The Interaction Mechanism of Picolinamide Fungicide Targeting on the Cytochrome bc₁ Complex and Its Structural Modification

Abstract

Picolinamide fungicides, structurally related to UK-2A and antimycin-A, bind into the Qi-site in the bc 1 complex. However, the detailed binding mode of picolinamide fungicides remains unknown. In the present study, antimycin-A and UK-2A were selected to study the binding mode of picolinamide inhibitors with four protonation states in the Qi-site by integrating molecular dynamics simulation, molecular docking, and molecular mechanics Generalized Born surface area (MM/GBSA) calculations. Subsequently, a series of new picolinamide derivatives were designed and synthesized to further understand the effects of substituents on the tail phenyl ring. The computational results indicated that the substituted aromatic rings in antimycin-A and UK-2A were the pharmacophore fragments and made the primary contribution when bound to a protein. Compound 9g-hydrolysis formed H-bonds with Hie201 and Ash228 and showed an IC 50 value of 6.05 ± 0.24 μM against the porcine bc 1 complex. Compound 9c, with a simpler chemical structure, showed higher control effects than florylpicoxamid against cucumber downy mildew and expanded the fungicidal spectrum of picolinamide fungicides. The structural and mechanistic insights obtained from the present study will provide a valuable clue for the future designing of new promising Qi-site inhibitors.

Fungicidal Activity of New Pyrrolo[2,3-d]thiazoles and Their Potential Action on the Tryptophan Metabolic Pathway and Wax Biosynthesis

“…However, resistance cannot be avoided when long-term and/or repetitive applications of the same active ingredient or similar products with the same mode of action (MOA) are conducted. To tackle this issue, metyltetraprole was developed, which can overcome the resistance/cross-resistance of other strobilurin fungicides. − …”