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.

CHUL
2705, boulevard Laurier
T4-50
Québec, Québec
Canada G1V 4G2
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Dionne P, Ngatcha BT, Poirier D

D-ring allyl derivatives of 17 beta- and 17 alpha-estradiols: chemical synthesis and 13C NMR data

Journal Article

Steroids, 62 (10), 1997.

Abstract | Links:

Blomquist CH, Leung BS, Beaudoin C, Poirier D, Tremblay Y

Intracellular regulation of 17 beta-hydroxysteroid dehydrogenase type 2 catalytic activity in A431 cells

Journal Article

J Endocrinol, 153 (3), 1997.

Abstract | Links:

Simard J, Sanchez R, Poirier D, Gauthier S, Singh SM, Merand Y, Belanger A, Labrie C, Labrie F

Blockade of the stimulatory effect of estrogens, OH-tamoxifen, OH-toremifene, droloxifene, and raloxifene on alkaline phosphatase activity by the antiestrogen EM-800 in human endometrial adenocarcinoma Ishikawa cells

Journal Article

Cancer Res, 57 (16), 1997.

Abstract | Links:

Shah GM, Poirier D, Desnoyers S, Saint-Martin S, Hoflack JC, Rong P, ApSimon M, Kirkland JB, Poirier GG

Complete inhibition of poly(ADP-ribose) polymerase activity prevents the recovery of C3H10T1/2 cells from oxidative stress

Journal Article

Biochim Biophys Acta, 1312 (1), 1996.

Abstract | Links:

Poirier D, Mérand Y, Labrie C, Labrie F

D-Ring alkylamine derivatives of estradiol: effect on er-binding affinity and antiestrogenic activity

Journal Article

Bioorg Med Chem Lett, 6 (21), 1996.

Pelletier JD, Poirier D

Synthesis and evaluation of estradiol derivatives with 16 alpha-(bromoalkylamide), 16 alpha-(bromoalkyl) or 16 alpha-(bromoalkynyl) side chain as inhibitors of 17 beta-hydroxysteroid dehydrogenase type 1 without estrogenic activity

Journal Article

Bioorg Med Chem, 4 (10), 1996.

Abstract | Links:

Bydal P, Sam KM, Poirier D

Steroid-hindered 17 beta-tertiary alcohol: characterization of dehydrated compounds

Journal Article

Steroids, 61 (6), 1996.

Abstract | Links:

Tremblay MR, Poirier D

Synthesis of 16-[carbamoyl (bromomethyl)alkyl]-estradiol: a potential dual-action inhibitor designed to blockade estrogen action and biosynthesis

Journal Article

J Chem Soc [Perkin 1], 1996.

Tremblay MR, Auger S, Poirier D

A convenient synthetic method for alpha-alkylation of steroidal 17-ketone : preparation of 16beta(THPO-heptyl)-estradiol

Journal Article

Synth Commun, 25 , 1995.

Tremblay MR, Auger S, Poirier D

Synthesis of 16-(bromoalkyl)-estradiols having inhibitory effect on human placental estradiol 17 beta-hydroxysteroid dehydrogenase (17 beta-HSD type 1)

Journal Article

Bioorg Med Chem, 3 (5), 1995.

Abstract | Links:

246 entries « 22 of 25 »
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Active projects

  • 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
  • Études précliniques avancées pour supporter le développement pharmaceutique d’un dérivé aminostéroïde pour le traitement de cancers résistants à mauvais pronostic, from 2024-06-03 to 2026-05-05
  • Extension de la propriété intellectuelle par l'optimisation des propriétés de l'anticancéreux RM-581, from 2024-05-08 to 2025-07-07
  • Pre-clinical pharmacokinetic and efficacy assays with an efficient 17beta-hydroxysteroid dehydrogenase type 7 inhibitor for breast cancer therapy, from 2024-03-01 to 2025-02-28

Recently finished projects

  • 3alpha-hydroxysteroid dehydrogenase type 3 as a modulator of human adipose tissue function and distribution, from 2020-04-01 to 2024-03-31
  • Investigating TBC1D9 clinical relevance in combination with chemotherapeutic drugs in triple negative breast cancer, from 2023-06-21 to 2024-03-31
  • La conception de nouveaux agents thérapeutiques et la résonance magnétique nucléaire, from 2022-01-01 to 2023-05-31
  • TBC1D9: therapeutic target of the aggressiveness of triple negative breast cancer, from 2023-03-01 to 2024-02-29
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