Synthesis, Structural Characterization, and Biological Activities of 1,3,4- Thiadiazole Derivatives Containing Sulfonylpiperazine Structures.
You-Hua LiuFa-Li WangXiao-Li RenChang-Kun LiLin-Hong JinXia ZhouPublished in: Chemistry & biodiversity (2024)
To develop novel bacterial biofilm inhibiting agents, a series of 1,3,4-thiadiazole derivatives containing sulfonylpiperazine structures were designed, synthesized, and characterized using 1 H nuclear magnetic resonance ( 1 H NMR), 13 C nuclear magnetic resonance ( 13 C NMR), and high-resolution mass spectrometry. Meanwhile, their biological activities were evaluated, and the ensuing structure-activity relationships were discussed. The bioassay results showed the substantial antimicrobial efficacy exhibited by most of the compounds. Among them, compound A 24 demonstrated a strong efficacy with an EC 50 value of 7.8 μg/mL in vitro against the Xanthomonas oryzae pv. oryzicola (Xoc) pathogen, surpassing commercial agents thiodiazole copper (31.8 μg/mL) and bismerthiazol (43.3 μg/mL). Mechanistic investigations into its anti-Xoc properties revealed that compound A 24 operates by increasing the permeability of bacterial cell membranes, inhibiting biofilm formation and cell motility, and inducing morphological changes in bacterial cells. Importantly, in vivo tests showed its excellent protective and curative effects on rice bacterial leaf streak. Besides, molecular docking showed that the hydrophobic effect and hydrogen-bond interactions are key factors between the binding of A 24 and AvrRxo1-ORF1. Therefore, these results suggest the utilization of 1,3,4-thiadiazole derivatives containing sulfonylpiperazine structures as a bacterial biofilm inhibiting agent, warranting further exploration in the realm of agrochemical development.
Keyphrases
- magnetic resonance
- biofilm formation
- staphylococcus aureus
- pseudomonas aeruginosa
- candida albicans
- molecular docking
- high resolution
- single cell
- signaling pathway
- high resolution mass spectrometry
- magnetic resonance imaging
- cell therapy
- liquid chromatography
- stem cells
- contrast enhanced
- cystic fibrosis
- mass spectrometry
- oxidative stress
- rectal cancer
- endothelial cells
- cell cycle arrest
- gas chromatography
- cell proliferation
- prognostic factors
- mesenchymal stem cells