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9,10-Anthraquinone Dithiocarbamates as Potential Pharmaceutical Substances with Pleiotropic Actions: Computerized Prediction of Biological Activity and Experimental Validation

机译:9,10-蒽醌二硫代氨基磺酸盐作为潜在的药物物质,具有抗性矫正作用:生物活动的计算机化预测和实验验证

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摘要

The pleiotropic pharmacological actions of 9,10-anthraquinone dithiocarbamates were studied. The Way2Drug web portal was used to establish that cytotoxic, antiviral, and anticonvulsant actions were predicted for the study molecules, along with moderate toxicity. In vitro experimental studies showed that all study compounds had cytotoxic effects on tumor cell lines Hep-2, CHO, HeLa, Raji, BL, and B95-8. The high levels of cytotoxicity against cell lines Raji and B95-8 seen with derivatives II, IV, VI, and X was evidence of direct actions on Epstein-Barr virus (EBV). Along with the cytotoxic action, dithiocarbamates V, VIII, and IX showed antiviral effects against herpes virus HSV-2. Compounds VI and X, which had cytotoxic and antiviral actions, produced anticonvulsant effects 3 and 6 h after administration, while dithiocarbamate III, which had cytotoxic activity, retained its antiviral effect 24 h after administration. Dithiocarbamates with pleiotropic actions were moderately toxic (LD50 > 1000 mg/ml, mice, p.o.). Interactions between the structures and the three types of biological activity studied experimentally were assessed.
机译:研究了9,10-蒽醌二硫代氨基甲酸的脂肪药物作用。 Way2drug网站门户网站用于建立细胞毒性,抗病毒和抗惊厥作用,预计研究分子以及中度毒性。体外实验研究表明,所有研究化合物都对肿瘤细胞系Hep-2,Cho,Hela,Raji,BL和B95-8有细胞毒性作用。用衍生物II,IV,VI和X看到的对细胞系Raji和B95-8的高水平细胞毒性是对Epstein-Barr病毒(EBV)的直接作用的证据。随着细胞毒性作用,二硫代氨基甲酸酯V,VIII和IX对疱疹病毒HSV-2的抗病毒作用显示出抗病毒作用。化合物VI和X,其具有细胞毒性和抗病毒作用,在给药后产生抗惊厥作用3和6小时,而具有细胞毒性活性的二硫代氨基甲磺酸III,给药后24小时保留其抗病毒效果。具有抗脂作用的二硫代氨基甲酸酯是适度毒性的(LD50> 1000mg / ml,小鼠,P.O.)。评估结构与三种类型的生物活性之间的相互作用进行了评估。

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