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Green Synthesis Using PEG-400 Catalyst,Antimicrobial Activities,Cytotoxicity and In Silico Molecular Docking of New Carbazole Based on α-Aminophosphonate

机译:使用PEG-400催化剂,抗菌活性,细胞毒性和基于α-氨基磷酸盐的新碳酸盐的硅分子对接中的绿色合成

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摘要

New analog α–amino phosphate series with high yield through an effective and environmentally friendly protocol using the PEG-400 catalyst via Kabachnik-Fields has been reported.They were performed to screen antimicrobial activities by the dish diffusion method,anticancer against MCF-7,A-549,and HeLa human cancer cell lines by MTT assay,and carried out in silico molecular docking by Avogadro,AutoDockTools,Discovery Studio 2019 Client,and Molegro Molecular Viewer packages.The 3c and 3h displayed excellent inhibition against Candida albicans and Saccharomyces cerevisiae fungi,respectively.The molecular docking model indicated the reasonable explanations between the receptor and bioactive compounds in vitro of 3c,3 h,and 3b.The 3c was shown as an excellent inhibitor against Candida albicans,which was a new result in vitro and in silico molecular docking model.The 3c,3f,and 3i pointed out excellent inhibitions against HeLa cell lines and new anticancer results of α–amino phosphate compounds.The docking studies of structures against receptors of three human cancer cell lines were conducted and recommended that the hydrogen bonds only formed from active sites of receptors to oxygen atom of the ethoxy group,nitrogen and hydrogen atoms of N-H group,oxygen atom of the P=O double bond group,and the fluorine atoms of the CF3 group in 3i for calculated docking of the receptors of bacteria,fungi,and cancer cell lines to all ligands.
机译:据报道,通过使用Kabachnik-Fields使用PEG-400催化剂的有效且对环境友好的方案,新的模拟α-氨基磷酸盐系列已通过Kabachnik-Fields进行。进行。通过针对MCF-7,抗药性方法,抗微生物的抗菌活性,以筛选抗菌活性。 A-549和MTT分析的HELA人类癌细胞系,并在Avogadro,Autodocktools,Discovery Studio 2019客户端和Molegro Molecular Chiever套件中在硅分子对接中进行。3C和3H对念珠菌和糖含量塞氏丝菌塞氏念珠菌和3H表现出极好的抑制作用。分子对接模型分别表明受体和生物活性化合物在3c,3 h和3b中的合理解释。3C显示为对念珠菌白色念珠菌的极好抑制剂,这是体外和IN的新结果。硅分子对接模型。3C,3F和3i指出了对HELA细胞系的极好抑制作用和α-氨基磷酸化合物的新抗癌结果对针对三种人类癌细胞系的受体的结构进行的对接研究,并建议仅从受体的活性位点形成的氢键,直到乙氧基原子,N-H组的氮原子和氧原子的氧原子,P的氧原子,P = o双键组,以及3i中CF3组的氟原子,用于计算所有配体的细菌,真菌和癌细胞系的受体对接。

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