酸
化学
生物活性
琥珀酸
侧链
立体化学
有机化学
细胞毒性
烷基
生物化学
体外
聚合物
共聚物
作者
Chunguang Han,Hiroyuki Furukawa,Tomohiko Tomura,Ryosuke Fudou,Kenichi Kaida,Bong‐Keun Choi,Genji Imokawa,Makoto Ojika
摘要
Four maleic anhydride derivatives, tricladolides A-D (1-4), and three alkylidene succinic acid derivatives, tricladic acids A-C (5-7), were isolated from the aquatic hyphomycete Tricladium castaneicola. The structures of these compounds were determined by spectroscopic analysis, and all were found to be novel. The compounds exhibited inhibitory activity against fungi, particularly Phytophthora sp., a plant pathogen of oomycetes. The inhibitory activity of these metabolites revealed the importance of the cyclic anhydride structure and the lipophilicity of the alkyl side chain. On the other hand, the cytotoxicity of the compounds against B16 melanoma cells indicated that the cyclic anhydride structure was not essential.
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