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首页> 外文期刊>Journal of the Brazilian Chemical Society >A New Strategy for the Synthesis of Nonsymmetrical 3,3’-(Aryl/alkyl-methylene)bis-2-hydroxy-1,4-naphthoquinones and Their Cytotoxic Effects in PC3 Prostate Cancer Cells
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A New Strategy for the Synthesis of Nonsymmetrical 3,3’-(Aryl/alkyl-methylene)bis-2-hydroxy-1,4-naphthoquinones and Their Cytotoxic Effects in PC3 Prostate Cancer Cells

机译:非对称3,3' - (芳基/烷基 - 亚甲基)双-2-羟基-1,4-萘醌合成的新策略及其在PC3前列腺癌细胞中的细胞毒性作用

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A novel method for the synthesis of nonsymmetrical 3,3’-(aryl/alkyl-methylene)bis-2-hydroxy-1,4-naphthoquinones was developed by using the Mannich adduct of naphthoquinone and the reaction with another moiety of 2-hydroxy-1,4-naphthoquinone. This novel method produces for the first time nonsymmetrical 3,3’-(aryl/alkyl-methylene)bis-2-hydroxy-1,4-naphthoquinones. In a preliminary study, these compounds (15c, 15f and 15h) were evaluated regarding their effect over the viability of PC3 metastatic prostate cancer cell using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assays at 100 ?μM. Three of these compounds presented relevant cytotoxic effects at 72 h posttreatment.
机译:通过使用萘醌的甘地醌和2-羟基部分的反应来开发一种新的用于合成非对称3,3' - (芳基/亚甲基)双-2-羟基-1,4-萘醌的新方法。 -1,4-萘醌。这种新方法为第一次非对称3,3' - (芳基/烷基 - 亚甲基)双-2-羟基-1,4-萘醌产生。在初步研究中,通过使用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑鎓溴(1-二苯基四唑鎓溴( MTT)在100?μm处测定。其中三种化合物在72小时后呈现了相关的细胞毒性作用。

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