Dr. Donald Poirier has been a professor at the Department of Molecular Medicine (Faculty of Medicine, Laval University, Québec, Qc) since July 1991 as well as a researcher at the CHU de Québec – Research Center (Québec, Qc). Since 2008, he has also been Director of the Organic Synthesis Service and Co-Director of the Analytical and Medicinal Chemistry Platform.
Professor Poirier received his basic training in organic chemistry (PhD from Laval University, 1980-1985) and subsequently specialized in medicinal chemistry and endocrinology (Postdoctoral studies at the CHUL-Research Center, 1986-1990, CRM fellowship) and more recently in solid phase synthesis of small molecules of therapeutic interest such as steroid derivatives. He is especially interested in the development of steroidogenic enzyme (17b-HSDs, steroid sulfatase, CYP1B1) inhibitors and antitumor agents for the treatment of different cancers (breast, prostate, ovary, pancreatic, and leukemia). As examples, he developed the first non-estrogenic irreversible steroidal inhibitor of 17β-HSD1 for the treatment of breast cancer and endometriosis. He also developed a family of aminosteroid derivatives that inhibited tumor growth in mice for different cancers (breast, ovary, pancreatic, and leukemia).
In addition to the synthesis of small molecules by classical chemistry, he succeeded by developing solid-phase syntheses of C18-steroid (estrane) derivatives as well as C19-steroid (androstane) derivatives that enabled the generation of model libraries of targeted therapeutic compounds. Thus, he developed a diethylsilylacetylenic linker that produces more stable compounds and a sulfamate linker that produces two classes (phenol and sulfamate) of relevant steroidal or nonsteroidal compounds according to cleavage conditions. He is also interested in additional aspects of organic chemistry (synthesis, new methodologies, NMR analysis, etc.) and medicinal chemistry (SAR, molecular modeling, biological assays, etc.). A particularity of his research group is that he is interested in several stages of the development of a new drug: conception, chemical synthesis, in vitro biological tests (enzymatic assays, cell proliferation, etc.) and in vivo (estrogenic activities and androgenic in female and male mice, plasma concentration, metabolic stability, xenografts of cancer cells, etc.).
Professor Poirier has published 220 scientific publications and is the holder of 11 patents and patent applications. He has also been involved in more than 450 oral and poster presentations, as well as conferences as invited speaker.
2705, boulevard Laurier
T4-50
Québec, Québec
Canada G1V 4G2
Latest news
- IRSC : Un financement de près de 8 millions de dollars pour 10 projets de recherche 2022-07-19
- 13 chercheurs du Centre de recherche du CHU de Québec-Université Laval obtiennent 7,6M$ au programme Projet des IRSC 2018-01-26
- Obtention d’un financement des IRSC pour le professeur Donald Poirier 2016-02-23
- De Sainte Maresville, DorianeInternCHUL+1 418-525-4444doriane.de-sainte-maresville.1@ulaval.cadoriane.de-sainte-maresville@crchudequebec.ulaval.ca
2705, boulevard Laurier
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2705, boulevard Laurier
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2705, boulevard Laurier
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2705, boulevard Laurier
T4-50
Québec, Québec
Canada G1V 4G2
Formation of 5α-dihydrotestosterone from 5α-androstane-3α,17β-diol in prostate cancer LAPC-4 cells - Identifying inhibitors of non-classical pathways producing the most potent androgen
Journal ArticleBioorg Med Chem Lett, 30 (2), 2020.
Minor chemical modifications of the aminosteroid derivative RM-581 lead to major impact on its anticancer activity, metabolic stability and aqueous solubility
Journal ArticleEur J Med Chem, 188 , 2020.
Design and synthesis of dansyl-labeled inhibitors of steroid sulfatase for optical imaging
Journal ArticleBioorg Med Chem, 28 (7), 2020.
Multiple catalytic activities of human 17β-hydroxysteroid dehydrogenase type 7 respond differently to inhibitors
Journal ArticleBiochimie, 170 , 2020.
Development of a Gram-Scale Synthesis of PBRM, an Irreversible Inhibitor of 17 beta-Hydroxysteroid Dehydrogenase Type 1
Journal ArticleOrg Process Res Dev, 23 (11), 2019.
Total Synthesis of the Antidiabetic (Type 2) Lipid Mediator Protectin DX/PDX
Journal ArticleJ Org Chem, 84 (2), 2019.
A- and D-Ring Structural Modifications of an Androsterone Derivative Inhibiting 17β-Hydroxysteroid Dehydrogenase Type 3: Chemical Synthesis and Structure-Activity Relationships
Journal ArticleJ Med Chem, 62 (15), 2019.
Antisulfatase, Osteogenic, and Anticancer Activities of Steroid Sulfatase Inhibitor EO-33 in Mice
Journal ArticleJ Med Chem, 62 (11), 2019.
Induction of endoplasmic reticulum stress by aminosteroid derivative RM-581 leads to tumor regression in PANC-1 xenograft model
Journal ArticleInvest New Drugs, 37 (3), 2019.
Isolation and functional characterization of a novel endogenous inverse agonist of estrogen related receptors (ERRs) from human pregnancy urine
Journal ArticleJ Steroid Biochem Mol Biol, 191 , 2019.
Active projects
- 3alpha-hydroxysteroid dehydrogenase type 3 as a modulator of human adipose tissue function and distribution, from 2020-04-01 to 2024-03-31
- Aminosteroid derivatives as a new class of cholesterol homeostasis disruptors for selective treatment of pancreatic cancer: Mechanistic and translational studies, from 2022-10-01 to 2027-09-30
- Investigating TBC1D9 clinical relevance in combination with chemotherapeutic drugs in triple negative breast cancer, from 2023-06-21 to 2024-03-31
- TBC1D9: therapeutic target of the aggressiveness of triple negative breast cancer, from 2023-03-01 to 2024-02-29
Recently finished projects
- Évaluation du potentiel thérapeutique de la protectine DX et d'analogues contre la COVID-19 , from 2020-06-01 to 2022-03-31
- La conception de nouveaux agents thérapeutiques et la résonance magnétique nucléaire, from 2022-01-01 to 2023-05-31
- Un aminostéroïde actif oralement pour traiter les cancers du sein triple négatif, from 2021-09-08 to 2022-03-31