新型1,3-二苯基脲类化合物的合成及其对福寿螺的杀灭活性

    Synthesis of novel 1,3-diphenylurea derivatives and their molluscicidal activity against Pomacea canaliculata

    • 摘要: 福寿螺(Pomacea canaliculata)是我国南方地区典型外来入侵物种,因适应力和繁殖力强,造成农作物减产,威胁粮食安全。开发绿色无公害的福寿螺杀灭药剂,探究其作用机制,是当前防控外来入侵物种的迫切需求。本研究以苯胺及异氰酸酯类衍生物为起始原料,在溶剂体系中,通过苯胺类与异氰酸酯类衍生物的定向亲核加成反应,合成了10个新型1,3-二苯基脲类化合物N-F-3a~N-F-3e及N-L-6a~N-L-6e,通过室内浸杀试验评估了其灭螺活性;采用苏木精-伊红染色(H&E)观察组织形态学变化; 酶活测试、配体与蛋白分子对接等多种方法探究了其作用机制。结果显示:化合物N-F-3a、N-F-3b、N-L-6a~N-L-6c对福寿螺具有良好的杀灭效果,在10 mg/L下对福寿螺的杀灭率达79.2%以上。其中化合物N-F-3a的活性最好:在5 mg/L下72 h内福寿螺杀灭率达100 %;在20 mg/L下暴露72 h后鲤鱼幼苗存活率达83.3%,比市售传统灭螺药物氯硝柳胺更安全。苏木精-伊红染色(H&E)结果表明:化合物N-F-3a可明显造成福寿螺肝脏损伤,是导致福寿螺死亡的重要因素。经分子对接计算,化合物N-F-3a与磷酸果糖激酶通过氢键、疏水作用、π-π堆积多种作用相结合,结合能为−8.40 kcal/mol,低于N-F-3d的结合能(−8.04 kcal/mol),与灭螺活性结果一致,辅助验证了其杀灭福寿螺的作用机制。综上,化合物N-F-3a显示出优异的福寿螺杀灭效果及良好的生物安全性,有望成为新型福寿螺灭螺候选化合物。

       

      Abstract: Pomacea canaliculata is a typical invasive alien species in southern China. Due to its strong adaptability and fecundity, it causes crop yield reduction and threatens food security. Therefore, the development of environmentally friendly molluscicides against P. canaliculata and the exploration of their action mechanisms are urgent needs for the prevention and control of invasive alien species at present. In this study, aniline and isocyanate derivatives were used as starting materials, and 10 novel 1,3-diphenylurea compounds (N-F-3a to N-F-3e and N-L-6a to N-L-6e) were synthesized via directed nucleophilic addition reaction between aniline and isocyanate derivatives. Their molluscicidal activity was evaluated by laboratory immersion toxicity tests; the changes in tissue morphology were observed by hematoxylin-eosin staining (H&E); and the action mechanisms were explored by multiple methods including enzyme activity assay and ligand-protein molecular docking. The results showed that compounds N-F-3a, N-F-3b, and N-L-6a to N-L-6c exhibited excellent molluscicidal activity against P. canaliculata, with a mortality rate > 79.2% at 10 mg/L. Among them, compound N-F-3a showed the best activity: the mortality rate of P. canaliculata reached 100% within 72 h at 5 mg/L; the survival rate of carp larvae was 83.3% after 72 h of exposure at 20 mg/L, indicating a safer profile than the commercial molluscicide niclosamide. The results of hematoxylin-eosin staining (H&E) indicated that compound N-F-3a could cause significant hepatopancreas damage to P. canaliculata, which was an important factor leading to the death of P. canaliculata. Molecular docking calculations revealed that compound N-F-3a bound to phosphofructokinase through multiple interactions including hydrogen bonds, hydrophobic interactions, and π-π stacking, with a binding energy of -8.40 kcal/mol, which was lower than that of N-F-3d (-8.04 kcal/mol). This result was consistent with the molluscicidal activity data, which assisted in verifying the molluscicidal mechanism of compound N-F-3a against P. canaliculata. In conclusion, compound N-F-3a exhibits excellent molluscicidal efficacy against P. canaliculata and good biosafety, and is thus represents a promising candidate for developing novel molluscicide for P. canaliculata control.

       

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