Frontiers in Chemistry (Mar 2022)

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

  • Long-Sheng Wang,
  • Long-Sheng Wang,
  • Chao Guo,
  • Da Hu,
  • Yan-Xi Zhao,
  • Hui-Hui Liu,
  • Yu-Jia Dong,
  • Shang-Bin Sun,
  • Xing Liu,
  • Kang-Hong Hu,
  • Yan-Hong Wei

DOI
https://doi.org/10.3389/fchem.2022.841151
Journal volume & issue
Vol. 10

Abstract

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A class of iodobenzoyldiazenido-functionalized POMs (TBA)3 [Mo6O18(=N=NCOAr)] (Ar = Ph-o-I (1); Ph-m-I (2); Ph-p-I (3); Ph-3,4-I2(4); Ph-2,3,5-I3(5) (TBA = tetrabutylammonium) were prepared via the refluxing reaction of α-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 L3, L5, 3, and 5 demonstrate potent inhibitory activity against coxsackievirus B3 and low in vitro 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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