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Fungitoxicity of Ortho, Meta and Para-Hydroxybenzalanilines

机译:邻,间和对羟基苯甲酰苯胺的真菌毒性

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摘要

2-Hydroxybenzalaniiines (la-Xla), 3-hydroxybenzalanilines (Ib-Xlb) and 4-hydroxybenzalanilines (Ic-XIc) were synthesized by condensing 2-hydroxybenzaldehyde, 3-hydroxybenzaldehyde and 4-hydroxybenzaldehyde with aniline and substituted anilines in equimolar ratio. The crude products were recrystallized from ethanol and characterized on the basis of elemental analysis and spectral studies. The synthesized hydroxyl substituted benzalanilines were screened in vitro for antifungal potential against Alternaria alternata, Fusarium oxysporum and Myrothecium roridum by spore germination inhibition method at various concentrations. The antifungal potential has been expressed in terms of ED_(50) values.
机译:通过将2-羟基苯甲醛,3-羟基苯甲醛和4-羟基苯甲醛与苯胺和取代的苯胺等摩尔缩合来合成2-羟基苯并丙氨酸(Ia-Xla),3-羟基苯并苯胺(Ib-XIc)和4-羟基苯并苯胺(Ic-XIc)。粗产物从乙醇中重结晶,并在元素分析和光谱研究的基础上进行表征。通过抑制孢子萌发的方法,体外筛选了合成的羟基取代苯并苯胺类化合物对链格孢,尖孢镰刀菌和轮状霉菌的抗真菌潜力。抗真菌潜力已用ED_(50)值表示。

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