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Synthesis, Reactivity, and Anticancer Activity Evaluation of 4-Amino-3-Mercapto-6-Methyl-1,2,4-Triazin-5(4H)-One Derivatives

机译:Synthesis, Reactivity, and Anticancer Activity Evaluation of 4-Amino-3-Mercapto-6-Methyl-1,2,4-Triazin-5(4H)-One Derivatives

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摘要

1,2,4-Triazine and its derivatives occupy a fundamental position in the field of medicinal chemistry because of their diverse biological applications, such as anticancer. To search for promising anticancer agents, a new series of 4-amino-3- mercapto-6-methyl-1,2,4-triazin-5(4H)-one derivatives was prepared. Straightforward synthetic methodologies were employed, such as condensation, cyclization, hydrazinolysis, alkylation, and condensation-addition reactions. All of the new compounds were characterized by a combination of spectral data and elemental analysis. The molecular structures of several compounds on a single crystal X-ray provided confirmation. The anticancer activity was evaluated against three cancer cell lines, which are hepatocellular carcinoma (HEPG-2), colorectal carcinoma (HCT-116) and mammary gland breast cancer (MCF- 7). The results revealed that a representative number of compounds have potent cytotoxicity against HEPG-2, HCT-116 and MCF-7 cell lines with IC50 values ranging from 6.71 to 31.25 μg/mL.
机译:1、2、4-Triazine及其衍生品占据了基本药用领域的地位因为各自不同的生物化学应用程序,如抗癌。有前途的抗癌剂,一个新的系列4-amino-3 -mercapto-6-methyl-1 2 4-triazin-5——(4小时)衍生品。合成方法了,比如缩合、环合、肼解、烷基化,condensation-addition反应。所有的新化合物的特点光谱数据和元素的组合分析。化合物的单晶x射线确认。评估对三个癌症细胞系,肝细胞癌(HEPG-2),结肠直肠癌乳房癌(hct - 116)和乳腺癌症(MCF - 7)。结果表明许多化合物的代表细胞毒性对HEPG-2 hct - 116和MCF-7细胞系的IC50值从6.71到

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