Songsong Liu, Hong Li, Sha Li, Mingman Sun and Xiaoping Bao*,
{"title":"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","authors":"Songsong Liu, Hong Li, Sha Li, Mingman Sun and Xiaoping Bao*, ","doi":"10.1021/acs.jafc.4c0946110.1021/acs.jafc.4c09461","DOIUrl":null,"url":null,"abstract":"<p >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 <b>A5</b>, <b>A6</b>, <b>A11</b>, and <b>A17</b> had EC<sub>50</sub> (half-maximal effective concentration) values of 0.66, 0.71, 0.40, and 0.42 μg/mL against <i>Colletotrichum gloeosporioides</i>, 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 <b>A6</b> with a 3,4-difluorophenyl group was found to possess good broad-spectrum antifungal effects, with EC<sub>50</sub> values ranging from 0.63 to 3.82 μg/mL against the tested eight fungi. In vivo antifungal assays also revealed that compound <b>A6</b> had good curative and protective efficacies of 72.6% and 78.9% at 200 μg/mL against <i>Rhizoctonia solani</i>-caused rice sheath blight, higher than those of boscalid (70.7 and 65.2%, respectively). Moreover, the mechanism-of-action studies revealed that compound <b>A6</b> disrupted the cell membrane integrity of <i>R. solani</i>, 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 <i>R. solani</i> (half-maximal inhibitory concentration/IC<sub>50</sub> = 11.02 μM), slightly weaker than that of the SDH inhibitor boscalid (5.17 μM). Further molecular docking analysis revealed that compound <b>A6</b> 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 <b>A6</b> was safe for rice and honeybees.</p>","PeriodicalId":41,"journal":{"name":"Journal of Agricultural and Food Chemistry","volume":"73 5","pages":"2830–2841 2830–2841"},"PeriodicalIF":6.2000,"publicationDate":"2025-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Discovery of New Benzohydrazide Derivatives Containing 4-Aminoquinazoline as Effective Agricultural Fungicides, the Related Mechanistic Study, and Safety Assessment\",\"authors\":\"Songsong Liu, Hong Li, Sha Li, Mingman Sun and Xiaoping Bao*, \",\"doi\":\"10.1021/acs.jafc.4c0946110.1021/acs.jafc.4c09461\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >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 <b>A5</b>, <b>A6</b>, <b>A11</b>, and <b>A17</b> had EC<sub>50</sub> (half-maximal effective concentration) values of 0.66, 0.71, 0.40, and 0.42 μg/mL against <i>Colletotrichum gloeosporioides</i>, 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 <b>A6</b> with a 3,4-difluorophenyl group was found to possess good broad-spectrum antifungal effects, with EC<sub>50</sub> values ranging from 0.63 to 3.82 μg/mL against the tested eight fungi. In vivo antifungal assays also revealed that compound <b>A6</b> had good curative and protective efficacies of 72.6% and 78.9% at 200 μg/mL against <i>Rhizoctonia solani</i>-caused rice sheath blight, higher than those of boscalid (70.7 and 65.2%, respectively). Moreover, the mechanism-of-action studies revealed that compound <b>A6</b> disrupted the cell membrane integrity of <i>R. solani</i>, 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 <i>R. solani</i> (half-maximal inhibitory concentration/IC<sub>50</sub> = 11.02 μM), slightly weaker than that of the SDH inhibitor boscalid (5.17 μM). Further molecular docking analysis revealed that compound <b>A6</b> 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. 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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.
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.