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The synthesis of imidazoles and evaluation of their antioxidant and antifungal activities

机译:咪唑的合成及其抗氧化剂和抗真菌活性的评价

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摘要

Tri- and tetra-substituted imidazole compounds were synthesized through in situ oxidation-condensation in the presence of catalytic amount of H(2)PW(12)O(40)A loaded on the ionic liquid-functionalized magnetic nanoparticles. Then, the antioxidant and antifungal activities of the new imidazoles were evaluated. The effectiveness of the samples as DPPH radical scavengers was confirmed by the measured IC50 values and thiophenyl-containing product showed the best IC50 of 0.12 when compared to the standard ascorbic acid. Moreover, all compounds have antifungal activity against Fusarium oxysporum.
机译:通过在离子液体官能化磁性纳米粒子上的催化量的H(2)PW(12)O(12)(4)αa的存在下,通过原位氧化缩合合成三取代的咪唑化合物。 然后,评估新咪唑的抗氧化剂和抗真菌活性。 通过测量的IC50值证实了样品作为DPPH自由基清除剂的有效性,与标准抗坏血酸相比,含硫代苯基的产品显示最佳的IC50为0.12。 此外,所有化合物都具有针对镰刀镰刀菌的抗真菌活性。

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