Semi-synthesis, α-amylase inhibition, and kinetic and molecular docking studies of arylidene-based sesquiterpene coumarins isolated from Ferula tunetana Pomel ex Batt

Author:

Baccari Wiem1,Saidi Ilyes1,Filali Insaf2,Znati Mansour1,Lazrag Houda3,Tounsi Moncef4,Marchal Axel56,Waffo-Teguo Pierre56,Ben Jannet Hichem1ORCID

Affiliation:

1. University of Monastir, Faculty of Science of Monastir, Laboratory of Heterocyclic Chemistry, Natural Products and Reactivity (LR11ES39), Team: Medicinal Chemistry and Natural Products, Avenue of Environment, 5019 Monastir, Tunisia

2. Department of Chemistry, College of Science and Humanities in Al-Kharj, Prince Sattam bin Abdulaziz University, Al-Kharj 11942, Saudi Arabia

3. University of Monastir, Higher Institute of Biotechnology of Monastir, Laboratory of Genetics, Biodiversity and Bioresources Valuation LR11S41, 5019 Monastir, Tunisia

4. Preparatory Year Deanship, Basic Science Department, Prince Sattam Bin Abdulaziz University, Alkharj 11942, Saudi Arabia

5. Université de Bordeaux, Institut des Sciences de la Vigne et du Vin, EA 4577, Unité de Recherche Œnologie 210 Chemin de Leysotte, CS50008, 33882 Villenave d’Ornon, France

6. Université de Bordeaux, Bordeaux INP, Bordeaux Sciences Agro, UMR 1366 OENOLOGIE, ISVV, 33140 Villenave d’Ornon, France

Abstract

Despite all the significant progress made to enhance the efficacy of the existing bank of drugs used to manage and cure type II diabetes mellitus, there is still a need to explore novel, effective bioactive compounds with fewer side effects.

Funder

Prince Sattam bin Abdulaziz University

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

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