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
- candida albicans
- pseudomonas aeruginosa
- molecular docking
- high resolution
- single cell
- high resolution mass spectrometry
- signaling pathway
- escherichia coli
- cell therapy
- liquid chromatography
- endothelial cells
- cell cycle arrest
- cell proliferation
- magnetic resonance imaging
- cell death
- transcription factor
- endoplasmic reticulum stress
- prognostic factors
- bone marrow
- structure activity relationship
- gas chromatography
- pi k akt