含有4-氨基喹唑啉的新型农业杀菌剂苯并肼衍生物的发现、机理研究及安全性评价

IF 6.2 1区 农林科学 Q1 AGRICULTURE, MULTIDISCIPLINARY
Songsong Liu, Hong Li, Sha Li, Mingman Sun and Xiaoping Bao*, 
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引用次数: 0

摘要

基于活性亚基组合法,设计合成了38个含有4-氨基喹唑啉基团的新型苯并肼衍生物,并对其对8种农业植物病原真菌的抑制活性进行了详细的测试。生物测定结果表明,许多合成的化合物在体外对被试真菌表现出非凡的杀真菌活性。例如,化合物A5、A6、A11和A17对炭疽病菌的EC50(半最大有效浓度)分别为0.66、0.71、0.40和0.42 μg/mL,与boscalid (0.36 μg/mL)相当,远优于多菌灵(6.96 μg/mL)。特别重要的是,含有3,4-二氟苯基的化合物A6具有良好的广谱抗真菌作用,对8种真菌的EC50值在0.63 ~ 3.82 μg/mL之间。在200 μg/mL浓度下,化合物A6对水稻纹枯病的治疗和保护效果分别为72.6%和78.9%,高于boscalid(70.7%和65.2%)。此外,通过相对电导率测量、细胞内容物泄漏、荧光显微镜和扫描电镜观察,化合物A6的作用机制研究表明,化合物A6破坏了茄茄的细胞膜完整性。此外,该化合物对茄蚜琥珀酸脱氢酶(SDH)也有较好的抑制作用(最大半数抑制浓度/IC50 = 11.02 μM),略弱于SDH抑制剂boscalid (5.17 μM)。进一步的分子对接分析表明,化合物A6可以通过氢键、静电和π -阳离子相互作用与SDH酶的关键残基形成强相互作用,有望作为靶向SDH的新型杀菌剂先导物。安全性评价表明,化合物A6对水稻和蜜蜂是安全的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Discovery of New Benzohydrazide Derivatives Containing 4-Aminoquinazoline as Effective Agricultural Fungicides, the Related Mechanistic Study, and Safety Assessment

Discovery of New Benzohydrazide Derivatives Containing 4-Aminoquinazoline as Effective Agricultural Fungicides, the Related Mechanistic Study, and Safety Assessment

A total of 38 new benzohydrazide derivatives bearing the 4-aminoquinazoline moiety were designed and synthesized based on the active subunit combination approach and tested in detail for their inhibition activities against eight agricultural phytopathogenic fungi. The bioassay results indicated that many of the synthesized compounds exhibited extraordinary fungicidal activities in vitro against the tested fungi. For example, compounds A5, A6, A11, and A17 had EC50 (half-maximal effective concentration) values of 0.66, 0.71, 0.40, and 0.42 μg/mL against Colletotrichum gloeosporioides, respectively, comparable to that of boscalid (0.36 μg/mL) and much superior to that of carbendazim (6.96 μg/mL). Of particular importance was that compound A6 with a 3,4-difluorophenyl group was found to possess good broad-spectrum antifungal effects, with EC50 values ranging from 0.63 to 3.82 μg/mL against the tested eight fungi. In vivo antifungal assays also revealed that compound A6 had good curative and protective efficacies of 72.6% and 78.9% at 200 μg/mL against Rhizoctonia solani-caused rice sheath blight, higher than those of boscalid (70.7 and 65.2%, respectively). Moreover, the mechanism-of-action studies revealed that compound A6 disrupted the cell membrane integrity of R. solani, as proved by relative conductivity measurements, leakage of cellular contents, fluorescence microscopy, and scanning electron microscopy observations. Significantly, this compound also exhibited an effective inhibition of succinate dehydrogenase (SDH) from R. solani (half-maximal inhibitory concentration/IC50 = 11.02 μM), slightly weaker than that of the SDH inhibitor boscalid (5.17 μM). Further molecular docking analysis revealed that compound A6 could form strong interactions with the key residues of SDH enzyme via hydrogen bond, electrostatic, and π–cation interactions, holding promise for acting as new fungicide leads targeting SDH. Finally, the safety assessments indicated that compound A6 was safe for rice and honeybees.

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来源期刊
Journal of Agricultural and Food Chemistry
Journal of Agricultural and Food Chemistry 农林科学-农业综合
CiteScore
9.90
自引率
8.20%
发文量
1375
审稿时长
2.3 months
期刊介绍: The Journal of Agricultural and Food Chemistry publishes high-quality, cutting edge original research representing complete studies and research advances dealing with the chemistry and biochemistry of agriculture and food. The Journal also encourages papers with chemistry and/or biochemistry as a major component combined with biological/sensory/nutritional/toxicological evaluation related to agriculture and/or food.
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