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首页> 外文期刊>Synthetic Communications >N'-(1-([1,1'-biphenyl]-4-yl)ethylidene)-2-cyanoacetohydrazide as scaffold for the synthesis of diverse heterocyclic compounds as prospective antitumor and antimicrobial activities
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N'-(1-([1,1'-biphenyl]-4-yl)ethylidene)-2-cyanoacetohydrazide as scaffold for the synthesis of diverse heterocyclic compounds as prospective antitumor and antimicrobial activities

机译:N' - (1 - ([1,1'-双苯基] -4-基)乙基)-2-氰基丙酰肼作为支架,用于合成各种杂环化合物作为前瞻性抗肿瘤和抗微生物活性

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摘要

In this article, the main target was to study the antitumor and antimicrobial efficacy of new heterocycles conjugated with biphenyl moiety in-vitro. This was implemented by utilizing N'-(1-([1,1'-biphenyl]-4-yl)ethylidene)-2-cyanoacetohydrazide 3 as a material for the synthesis of various heterocyclic compounds. Among of them, some compounds were selected and assayed against two antitumor cell lines as (HepG2) and (HCT-116). Conspicuously, the achieved results showed that compounds 6, 13, and 23 possess significant potency against both cancer cell lines. Particularly, compound 13 exhibited a remarkable efficacy, similar to the standard anticancer drug (doxorubicin), against both cancer cell lines. Noteworthy, compound 13 may serve as a potential anticancer therapeutic drug in the future. On the other hand, In-vitro antifungal and antibacterial activities of selected compounds were assayed and the results indicated that the compound 6 exhibited significant potency against Candida albicans, while compounds 6 and 8 displayed spectacular results for the antibacterial study.
机译:在本文中,主要目标是研究在体外缀合与联苯部分缀合的新杂环的抗肿瘤和抗微生物疗效。这是通过利用N' - (1-([1,1--二苯基] -4-基)亚乙基)-2-氰基丙酰肼3作为用于合成各种杂环化合物的材料来实现的。其中,选择一些化合物并针对两种抗肿瘤细胞系(HEPG2)和(HCT-116)测定。显着地,达到的结果表明,化合物6,13和23对癌细胞系具有显着效力。特别是,化合物13表现出与癌细胞系相似的标准抗癌药物(多柔比星)的显着效果。值得注意的是,化合物13可以作为未来作为潜在的抗癌治疗药物。另一方面,测定了所选化合物的体外抗真菌和抗菌活性,结果表明化合物6表现出对念珠菌蛋白的显着效力,而化合物6和8显示抗菌研究的壮观结果。

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