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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis of new class of spirocarbocycle derivatives by multicomponent domino reaction and their evaluation for antimicrobial, anticancer activity and molecular docking studies
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Synthesis of new class of spirocarbocycle derivatives by multicomponent domino reaction and their evaluation for antimicrobial, anticancer activity and molecular docking studies

机译:多组分多米诺骨牌反应合成新型螺碳环衍生物及其抗菌,抗癌活性和分子对接研究

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摘要

A series of 25 new spirocarbocycles were synthesized by a three component reaction that involves few cyclic nucleophiles, vinyl malononitriles and aldehydes with variable substitution patterns. All the synthesized compounds were evaluated for their antimicrobial activity and the compounds showed significant activity. Synthesized compounds 4c, 4i and 6i showed good anticancer activity against A549 cancer cell line. Molecular docking studies indicated that compound 4i had the greatest affinity for DNA gyrase receptor than others and compound 6i had the greatest affinity for anaplastic lymphoma kinase (ALK) receptor. These compounds can be better therapeutic agents for microbial and cancer cell lines.
机译:通过三组分反应合成了一系列25个新的螺碳环化合物,该反应涉及很少的环状亲核试剂,乙烯基丙二腈和具有可变取代模式的醛。评价所有合成的化合物的抗微生物活性,并且这些化合物显示出显着的活性。合成的化合物4c,4i和6i对A549癌细胞具有良好的抗癌活性。分子对接研究表明,化合物4i对DNA促旋酶受体的亲和力最大,而化合物6i对间变性淋巴瘤激酶(ALK)受体的亲和力最大。这些化合物可以是用于微生物和癌细胞系的更好的治疗剂。

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