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The catalytic influence of phosphotungstic acid-functionalized Fe(3)O(4) MNPs blended with TiO(2) on the synthesis of novel spiro-acridines and the evaluation of their medicinal potential through molecular docking studies

This manuscript describes an effective and rapid three-component synthesis of a novel series of spiro-acridine derivatives by integrating the pharmacologically dynamic hydantoin–phenytoin as the prime synthetic equivalent. The process was accelerated by Fe(3)O(4)@TiO(2)-PTA magnetic nanoparticles (M...

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Detalles Bibliográficos
Autores principales: Potdar, Shweta, Pal, Nikita, Sharma, Pratibha, Kumar, Ashok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9058500/
https://www.ncbi.nlm.nih.gov/pubmed/35517166
http://dx.doi.org/10.1039/d0ra06975b
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author Potdar, Shweta
Pal, Nikita
Sharma, Pratibha
Kumar, Ashok
author_facet Potdar, Shweta
Pal, Nikita
Sharma, Pratibha
Kumar, Ashok
author_sort Potdar, Shweta
collection PubMed
description This manuscript describes an effective and rapid three-component synthesis of a novel series of spiro-acridine derivatives by integrating the pharmacologically dynamic hydantoin–phenytoin as the prime synthetic equivalent. The process was accelerated by Fe(3)O(4)@TiO(2)-PTA magnetic nanoparticles (MNPs), which acted as the heterogeneous catalytic system, under ultrasonic conditions. The reaction was performed in the green PEG-200 solvent under aerophilic conditions to obtain products with excellent yields. The characteristics of the synthesized magnetic nano-catalysts were corroborated through powder X-ray diffraction (PXRD), field emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray spectroscopy (EDAX), FT-IR, and VSM techniques. In addition, the structures of the synthesized compounds were ascertained on the basis of elemental analyses and spectro-analytical data ((1)H NMR, (13)C NMR, and mass spectrometry). High yields, smaller E-factor, considerable atom economy, easy recovery, and recyclability of the catalyst and solvent are the captivating features of the developed protocol. Moreover, in view of the ongoing global research on COVID-19, herein, we tried to identify the potential sites of the synthesized moiety that can suitably fit the receptor sites of the main protease of SARS-CoV-2 (SARS-CoV-2 M(pro)).
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spelling pubmed-90585002022-05-04 The catalytic influence of phosphotungstic acid-functionalized Fe(3)O(4) MNPs blended with TiO(2) on the synthesis of novel spiro-acridines and the evaluation of their medicinal potential through molecular docking studies Potdar, Shweta Pal, Nikita Sharma, Pratibha Kumar, Ashok RSC Adv Chemistry This manuscript describes an effective and rapid three-component synthesis of a novel series of spiro-acridine derivatives by integrating the pharmacologically dynamic hydantoin–phenytoin as the prime synthetic equivalent. The process was accelerated by Fe(3)O(4)@TiO(2)-PTA magnetic nanoparticles (MNPs), which acted as the heterogeneous catalytic system, under ultrasonic conditions. The reaction was performed in the green PEG-200 solvent under aerophilic conditions to obtain products with excellent yields. The characteristics of the synthesized magnetic nano-catalysts were corroborated through powder X-ray diffraction (PXRD), field emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray spectroscopy (EDAX), FT-IR, and VSM techniques. In addition, the structures of the synthesized compounds were ascertained on the basis of elemental analyses and spectro-analytical data ((1)H NMR, (13)C NMR, and mass spectrometry). High yields, smaller E-factor, considerable atom economy, easy recovery, and recyclability of the catalyst and solvent are the captivating features of the developed protocol. Moreover, in view of the ongoing global research on COVID-19, herein, we tried to identify the potential sites of the synthesized moiety that can suitably fit the receptor sites of the main protease of SARS-CoV-2 (SARS-CoV-2 M(pro)). The Royal Society of Chemistry 2020-12-16 /pmc/articles/PMC9058500/ /pubmed/35517166 http://dx.doi.org/10.1039/d0ra06975b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Potdar, Shweta
Pal, Nikita
Sharma, Pratibha
Kumar, Ashok
The catalytic influence of phosphotungstic acid-functionalized Fe(3)O(4) MNPs blended with TiO(2) on the synthesis of novel spiro-acridines and the evaluation of their medicinal potential through molecular docking studies
title The catalytic influence of phosphotungstic acid-functionalized Fe(3)O(4) MNPs blended with TiO(2) on the synthesis of novel spiro-acridines and the evaluation of their medicinal potential through molecular docking studies
title_full The catalytic influence of phosphotungstic acid-functionalized Fe(3)O(4) MNPs blended with TiO(2) on the synthesis of novel spiro-acridines and the evaluation of their medicinal potential through molecular docking studies
title_fullStr The catalytic influence of phosphotungstic acid-functionalized Fe(3)O(4) MNPs blended with TiO(2) on the synthesis of novel spiro-acridines and the evaluation of their medicinal potential through molecular docking studies
title_full_unstemmed The catalytic influence of phosphotungstic acid-functionalized Fe(3)O(4) MNPs blended with TiO(2) on the synthesis of novel spiro-acridines and the evaluation of their medicinal potential through molecular docking studies
title_short The catalytic influence of phosphotungstic acid-functionalized Fe(3)O(4) MNPs blended with TiO(2) on the synthesis of novel spiro-acridines and the evaluation of their medicinal potential through molecular docking studies
title_sort catalytic influence of phosphotungstic acid-functionalized fe(3)o(4) mnps blended with tio(2) on the synthesis of novel spiro-acridines and the evaluation of their medicinal potential through molecular docking studies
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9058500/
https://www.ncbi.nlm.nih.gov/pubmed/35517166
http://dx.doi.org/10.1039/d0ra06975b
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