作者:Tsutomu Ishikawa、Tatsuru Saito、Ayako Kurosawa、Toshiko Watanabe、Sakiko Maruyama、Yuh-ichiro Ichikawa、Ryota Yamada、Hiroko Okuzawa、Hiromi Sato、Koichi Ueno
DOI:10.1248/cpb.59.472
日期:——
Preliminary examination for the structure–activity relationship of quinone monooxime derivatives on cytotoxicity against HeLa S3 cell and further trials using eight different cell lines suggested that 2-aryl-6,7-methylenedioxy-1,4-naphthoquinone-1-oxime methyl ethers, carrying 2-methoxy-4,5-methylenedioxyphenyl, 7-methoxy-2-methylbenzofuran-4-yl, and 2-methoxycarbonyl-3,4-dimethoxyphenyl as the 2-aryl substituent, were potential candidates for anti-cancer drugs.
初步研究了醌单肟衍生物对 HeLa S3 细胞的细胞毒性的结构-活性关系,并使用八种不同的细胞系进行了进一步试验,结果表明,2-芳基-6,7-亚甲二氧基-1、4-萘醌-1-肟甲基醚,以 2-芳基取代基为 2-甲氧基-4,5-亚甲二氧基苯基、7-甲氧基-2-甲基苯并呋喃-4-基和 2-甲氧基羰基-3,4-二甲氧基苯基,是潜在的候选抗癌药物。