1. Academic Validation
  2. Design, Synthesis, and Biological Activity of Novel Triketone-Containing Phenoxy Nicotinyl Inhibitors of HPPD

Design, Synthesis, and Biological Activity of Novel Triketone-Containing Phenoxy Nicotinyl Inhibitors of HPPD

  • J Agric Food Chem. 2024 May 22;72(20):11321-11330. doi: 10.1021/acs.jafc.3c08705.
Chen-Qing Zhang 1 Shuang Gao 1 Lin Bo 1 Hao-Min Song 1 Li-Ming Liu 1 Mei-Xin Zheng 1 Ying Fu 1 Fei Ye 1
Affiliations

Affiliation

  • 1 Department of Chemistry, College of Arts and Sciences, Northeast Agricultural University, Harbin 150030, China.
Abstract

4-Hydroxyphenylpyruvate dioxygenase (HPPD) is a crucial target Enzyme in albino herbicides. The inhibition of HPPD activity interferes with the synthesis of carotenoids, blocking photosynthesis and resulting in bleaching and necrosis. To develop herbicides with excellent activity, a series of 3-hydroxy-2-(6-substituted phenoxynicotinoyl)-2-cyclohexen-1-one derivatives were designed via active substructure combination. The title compounds were characterized via infrared spectroscopy, 1H and 13C nuclear magnetic resonance spectroscopies, and high-resolution mass spectrometry. The structure of compound III-17 was confirmed via single-crystal X-ray diffraction. Preliminary tests demonstrated that some compounds had good herbicidal activity. Crop safety tests revealed that compound III-29 was safer than the commercial herbicide mesotrione in wheat and peanuts. Moreover, the compound exhibited the highest inhibitory activity against Arabidopsis thaliana HPPD (AtHPPD), with a half-maximal inhibitory concentration of 0.19 μM, demonstrating superior activity compared with mesotrione (0.28 μM) in vitro. A three-dimensional quantitative structure-activity relationship study revealed that the introduction of smaller groups to the 5-position of cyclohexanedione and negative charges to the 3-position of the benzene ring enhanced the herbicidal activity. A molecular structure comparison demonstrated that compound III-29 was beneficial to plant absorption and conduction. Molecular docking and molecular dynamics simulations further verified the stability of the complex formed by compound III-29 and AtHPPD. Thus, this study may provide insights into the development of green and efficient herbicides.

Keywords

4-hydroxyphenylpyruvate dioxygenase; active substructure combination; bioassay; computational chemistry.

Figures
Products
  • Cat. No.
    Product Name
    Description
    Target
    Research Area
  • HY-163559
    HPPD Inhibitor