基于氨基胺的新型希夫基:在农业中具有高抗真菌活性
Xin Zhang1, Ming Gao1, Yajie Dong1
1College of Chemistry and Chemical Engineering, Xinjiang Agricultural University, Urumqi, 830052, China.
Chemistry & biodiversity
|August 21, 2024
概括
新的基于氨基库马林的希夫基具有强大的抗真菌活性,可以对抗植物病原体. 与现有的杀菌剂相比,5n和7p化合物显示出更高的疗效,为农业应用提供了潜力.
科学领域:
- 药用化学 医学化学
- 农业科学 农业科学
- 有机合成 有机合成
背景情况:
- 自然产品的结构改造是开发有效杀菌剂的关键.
- 氨基库马林衍生物因其潜在的生物活性而受到探索.
研究的目的:
- 合成和评估一系列基于氨基库马林的新型希夫基的抗真菌特性.
- 为了确定有效的抗真菌剂来控制植物病原菌.
主要方法:
- 基于氨基库马林的希夫基的合成和表征使用NMR和HR-MS.
- 在体外对 Alternaria solani,Fusarium oxysporum,Botrytis cinerea和Alternaria alternata进行抗真菌活性测试,使用菌根生长速度.
- 结构-活性关系 (SAR) 分析以确定抗真菌功效的关键结构特征.
主要成果:
- 大多数合成的化合物显示出显著的抗真菌活性.
- 化合物5b,5c,5d,5h,5n,7c,7n和7p的疗效高于商用杀菌剂甲和氧.
- 在C-3位置的电子撤回组和化甲增强了抗真菌活性.
结论:
- 化合物5n和7p是新型广谱杀菌剂的有希望的化合物.
- 这些化合物显示出农业应用在作物保护方面的潜力.
相关概念视频
Aryldiazonium Salts to Azo Dyes: Diazo Coupling
2.9K
The reaction of weakly electrophilic aryldiazonium (also called arenediazonium) salts with highly activated aromatic compounds leads to the formation of products with an —N=N— link, called an azo linkage. This reaction, presented in Figure 1, is known as diazo coupling and occurs without the loss of the nitrogen atoms of the aryldiazonium salt. Highly activated aromatic compounds such as phenols or arylamines favor the diazo coupling reaction. The coupling generally occurs at the...
2.9K
Physical Properties of Amines
3.0K
Amines with low molecular weight are usually gaseous at room temperature, while those with high molecular weight are liquid or solids in nature. Usually, low molecular weight amines have a rotten fish-like smell. Diamines typically have a pungent smell. For instance, cadaverine and putrescine, depicted in Figure 1, are two molecules responsible for decaying tissue.
3.0K
Amines to Sulfonamides: The Hinsberg Test
3.3K
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...
3.3K


