François Pedinielli
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
François Pedinielli has a total of 13 co-authors. Here are the top co-authors by number of shared publications:
- Adama Hilou
Laboratoire de Biochimie et de Chimie Appliquée (LABIOCA), Université de Ouagadougou, Ouagadougou 09 BP 848, Burkina Faso
1 shared publication - Anne Davin-Regli
UMR_MD1, U-1261, Faculty of Pharmacy, Aix-Marseille University, INSERM, IRBA, MCT, Marseille, France
1 shared publication Anthony Robert
Université de Reims Champagne-Ardenne, CNRS, ICMR UMR 7312, 51097 Reims, France
1 shared publication- Jean Michel Brunel
Aix Marseille Université, INSERM, SSA, MCT Marseille France
1 shared publication - Jean-Marc Nuzillard
University of Reims Champagne-Ardenne
1 shared publication - Jean-Marie Pagès
INSERM, SSA, Aix-Marseille University, MCT, Faculty of Pharmacy, 13385 Marseille, France
1 shared publication
Latest Publications
- 13 June 2023
- Published by Royal Society of Chemistry (RSC) in The Analyst
- Vol. 148 (14) , 3179-3183
ViscY nuclear magnetic resonance experiments for in situ chemical reaction monitoring under spin diffusion conditions
Viscosity-enhanced spectroscopY (ViscY) offers a new way to analyze complex mixtures of time-varying composition.
- 13 June 2023
- Published by Royal Society of Chemistry (RSC) in The Analyst
- Vol. 148 (14) , 3179-3183
ViscY nuclear magnetic resonance experiments for in situ chemical reaction monitoring under spin diffusion conditions
Viscosity-enhanced spectroscopY (ViscY) offers a new way to analyze complex mixtures of time-varying composition.
- Open Access
- 15 May 2023
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 24 (10) , 8790
Acacia senegal Budmunchiamines as a Potential Adjuvant for Rejuvenating Phenicol Activities towards Escherichia coli-Resistant Strains
The continuous emergence of bacterial resistance alters the activities of different antibiotic families and requires appropriate strategies to solve therapeutic impasses. Medicinal plants are an attractive source for researching alternative and original therapeutic molecules. In this study, the fractionation of natural extracts from A. senegal and the determination of antibacterial activities are associated with molecular networking and tandem mass spectrometry (MS/MS) data used to characterize active molecule(s). The activities of the combinations, which included various fractions plus an antibiotic, were investigated using the “chessboard” test. Bio-guided fractionation allowed the authors to obtain individually active or synergistic fractions with chloramphenicol activity. An LC-MS/MS analysis of the fraction of interest and molecular array reorganization showed that most identified compounds are Budmunchiamines (macrocyclic alkaloids). This study describes an interesting source of bioactive secondary metabolites structurally related to Budmunchiamines that are able to rejuvenate a significant chloramphenicol activity in strains that produce an AcrB efflux pump. They will pave the way for researching new active molecules for restoring the activity of antibiotics that are substrates of efflux pumps in enterobacterial-resistant strains.
- 15 May 2023
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 24 (10) , 8790
Open AccessAcacia senegal Budmunchiamines as a Potential Adjuvant for Rejuvenating Phenicol Activities towards Escherichia coli-Resistant Strains
The continuous emergence of bacterial resistance alters the activities of different antibiotic families and requires appropriate strategies to solve therapeutic impasses. Medicinal plants are an attractive source for researching alternative and original therapeutic molecules. In this study, the fractionation of natural extracts from A. senegal and the determination of antibacterial activities are associated with molecular networking and tandem mass spectrometry (MS/MS) data used to characterize active molecule(s). The activities of the combinations, which included various fractions plus an antibiotic, were investigated using the “chessboard” test. Bio-guided fractionation allowed the authors to obtain individually active or synergistic fractions with chloramphenicol activity. An LC-MS/MS analysis of the fraction of interest and molecular array reorganization showed that most identified compounds are Budmunchiamines (macrocyclic alkaloids). This study describes an interesting source of bioactive secondary metabolites structurally related to Budmunchiamines that are able to rejuvenate a significant chloramphenicol activity in strains that produce an AcrB efflux pump. They will pave the way for researching new active molecules for restoring the activity of antibiotics that are substrates of efflux pumps in enterobacterial-resistant strains.