首页> 外文OA文献 >Synthesis and anticancer properties of 1-(2-isopropyl-5-methylphenoxymethyl)-3R-4-aryl-5,6,7,8-tetrahydro-2,2а,8а-triazacyclopentacdazulene derivatives
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Synthesis and anticancer properties of 1-(2-isopropyl-5-methylphenoxymethyl)-3R-4-aryl-5,6,7,8-tetrahydro-2,2а,8а-triazacyclopentacdazulene derivatives

机译:合成和抗癌特性1-(2-异丙基-5-甲基苯甲基甲基甲基甲基)-3R-4-芳基-5,6,7,8-四氮杂-2,2,2,2,200,8А-三亚佐戊戊基CD氮素衍生物

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摘要

In recent years, attention to itself is attracted to the problem of treatment of cancer that is caused by increase in patients, especially of working age. Therefore, the enlargement of the arsenal of anticancer medicines of a wide spectrum of action is actual.The purpose of the study was to synthesize substances with potentially antitumor properties in a series 1-(2-isopropyl-5-methylphenoxymethyl)-3R-4-aryl-5,6,7,8-tetrahydro-2,2а,8а-triazacyclopenta[cd]azulene derivatives and to study the effect of synthesized compounds on inhibition of growth (or their destruction) of a wide range of cancer.The objects of the study were derivatives of 1-(2-isopropyl-5-methylphenoxymethyl)-3R-4-aryl-5,6,7,8-tetrahydro-2,2а,8а-triazacyclopenta[cd]azulene, which were synthesized by refluxing 3-(2-isopropyl-5-methylphenoxymethyl)-6,7,8,9-tetrahydro-5Н-[1,2,4]triazolo[4,3-a]azepine with с appropriate α-halogenketones in ethyl acetate and further cyclization in an alkaline medium. Использовали данные NMR 1Н spectroscopy data were used. The primary evaluation of anticancer activity was carried out National Cancer Institute of Health, USA within the Development Therapeutic Program.A series of new of 1-(2-isopropyl-5-methylphenoxymethyl)-3R-4-aryl-5,6,7,8-tetrahydro-2,2а,8а-triazacyclopenta[cd]azulene derivatives was synthesized, their structure and purity were confirmed by NMR 1Н spectroscopy. The anticancer activity of the synthesized compounds was studied both at a concentration of 10-5 mol/l and in a concentration gradient of 10-4‒10-8 mol/l in experiments in vivo on cancer cell lines. It is shown that insertion of methyl group into position 3 of heterocyclic system of the basic structure of 4-aryl-5,6,7,8-tetrahydro-2,2a,8a-triazacyclopenta[cd]azulene leads to an increase in the anticancer effect.It is found that the tested compounds showed high anticancer effect on all types of cancer cell lines investigated – leukemia, non-small cell lung cancer, colon cancer, CNS cancer, melanoma, ovarian cancer, renal cancer, prostate cancer and breast cancer.
机译:近年来,对自己的治疗问题引起了患者造成的癌症,特别是工作年龄造成的问题。因此,抗癌药物的扩大了广泛的作用的抗癌药物是实际的。该研究的目的是将具有潜在抗肿瘤性质的物质合成1-(2-异丙基-5-甲基苯甲酰基甲基)-3R-4-芳基-5,6,7,8-四氢-2,2,2,2,2,2,2,2,2,2,2,2,2三氮杂环戊基[Cd]亚祖烯衍生物,并研究合成化合物对抑制种类的生长(或其破坏)的抑制作用。该研究的目的是1-(2-异丙基-5-甲基苯甲基甲基甲基)-3R-4-芳基-5,6,7,8-四氮杂-2,2,2,2,2,2,2,2,2,2,2,2,2,2,2,2,2,2,2,2,2,2,2,20,其是通过回流3-(2-异丙基-5-甲基苯甲氧基甲基)-6,7,8,9-四羟基-5- [1,2,4]三唑唑[4,3-A]偶氮物合成,用载体α-卤素酮乙酸乙酯和进一步环化在碱性介质中。使用использовалиданныеnmr1Н光谱数据。在发展治疗计划中进行了美国国家癌症卫生研究所的抗癌活动的主要评价。合成了一系列新的1-(2-异丙基-5-甲基苯甲基甲基甲基)-3R-4-芳基-5,6,7,8-四亚齐甲戊二醇酯,其结构通过NMR 1-Spectroscopy确认和纯度。在体内癌细胞系中的实验中,在10-5mol / L的浓度下和10-4-10-8mol / L的浓度梯度进行了合成化合物的抗癌活性。结果表明,将甲基插入4-芳基-5,6,7,8-四氢-2,2,2,2,2,8a-tiazacyclopenta [Cd]亚祖族的杂环体系的杂环系统的位置3.亚祖烯导致增加抗癌效果。结果发现,测试的化合物对所有类型的癌细胞系进行了高抗癌影响 - 白血病,非小细胞肺癌,结肠癌,CNS癌,黑素瘤,卵巢癌,肾癌,前列腺癌和乳腺癌。

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