Syntheses, Characterizations, and Inhibition Activities Against Coxsackievirus B3 of Iodobenzoic Hydrazide Functionalized Hexamolybdates.

Front Chem

National "111" Center for Cellular Regulation and Molecular Pharmaceutics, Key Laboratory of Fermentation Engineering (Ministry of Education), Hubei Provincial Cooperative Innovation Center of Industrial Fermentation, Hubei Key Laboratory of Industrial Microbiology, Sino-German Biomedical Center, Hubei University of Technology, Wuhan, China.

Published: March 2022

A class of iodobenzoyldiazenido-functionalized POMs (TBA) [MoO(=N=NCOAr)] (Ar = Ph--I ; Ph--I ; Ph--I ; Ph-3,4-I ; Ph-2,3,5-I (TBA = tetrabutylammonium) were prepared the refluxing reaction of -octamolybdates, DCC, and corresponding hydrazides in dry acetonitrile. Their structures were determined by Fourier-transform infrared spectroscopy, ultraviolet-visible spectra, X-ray photoelectron spectroscopy, hydrogen-1 nuclear magnetic resonance, and high-resolution mass spectrometry. Research on the biological activity of title compounds shows that , , and demonstrate potent inhibitory activity against coxsackievirus B3 and low cytotoxic activity against Hep-2 cell lines. The covalent linkage between the iodobenzoyldiazenido components and POMs can enhance the molecular inhibitory efficiency of iodobenzohydrazides.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8968398PMC
http://dx.doi.org/10.3389/fchem.2022.841151DOI Listing

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