Dr. Sébastien Fortin
Faculty of
Pharmacy
Université Laval,
Canada
CHU de Québec
Research Center, Canada
Assistant
professor
Email: sebastien.fortin@pha.ulaval.ca
Qualifications
2010 Ph.D., Medicinal Chemistry, Université Laval, Canada
2010 Ph.D., Medicinal Chemistry, Université d’Auvergne 1, France
2005 M.Sc., Medicinal Chemistry, Université Laval, Canada
2003 B.Sc., Chemistry, Université Laval
Publications
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Chavez Alvarez, A. C., Bouzriba, C., Ouellette, V., Gagné-Boulet, M., Patenaude, A., Pilote, S., C.-Gaudreault, R., Simard, C., & Fortin, S. (2025). Toxicity, Half-Life and Antitumor Activity of Phenyl 4-(2-Oxo-3-alkylimidazolidin-1-yl)benzenesulfonates as Novel Antimitotic CYP1A1-Targeted Prodrugs in Female Mouse Models. Pharmaceutics, 17(2), 233. https://doi.org/10.3390/pharmaceutics17020233
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Alvarez, A., Bouzriba, C., Bernier, L. et al. Development of an UHPLC-UV Method for Quantification of Three Phenyl 4-(2-oxo-3-alkylimidazolidin-1-yl)benzenesulfonates in CD-1® IGS Female Mouse Plasma. J Anal Chem 79, 456–463 (2024). https://doi.org/10.1134/S1061934824040026
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Gagné-Boulet, M., Bouzriba, C., Chavez Alvarez, A. C., & Fortin, S. (2022). Preparation and biological evaluation of new antimicrotubule agents: Modification of the imidazolidin-2-one moiety of phenyl 4-(2-oxoimidazolidin-1-yl)benzenesulfonates. Chemical Biology & Drug Design, 99, 187–196. https://doi.org/10.1111/cbdd.13971
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Vincent Ouellette, Atziri Corin Chavez Alvarez, Sébastien Fortin; Abstract 284: Design, synthesis and biological evaluation of novel water-soluble salts of the antimitotic prodrugs 4-(3-alkyl-2-oxoimidazolidin-1-yl)-N-phenylbenzenesulfonamides selectively bioactivated by cytochrome p450 1A1 in breast cancer cells. Cancer Res 1 July 2021; 81 (13_Supplement): 284. https://doi.org/10.1158/1538-7445.AM2021-284
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Chahrazed Bouzriba, Atziri Corin Chavez Alvarez, Mathieu Gagné-Boulet, Jacques Lacroix, Marie-France Côté, René C.-Gaudrault, Sébastien Fortin; Abstract 285: Development of phenyl 4-(2-oxo-3-alkylimidazolidin-1-yl)benzenesulfonates as new antimitotic cytochrome P450 1A1-activated prodrugs selective toward breast cancers: Evaluation of branched alkyl chains. Cancer Res 1 July 2021; 81 (13_Supplement): 285. https://doi.org/10.1158/1538-7445.AM2021-285
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Atziri Corin Chavez Alvarez, Chahrazed Bouzriba, Mathieu Gagné-Boulet, Sylvie Pilote, René C.-Gaudreault, Chantale Simard, Sébastien Fortin; Abstract 1359: Evaluation of the therapeutic potential of AIMZ-938 as a new cytochrome p450 1A1-selective prodrug for the treatment of breast cancers. Cancer Res 1 July 2021; 81 (13_Supplement): 1359. https://doi.org/10.1158/1538-7445.AM2021-1359
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Mathieu Gagné-Boulet, Chahrazed Bouzriba, Atziri Corin Chavez Alvarez, Sébastien Fortin; Abstract 286: Conception and preparation of new potent antimicrotubule agents. Cancer Res 1 July 2021; 81 (13_Supplement): 286. https://doi.org/10.1158/1538-7445.AM2021-286
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Mitra Zarifi Khosroshahi, Atziri Corin Chavez Alvarez, Mathieu Gagné-Boulet, René C.-Gaudreault, Stéphane Gobeil, Sébastien Fortin, Evaluation of the time-dependent antiproliferative activity and liver microsome stability of 3 phenyl 4-(2-oxo-3-alkylimidazolidin-1-yl)benzenesulfonates as promising CYP1A1-dependent antimicrotubule prodrugs, Journal of Pharmacy and Pharmacology, Volume 72, Issue 2, February 2020, Pages 249–258, https://doi.org/10.1111/jphp.13198
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V. Denavit, D. Lainé, C. Bouzriba, E. Shanina, É. Gillon, S. Fortin, C. Rademacher, A. Imberty, D. Giguère, Stereoselective Synthesis of Fluorinated Galactopyranosides as Potential Molecular Probes for Galactophilic Proteins: Assessment of Monofluorogalactoside–LecA Interactions. Chem. Eur. J. 2019, 25, 4478.
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Couillard-Montminy V, Gagnon P-Y, Fortin S, Côté J. Effectiveness of adjuvant carboplatin-based chemotherapy compared to cisplatin in non-small cell lung cancer. Journal of Oncology Pharmacy Practice. 2017;25(1):44-51. doi:10.1177/1078155217724595
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P. M. Vadhadiya, M.-A. Jean, C. Bouzriba, T. Tremblay, P. Lagüe, S. Fortin, J. Boukouvalas, D. Giguère, Diversity-Oriented Synthesis of Diol-Based Peptidomimetics as Potential HIV Protease Inhibitors and Antitumor AgentsChemBioChem 2018, 19, 1779.
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Pauty, J., Côté, MF., Rodrigue, A. et al. Investigation of the DNA damage response to SFOM-0046, a new small-molecule drug inducing DNA double-strand breaks. Sci Rep 6, 23302 (2016). https://doi.org/10.1038/srep23302
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Mathieu Gagné-Boulet, Sébastien Fortin, Jacques Lacroix, Carole-Anne Lefebvre, Marie-France Côté, René C-Gaudreault; Abstract 1664: New moieties mimicking the trimethoxyphenyl (ring A) of combretastatin A-4: Synthesis and biological evaluation. Cancer Res 1 August 2015; 75 (15_Supplement): 1664. https://doi.org/10.1158/1538-7445.AM2015-1664
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Gagné-Boulet M., Fortin S., Lacroix J., Lefebvre C.-A., Côté M.-F. et C.-Gaudreault R. (2015), Styryl-N-phenyl-N'-(2-chloroethyl)ureas and styrylphenylimidazolidin-2-ones as new potent microtubule-disrupting agents using combretastatin A-4 as model, European Journal of Medicinal Chemistry, 100, 34-43.
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Fortin S., Wei L., P. Kotra L. and C.-Gaudreault R. (2015), Novel cytocidal substituted phenyl 4-(2-oxoimidazolidin-1-yl)benzenesulfonates and benzenesulfonamides with affinity to the colchicine-binding site: is the phenyl 2-imidazolidinone moiety a new haptophore for the design of new antimitotics?, Open Journal of Medicinal Chemistry, 5, 9-22.
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Morin N., Bruneau J., Fortin S., Brasseur K., Leblanc V., Asselin É. and Bérubé G. (2015), New testosterone derivatives as semi-synthetic anticancer agents against prostate cancer: synthesis and preliminary biological evaluation, Medicinal Chemistry, 11, 1-9.
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Fortin S., Brasseur K., Morin N., Asselin É. and Bérubé G. (2013), New platinum(II) complexes conjugate at position 7α of 17β-acetyl-testosterone as new combi-molecules against prostate cancer: Design, synthesis, structure-activity relationships and biological evaluation, European Journal of Medicinal Chemistry, 68, 433-443.
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Marceau F., Bouthillier J., Houle S., Sabourin T., Fortin J.-P., Morissette G., Lodge R., Fortin S., C.-Gaudreault R., Bawolak M.-T., Koumbadinga G. A., Roy C., Charest-Morin X. and Gera L. (2013), Bradykinin receptors: agonists, antagonists, expression, signaling and adaptation to sustained stimulation, Journal of Angioedema, 1, 9-17.
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Charest-Morin X., Fortin S., Lodge R., Roy C., Gera L., C.-Gaudreault R. and Marceau F. (2013), Inhibitory effects of cytoskeleton disrupting drugs and GDP-locked Rab mutants on bradykinin B2 receptor cycling, Pharmacological Research, 71, 44-52.
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Saha P., Fortin S., Leblanc V., Asselin É. and Bérubé G. (2012), Design, synthesis, cytocidal activity and estrogen receptor α affinity of doxorubicin conjugates at 16α-position of estrogen for site-specific treatment of estrogen receptor-positive breast cancers, Steroids, 77, 1113-1122.
Profile Details
https://www.pha.ulaval.ca/faculte/repertoire-du-personnel/sebastien-fortin