Pierre-Luc Boudreault
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Professor Pierre-Luc Boudreault is a faculty member at Université de Sherbrooke in Canada. His research focuses on medicinal chemistry, particularly the development of novel therapeutic agents, including opioid-free analgesics and antibiotic compounds. Recent publications highlight his work on potassium current blockers for Brugada syndrome and the antibacterial properties of various chemical modifications. His studies integrate structure-activity relationship analyses to address significant challenges in drug development and bacterial resistance.
Recent Grants
Grant: Close
Increasing the capacity and quality of chemical libraries
Open Date: 2022-03-01
Close Date: 2024-04-01
Grant: Close
Optimization of a Brain-Penetrant NTS2 Non-Opioid Analgesic Lead
Open Date: 2022-03-01
Close Date: 2024-04-01
Grant: Close
Antibioswitch : a new class of antibiotics for treating Staphylococcus aureus infections in humans
Open Date: 2022-02-01
Close Date: 2024-02-01
Grant: Close
Start-up Grant
Open Date: 2021-09-01
Close Date: 2023-11-01
Grant: Close
Acuité-Qc Consortium: predicting and visualizing drug action
Open Date: 2021-07-01
Close Date: 2024-06-01
Positions (2)
Pierre-Luc Boudreault
Université de Sherbrooke
4 months ago
A funded PhD student position in Medicinal Chemistry is available in Canada, offered through a collaborative framework between Université de Sherbrooke and Université de Montréal. The research project focuses on organic synthesis, peptide and macrocyclic chemistry, GPCR pharmacology (specifically the ACKR3 receptor), medicinal chemistry, molecular modeling, and structure-activity relationship (SAR) studies. The overarching goal is to develop safer and more effective therapeutic strategies for chronic pain by targeting the ACKR3 GPCR to enhance the body's natural pain-control mechanisms. The project involves solution-phase organic synthesis, solid-phase peptide and macrocyclic synthesis, and molecular modeling to design new molecules. These compounds will be evaluated in vitro for biological activity and tested in vivo in pain models. The candidate will be responsible for the chemistry aspects of the project and will receive interdisciplinary training in medicinal chemistry, molecular modeling, and GPCR pharmacology. The research is highly collaborative, involving biologists and other experts. Supervision is provided by Professor Pierre-Luc Boudreault (Université de Sherbrooke) and Professor Michel Bouvier (Université de Montréal), both recognized for their expertise in medicinal chemistry and pharmacology. The Boudreault Lab is affiliated with the Institut de Pharmacologie de Sherbrooke and several research networks, providing a rich environment for interdisciplinary research and professional development. Applicants should have an MSc in organic chemistry, pharmacy, biochemistry, or a related field, with a strong interest in synthesis, peptide chemistry, and molecular modeling. Good scientific English, writing, and communication skills are required, as is the ability to work in a multidisciplinary team. The position is funded, but specific financial details are not disclosed. The start date is May–June 2026 or earlier. To apply, candidates should send a CV and cover letter to Professor Pierre-Luc Boudreault at [email protected]. More information is available on the lab website: https://www.boudreaultlab.com/.
4 months ago
Pierre-Luc Boudreault
Université de Sherbrooke
4 months ago
The Université de Sherbrooke is offering a PhD position in Medicinal Chemistry, focusing on GPCRs and chronic pain. The research groups, led by Professor Pierre-Luc Boudreault (Université de Sherbrooke) and co-supervised by Professor Michel Bouvier (Université de Montréal), are working on a new therapeutic target to develop safer alternatives to opioids. The project centers on the ACKR3 receptor, a G protein-coupled receptor that modulates the body's pain-relieving mechanisms. By targeting ACKR3, the team aims to restore and enhance natural pain control, providing a promising strategy for chronic pain treatment. The PhD candidate will engage in structure–activity relationship (SAR) studies, solution-phase organic synthesis, solid-phase peptide and macrocyclic synthesis, and molecular modeling. The design and synthesis of new molecules will be supported by molecular modeling, with compounds evaluated in vitro and in vivo for biological activity and pain model efficacy. The candidate will be responsible for the chemistry aspects of the project and will receive interdisciplinary training in medicinal chemistry, molecular modeling, and GPCR pharmacology. Applicants should hold an MSc in organic chemistry, pharmacy, biochemistry, or a related field, and demonstrate knowledge or strong interest in organic synthesis and peptide chemistry. Skills in molecular modeling and a good command of scientific English, writing, and communication are required. The project involves close collaboration with biologists, so the ability to work in a multidisciplinary environment is essential. To apply, candidates should send a CV and cover letter to [email protected]. More information is available at Boudreault Lab . Applications are considered on a rolling basis, with a start date of May–June 2026 or earlier. Only selected candidates will be contacted. Keywords: Medicinal Chemistry, GPCR, Chronic Pain, Organic Synthesis, Peptide Chemistry, Molecular Modeling, Pharmacology, ACKR3 Receptor.
4 months ago
Articles (18)
Year:
2025
Year:
2025
Tomatidine (TO) is a natural narrow-spectrum antibiotic acting on the Staphylococcus aureus small colony variant (SCV) with a minimal inhibitory concentration (MIC) of 0.06 µg/mL while it shows no activity against prototypical strains (MIC > 128 µg/mL). To expand the spectrum of activity of TO, the 3β-hydroxyl group was substituted with an ethane-1,2-diamine, resulting in two diastereoisomers, TM-02 (C3-β) and TM-03 (C3-α). These molecules are equally potent against prototypical S. aureus and E. coli strains (MIC 8 and 32 µg/mL, respectively), whereas TM-02 is more potent against SCV (MIC 0.5 µg/mL) and hyperpermeable E. coli strains (MIC 1 µg/mL). The differences in their modes of action were investigated. We used membrane vesicles to confirm the inhibition of the bacterial ATP synthase, the documented target of TO, and measured effects on bacterial cell membranes. Both molecules inhibited E. coli ATP synthase, with Ki values of 1.1 µM and 3.5 µM for TM-02 and TM-03, respectively, and the bactericidal effect of TM-02 was linked to ATP synthase inhibition. Furthermore, TM-02 had no major effect on the membrane fluidity and gradually reduced membrane potential. In contrast, TM-03 caused structural damages to membranes and completely disrupted the membrane potential (>90%). We were successful in broadening the spectrum of activity of TO. C3-β-diastereoisomers may have more specific antibacterial action than C3-α.
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2024
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2024
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2024
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2024
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2023
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2023
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2023
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2023
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2023
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2022
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2022
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2021
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2021
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2021
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2020
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2020
Collaborators (9)
Antoine Désilets
Professionnel de recherche
Université de Sherbrooke
Sára Ferková
Lecturer
Bishop's University
Taha Azad
Ottawa Hospital Research Institute
Philippe Sarret
Full professor
Université de Sherbrooke
Thomas Castanheiro
University of Rouen
Élie Besserer-Offroy
Adjunct Professor
Université de Sherbrooke
Christine Lavoie
Université de Sherbrooke
François Malouin
Université de Sherbrooke
Mannix Auger-Messier
Full Professor
Université de Sherbrooke
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