首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis, antimicrobial and cytotoxic activities of some 5-arylidene-4-thioxo-thiazolidine-2-ones.
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Synthesis, antimicrobial and cytotoxic activities of some 5-arylidene-4-thioxo-thiazolidine-2-ones.

机译:一些5-亚芳基-4-硫代-噻唑烷-2-酮的合成,抗菌和细胞毒性活性。

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摘要

Several 5-arylidene-4-thioxo-thiazolidine-2-ones (3a-n) were synthesized and evaluated as antimicrobial agents against representative strains, including multidrug-resistant strains of clinical isolates. Also, the antiproliferative activity was evaluated against two human carcinoma cell lines (NCI-H292 and HEp-2). The compounds containing the 5-arylidene subunit presented greater antimicrobial activities against Gram positive bacteria, including the multidrug-resistant clinical isolates, than the 4-thioxo-thiazolidine-2-one. Important SAR information was also gathered, such as the contribution of thiocarbonyl attached at 4-position on the thiazolidine heterocyclic for antimicrobial properties. None of the derivatives exhibited significant antiproliferative activity against the human carcinoma cell lines.
机译:合成了几种5-亚芳基-4-硫代-噻唑烷-2-酮(3a-n​​),并评估了其作为代表菌株的抗菌剂,包括临床分离株的多药耐药菌株。同样,评估了对两种人类癌细胞系(NCI-H292和HEp-2)的抗增殖活性。与4-硫代-噻唑烷-2-酮相比,含有5-芳基亚基的化合物对革兰氏阳性细菌(包括耐多药临床分离株)表现出更大的抗菌活性。还收集了重要的SAR信息,例如噻唑烷杂环上4位连接的硫代羰基对抗菌性能的贡献。这些衍生物均未显示出对人癌细胞系的显着抗增殖活性。

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