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Jenny Roy
Observed name:
Roy Jenny
Institutions:
Centre hospitalier de l'Université Laval,
Université Laval,
Centre de recherche du CHU de Québec-Université Laval
Observed institutions:
Centre hospitalier universitaire de Québec,
Centre hospitalier de l'Université Laval,
Université Laval,
Quebec Research and Development Centre,
Centre de recherche du CHU de Québec-Université Laval,
CHU de Québec-Université Laval
show all 6
ORCID:
0000-0002-9928-3009
Observed ORCID:
0000-0002-9928-3009
OpenAlex ID:
A5102962545
Impact of estradiol structural modifications (18-methyl and/or 17-hydroxy inversion of configuration) on the in vitro and in vivo estrogenic activity
2011
·
Diana Ayan
, Jenny Roy
, et al.
·
The Journal of Steroid Biochemistry and Molecular Biology
·
58
In vitro antileukemia, antibacterial and antifungal activities of some 3d metal complexes: Chemical synthesis and structure – activity relationships
2008
·
Aurelian Gulea
, Donald Poirier
, et al.
·
Journal of Enzyme Inhibition and Medicinal Chemistry
·
53
PDF
A New Nonestrogenic Steroidal Inhibitor of 17β-Hydroxysteroid Dehydrogenase Type I Blocks the Estrogen-Dependent Breast Cancer Tumor Growth Induced by Estrone
2012
·
Diana Ayan
, René Maltais
, et al.
·
Molecular Cancer Therapeutics
·
44
2β-(N-Substituted Piperazino)-5α-Androstane-3α,17β-Diols: Parallel Solid-Phase Synthesis and Antiproliferative Activity on Human Leukemia HL-60 Cells
2007
·
Jenny Roy
, Patrick DeRoy
, et al.
·
Journal of Combinatorial Chemistry
·
40
Copper(II) and uranyl(II) complexes with acylthiosemicarbazide: Synthesis, characterization, antibacterial activity and effects on the growth of promyelocytic leukemia cells HL-60
2009
·
Madalina Veronica Angelusiu
, Gabriela Laura Almajan
, et al.
·
European Journal of Medicinal Chemistry
·
39
Comparison of the effects of EM‐652 (SCH57068), tamoxifen, toremifene, droloxifene, idoxifene, GW‐5638 and raloxifene on the growth of human ZR‐75‐1 breast tumors in nude mice
2002
·
Matthieu Gutman
, Steeve Couillard
, et al.
·
International Journal of Cancer
·
37
Targeting Cytochrome P450 (CYP) 1B1 Enzyme with Four Series of A-Ring Substituted Estrane Derivatives: Design, Synthesis, Inhibitory Activity, and Selectivity
2018
·
Raphaël Dutour
, Jenny Roy
, et al.
·
Journal of Medicinal Chemistry
·
35
Design of a Mestranol 2‐N‐Piperazino‐Substituted Derivative Showing Potent and Selective in vitro and in vivo Activities in MCF‐7 Breast Cancer Models
2017
·
Martin Perreault
, René Maltais
, et al.
·
ChemMedChem
·
30
PDF
Turning a Quinoline-based Steroidal Anticancer Agent into Fluorescent Dye for its Tracking by Cell Imaging
2021
·
René Maltais
, Jenny Roy
, et al.
·
ACS Medicinal Chemistry Letters
·
29
A novel aminosteroid of the 5α-androstane-3α,17β-diol family induces cell cycle arrest and apoptosis in human promyelocytic leukemia HL-60 cells
2010
·
Hajer Jegham
, Jenny Roy
, et al.
·
Investigational New Drugs
·
28
Chemical synthesis, NMR analysis and evaluation on a cancer xenograft model (HL-60) of the aminosteroid derivative RM-133
2014
·
René Maltais
, Audrey Delhomme
, et al.
·
Steroids
·
27
Chemical synthesis of 2β-amino-5α-androstane-3α,17β-diol N-derivatives and their antiproliferative effect on HL-60 human leukemia cells
2008
·
Dominic Thibeault
, Jenny Roy
, et al.
·
Bioorganic & Medicinal Chemistry
·
27
Libraries of 2β-(N-substituted piperazino)-5α-androstane-3α, 17β-diols: chemical synthesis and cytotoxic effects on human leukemia HL-60 cells and on normal lymphocytes
2010
·
Jenny Roy
, René Maltais
, et al.
·
Molecular Diversity
·
26
A Targeted-Covalent Inhibitor of 17β-HSD1 Blocks Two Estrogen-Biosynthesis Pathways: In Vitro (Metabolism) and In Vivo (Xenograft) Studies in T-47D Breast Cancer Models
2021
·
Donald Poirier
, Jenny Roy
, et al.
·
Cancers
·
22
PDF
Identification of steroidal derivatives inhibiting the transformations of allopregnanolone and estradiol by 17β-hydroxysteroid dehydrogenase type 10
2018
·
Sophie Boutin
, Jenny Roy
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
21
The Aminosteroid Derivative RM-133 Shows In Vitro and In Vivo Antitumor Activity in Human Ovarian and Pancreatic Cancers
2015
·
Lucie Carolle Kenmogne
, Diana Ayan
, et al.
·
PLoS ONE
·
21
PDF
Inhibition of dehydroepiandosterone sulfate action in androgen-sensitive tissues by EM-1913, an inhibitor of steroid sulfatase
2013
·
Jenny Roy
, Julie Lefebvre
, et al.
·
Molecular and Cellular Endocrinology
·
20
Synthesis of 17β-hydroxysteroid dehydrogenase type 10 steroidal inhibitors: Selectivity, metabolic stability and enhanced potency
2020
·
Sophie Boutin
, René Maltais
, et al.
·
European Journal of Medicinal Chemistry
·
19
Induction of endoplasmic reticulum stress by aminosteroid derivative RM-581 leads to tumor regression in PANC-1 xenograft model
2018
·
Martin Perreault
, René Maltais
, et al.
·
Investigational New Drugs
·
19
Structure-Based Design and Synthesis of New Estrane–Pyridine Derivatives as Cytochrome P450 (CYP) 1B1 Inhibitors
2017
·
Raphaël Dutour
, Francisco Cortés-Benítez
, et al.
·
ACS Medicinal Chemistry Letters
·
19
A Novel Pure SERM Achieves Complete Regression of the Majority of Human Breast Cancer Tumors in Nude Mice
2003
·
Jenny Roy
, Steeve Couillard
, et al.
·
Breast Cancer Research and Treatment
·
19
Pharmacokinetic profile of PBRM in rodents, a first selective covalent inhibitor of 17β-HSD1 for breast cancer and endometriosis treatments
2017
·
René Maltais
, Alexandre Trottier
, et al.
·
The Journal of Steroid Biochemistry and Molecular Biology
·
18
Design, chemical synthesis and biological evaluation of 3-spiromorpholinone/3-spirocarbamate androsterone derivatives as inhibitors of 17β-hydroxysteroid dehydrogenase type 3
2015
·
Guy Bertrand Djigoué
, Lucie Carolle Kenmogne
, et al.
·
Bioorganic & Medicinal Chemistry
·
18
An irreversible inhibitor of 17β-hydroxysteroid dehydrogenase type 1 inhibits estradiol synthesis in human endometriosis lesions and induces regression of the non-human primate endometriosis
2022
·
Donald Poirier
, Atunga Nyachieo
, et al.
·
The Journal of Steroid Biochemistry and Molecular Biology
·
17
Biological evaluation of a new family of aminosteroids that display a selective toxicity for various malignant cell lines
2012
·
Hajer Jegham
, René Maltais
, et al.
·
Anti-Cancer Drugs
·
17
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Works count:
78
Citation count:
987
H-index:
19
I10-index:
41
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