29 avril 2025
Setif1- University Ferhat ABBAS
Fuseau horaire Africa/Algiers

Antifungal Activity of Newly Synthesized Symmetric and Asymmetric Azines: An Experimental and In Silico Study.

Non programmé
20m
Auditorium Mouloud Kacem Nait BELKACEM (Setif1- University Ferhat ABBAS)

Auditorium Mouloud Kacem Nait BELKACEM

Setif1- University Ferhat ABBAS

Campus El Bez, Algiers Road, Setif 19137, Algeria
Synthesis of organic compounds and materials.

Orateur

khadidja FADLI (Laboratoire de Chimie, Ingénierie Moléculaire et Nanostructures, Université Ferhat Abbas Sétif 1, Sétif, Algeria.)

Description

The advancements in modern therapeutics are a direct result of numerous research efforts, which have been developed in the fields of synthesis, analysis, and control of pharmaceutical products.
In recent years, it has been demonstrated that organic compounds containing azomethine groups are important compounds in chemistry, biochemistry, and coordination chemistry due to their flexibility, ease of preparation, exceptional chelating ability, and broad spectrum of biological and pharmaceutical activities, such as antimicrobial, anti-inflammatory, and anticancer properties. Consequently, the chemistry of Schiff bases has always been a promising area of research.
In this context, we are interested in synthesizing new symmetric and asymmetric azines through the reaction of hydrazine with carbonyl derivatives, and the characterization of the obtained products will be carried out using IR and UV-Vis spectroscopic methods, as well as proton and carbon NMR and single-crystal X-ray diffraction (XRD) at 100 K. Furthermore, a biological evaluation will be performed to assess the potential application of our synthesized compounds in the pharmaceutical field. In this study, we conducted an antifungal test against the FOL fungus, and the results showed that our products exhibited remarkable inhibitory activity. Additionally, isovanillin azine was evaluated in silico for its inhibitory activity against the HTLV-1 protease (2B7F) and showed potential as an anticancer drug.

Author

khadidja FADLI (Laboratoire de Chimie, Ingénierie Moléculaire et Nanostructures, Université Ferhat Abbas Sétif 1, Sétif, Algeria.)

Documents de présentation

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