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Synthesis and Structural Study of Amidrazone Derived Pyrrole-2,5-Dione Derivatives: Potential Anti-Inflammatory Agents. | LitMetric

AI Article Synopsis

  • 1-pyrrole-2,5-dione derivatives possess various pharmacological benefits, particularly in anti-inflammatory and antimicrobial activities.
  • This study focused on synthesizing new 3,4-dimethyl-1-pyrrole-2,5-dione derivatives by reacting amidrazones with dimethylmaleic anhydride and analyzing their properties using techniques like NMR and X-ray diffraction.
  • Findings indicated that these compounds effectively inhibited the proliferation of immune cells and the production of inflammatory cytokines, with the most potent effects observed in specific derivatives.

Article Abstract

1-pyrrole-2,5-dione derivatives are known for their wide range of pharmacological properties, including anti-inflammatory and antimicrobial activities. This study aimed to synthesize new 3,4-dimethyl--pyrrole-2,5-dione derivatives - in the reaction of -substituted amidrazones with 2,3-dimethylmaleic anhydride and evaluate their structural and biological properties. Compounds - were studied by the H-C NMR two-dimensional techniques (HMQC, HMBC) and single-crystal X-ray diffraction (derivatives and ). The anti-inflammatory activity of compounds - was examined by both an anti-proliferative study and a production study on the inhibition of pro-inflammatory cytokines (IL-6 and TNF-α) in anti-CD3 antibody- or lipopolysaccharide-stimulated human peripheral blood mononuclear cell (PBMC) cultures. The antibacterial activity of compounds against , , , , , , and strains was determined using the broth microdilution method. Structural studies of - revealed the presence of distinct and stereoisomers in the solid state and the solution. All compounds significantly inhibited the proliferation of PBMCs in anti-CD3-stimulated cultures. The strongest effect was observed for derivatives -. The strongest inhibition of pro-inflammatory cytokine production was observed for the most promising anti-inflammatory compound .

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9099820PMC
http://dx.doi.org/10.3390/molecules27092891DOI Listing

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