关于天然脂的脱酸基希夫衍生物作为潜在的抗真菌剂的研究
Renle Xu1, Jinhang Ma1, Runhe Huang1
1Key Laboratory of Biomass Energy and Material, College of Forestry, Northwest A&F University, Yangling, Shaanxi Province 712100, P. R. China.
Journal of agricultural and food chemistry
|July 11, 2025
概括
一种新的脂基杀菌剂通过破坏真菌结构和抑制关键酶,有效控制菌冠. 这种环保的化合物显示出保护小麦作物的前景.
科学领域:
- 农业化学 农业化学
- 菌类学 菌类学是指菌类学.
- 有机合成 有机合成
背景情况:
- 虫冠状腐烂对全球小麦产量构成重大威胁.
- 开发环保和有效的杀菌剂对于可持续农业至关重要.
- 脂基化合物为新型抗真菌剂提供了潜在的途径.
研究的目的:
- 设计和合成基于Schiff的新型脱乙烯衍生物作为潜在的杀菌剂.
- 评估这些化合物的体外和体内疗效,以对抗*Fusarium pseudograminearum*.
- 阐明最有效衍生品的作用机制.
主要方法:
- 基于Schiff的脱乙烯衍生物的合成.
- 使用FT-IR,NMR (H,C) 和LC-MS进行了表征.
- 在体外抗真菌活性测定对*Fusarium pseudograminearum*.
- 在小麦植物的体内保护作用评估.
- 细胞形态和超结构分析.
- 活性氧物种 (ROS) 的染色.
- 酶活性测定 (SOD,POD,CAT,PPO) 进行.
- 分子对接研究. 分子对接研究.
主要成果:
- 化合物4o (Co. 4o) 在体外显著抑制了*Fusarium pseudograminearum*的生长 (EC50=5.45μg/mL).
- 在小麦植物中,Co. 4o表现出对 fusarium 冠状腐烂的保护作用.
- 显微镜分析显示,在Co. 4o治疗后,真菌菌和超结构受到严重损害.
- 观察到ROS的积累和主要真菌酶 (SOD,POD,CAT,PPO) 的抑制.
- 分子对接表明了Schiff基组和氨基酸之间的键相互作用.
结论:
- 基于Schiff的脱水乙衍生品Co. 4o是一种强大且环保的杀菌剂候选物.
- Co. 4o通过破坏真菌细胞形态,诱导ROS和抑制必需酶来起作用.
- 这种化合物显示出对控制小麦中fusarium皇冠腐烂的显著潜力.
相关概念视频
Preparation of Aldehydes and Ketones from Carboxylic Acid Derivatives
2.8K
Aldehydes are more reactive than carboxylic acids and hence, can get over-reduced to alcohol in the presence of strong reducing agents. Therefore, carboxylic acids are inefficient in preparing aldehydes using LAH.
Carboxylic acid derivatives like acid chlorides and esters are more easily reducible than the corresponding acids. The derivatives reduce in the presence of mild reducing agents to give aldehydes. Aldehydes can also be prepared by Rosenmund reduction, that is, the reduction of...
Carboxylic acid derivatives like acid chlorides and esters are more easily reducible than the corresponding acids. The derivatives reduce in the presence of mild reducing agents to give aldehydes. Aldehydes can also be prepared by Rosenmund reduction, that is, the reduction of...
2.8K
Carboxylic Acid Derivatives: Overview
4.2K
Carboxylic acid derivatives are formed by replacing the hydroxyl group of carboxylic acids with a different functional group. The most common carboxylic acid derivatives are:
4.2K
Amines to Sulfonamides: The Hinsberg Test
3.8K
The Hinsberg test is a method to identify primary, secondary and tertiary amines, named after its pioneer, Oscar Hinsberg. Here, amines are treated with benzenesulfonyl chloride, also known as the Hinsberg reagent, in the presence of an excess of aqueous base, followed by acidification. Based on the nature of the amines, different changes are observed.
Generally, a primary amine reacts with the Hinsberg reagent to produce an N-substituted benzenesulfonamide. The electron-withdrawing...
Generally, a primary amine reacts with the Hinsberg reagent to produce an N-substituted benzenesulfonamide. The electron-withdrawing...
3.8K
Acetals and Thioacetals as Protecting Groups for Aldehydes and Ketones
4.6K
Acetals are formed by reacting two equivalents of alcohol with carbonyl compounds like aldehydes or ketones. Acetals are unaffected by bases, nucleophiles, oxidizing agents, and reducing agents. They serve as protecting groups for aldehydes and ketones. Acetals can be easily formed and also easily removed via mild acid hydrolysis.
In the presence of multiple functional groups, when selective reduction of one group over the other is desired, groups like aldehydes and ketones that form acetals...
In the presence of multiple functional groups, when selective reduction of one group over the other is desired, groups like aldehydes and ketones that form acetals...
4.6K
Alcohols from Carbonyl Compounds: Reduction
10.8K
Reduction is a simple strategy to convert a carbonyl group to a hydroxyl group. The three major pathways to reduce carbonyls to alcohols are catalytic hydrogenation, hydride reduction, and borane reduction.
Catalytic hydrogenation is similar to the reduction of an alkene or alkyne by adding H2 across the pi bond in the presence of transition metal catalysts like Raney Ni, Pd–C, Pt, or Ru. Aldehydes and ketones can be reduced by this method, often under mild to moderate heat (25–100°C) and...
Catalytic hydrogenation is similar to the reduction of an alkene or alkyne by adding H2 across the pi bond in the presence of transition metal catalysts like Raney Ni, Pd–C, Pt, or Ru. Aldehydes and ketones can be reduced by this method, often under mild to moderate heat (25–100°C) and...
10.8K


