A Potential Fungicide against Pseudoperonospora cubensis: Design, Synthesis and 3D-QSAR of New Pyrazole-5-carboxamide Derivatives

Background: Downy mildew is one of the major fungi causing significant economic losses to crops. The resistance of this fungus to current fungicides is increasing and new fungi-cides with a unique mode of action are needed. Objective: To find a novel pyrazole amide derivative as a potential fungicide. Methods: A series of pyrazole-5-carboxamide derivatives containing a diaryl ether were de-signed and synthesized by the Intermediate derivatization method (IDM). Their fungicidal activ-ities against Pseudoperonospora Cubensis (P. cubensis, cucumber downy mildew) were evalu-ated in the greenhouse. Results: Bioassays indicated that several compounds exhibited excellent fungicidal activity against P. cubensis in vivo. In particular, T24 (EC50 = 0.88 mg·L-1) had the highest activity compared with Dimethomorph and Fluazinam and other analogues. The relationship between the activity and the structure of these derivatives was analyzed, and an accurate and reliable three-dimensional quantitative structure-activity relationship (3D-QSAR) model was established to determine that electrostatic and steric fields had important effects on the improvement of fun-gicidal activity. Conclusion: The novel pyrazole-5-carboxamide derivative T24 can be considered a potential fungicide for P. cubensis control.