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4,4-Dimethyl-1,2,3,4-tetrahydroquinline-based PPARΑ/Γ agonists. Part I: Synthesis and pharmacological evaluation

Bioorganic & medicinal chemistry letters, 2008, Vol.18

2008

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4,4-Dimethyl-1,2,3,4-tetrahydroquinoline-based PPARalpha/gamma agonists. Part I: synthesis and pharmacological evaluation

Bioorganic & medicinal chemistry letters, 2008-03, Vol.18 (5), p.1617-1622

2008

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4,4-Dimethyl-1,2,3,4-tetrahydroquinoline-based PPARalpha/gamma agonists. Part. II: Synthesis and pharmacological evaluation of oxime and acidic head group structural variations

Bioorganic & medicinal chemistry letters, 2009-05, Vol.19 (10), p.2683-2687

2009

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4,4-Dimethyl-1,2,3,4-tetrahydroquinoline-based PPARα/γ agonists. Part I: Synthesis and pharmacological evaluation

Bioorganic & medicinal chemistry, 2008-03, Vol.18 (5), p.1617-1622

2008

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4,4-Dimethyl-1,2,3,4-tetrahydroquinoline-based PPARα/γ agonists. Part. II: Synthesis and pharmacological evaluation of oxime and acidic head group structural variations

Bioorganic & medicinal chemistry letters, 2009-05, Vol.19 (10), p.2683-2687

2009

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Abstract 4115: ADCs optimization lead to a significant anti-tumoral activity in lymphoma and breast tumor xenograft mouse models

Cancer research (Chicago, Ill.), 2020-08, Vol.80 (16_Supplement), p.4115-4115

2020

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Adcitmer®, a new CD56‐targeting monomethyl auristatin E‐conjugated antibody, is a potential therapeutic approach in Merkel cell carcinoma

British journal of dermatology (1951), 2022-02, Vol.186 (2), p.295-306

2022

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L’Adcitmer, un nouvel anticorps ciblant le CD56, bioconjugé à la MMAE, comme perspective thérapeutique dans le carcinome de Merkel

Annales de dermatologie et de vénéréologie, 2020-12, Vol.147 (12), p.A92-A93

2020

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α-Lithiation and electrophilic substitution of 1,4,4-trimethyl-3,4-dihydroquinolin-2-one

Molecules (Basel, Switzerland), 2010-10, Vol.15 (11), p.7742-7749

2010

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[alpha]-Lithiation and Electrophilic Substitution of 1,4,4-Trimethyl-3,4-dihydroquinolin-2-one

Molecules (Basel, Switzerland), 2010-11, Vol.15 (11), p.7742

2010

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AmpD is required for regulation of expression of NmcA, a carbapenem-hydrolyzing β-lactamase of Enterobacter cloacae

Antimicrobial agents and chemotherapy, 2001-10, Vol.45 (10), p.2908-2915

2001

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AmpD Is Required for Regulation of Expression of NmcA, a Carbapenem-Hydrolyzing β-Lactamase ofEnterobacter cloacae

Antimicrobial Agents and Chemotherapy, 2001-10, Vol.45 (10), p.2908-2915

2001

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Analyse d’une infrastructure québécoise de transfert de connaissances en autisme : le RNETSA

Santé publique (Vandoeuvre-lès-Nancy, France), 2024-06, Vol.36 (3), p.21-31

2024

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Antibody-Drug Conjugates as an Emerging Therapy in Oncodermatology

Cancers, 2022-02, Vol.14 (3), p.778

2022

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Antibody-drug conjugates: Design and development for therapy and imaging in and beyond cancer, LabEx MAbImprove industrial workshop, July 27-28, 2017, Tours, France

mAbs, 2018-02, Vol.10 (2), p.210-221

2018

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Antibody-drug conjugates: Design and development for therapy and imaging in and beyond cancer, LabEx MAbImprove industrial workshop, July 27-28, 2017, Tours, France

mAbs, 2018, Vol.10 (2), p.210-221

2018

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Anticalin N- or C-Terminal on a Monoclonal Antibody Affects Both Production and In Vitro Functionality

Antibodies (Basel), 2022-09, Vol.11 (3), p.54

2022

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Characterization of the melatoninergic MT 3 binding site on the NRH:quinone oxidoreductase 2 enzyme

Biochemical pharmacology, 2005, Vol.71 (1), p.74-88

2005

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Characterization of the melatoninergic MT3 binding site on the NRH:quinone oxidoreductase 2 enzyme

Biochemical pharmacology, 2005-12, Vol.71 (1-2), p.74-88

2005

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ChemInform Abstract: A Convenient Synthesis of New Pyrido[3,2-e][1,4]diazepine-2,5-diones and Pyrido[2,3-e][1,4]diazepine-2,5-diones

ChemInform, 2012-01, Vol.43 (3), p.no-no

2012

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ChemInform Abstract: A Novel and Convenient Method for the Synthesis of New Derivatives of Pyrido[3,2-e]pyrrolo[1,2-a][1,4]diazepine-6,11-dione

ChemInform, 2013-03, Vol.44 (13), p.no-no

2013

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ChemInform Abstract: An Efficient and Convenient Method for Synthesizing New Derivatives of Pyrido[2,3-e]pyrrolo[1,2-a][1,4]diazepine-5,10-dione via Sonogashira, Suzuki-Miyaura, and Stille Cross-Coupling Reactions

ChemInform, 2013-03, Vol.44 (12), p.no-no

2013

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ChemInform Abstract: Desulfonylation of Indoles and 7-Azaindoles Using Sodium tert-Butoxide

ChemInform, 2010-10, Vol.41 (43), p.no-no

2010

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ChemInform Abstract: Efficient and General Protocol for Sonogashira Cross-Coupling Reactions of Maleimides

ChemInform, 2012-09, Vol.43 (37), p.no-no

2012

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ChemInform Abstract: Palladium‐Catalyzed Amination of N‐Free 2‐Chloro‐7‐azaindole

ChemInform, 2016-02, Vol.47 (8), p.no-no

2016

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4,4-Dimethyl-1,2,3,4-tetrahydroquinline-based PPARΑ/Γ agonists. Part I: Synthesis and pharmacological evaluation

4,4-Dimethyl-1,2,3,4-tetrahydroquinoline-based PPARalpha/gamma agonists. Part I: synthesis and pharmacological evaluation

4,4-Dimethyl-1,2,3,4-tetrahydroquinoline-based PPARalpha/gamma agonists. Part. II: Synthesis and pharmacological evaluation of oxime and acidic head group structural variations

4,4-Dimethyl-1,2,3,4-tetrahydroquinoline-based PPARα/γ agonists. Part I: Synthesis and pharmacological evaluation

4,4-Dimethyl-1,2,3,4-tetrahydroquinoline-based PPARα/γ agonists. Part. II: Synthesis and pharmacological evaluation of oxime and acidic head group structural variations

Abstract 4115: ADCs optimization lead to a significant anti-tumoral activity in lymphoma and breast tumor xenograft mouse models

Adcitmer®, a new CD56‐targeting monomethyl auristatin E‐conjugated antibody, is a potential therapeutic approach in Merkel cell carcinoma

L’Adcitmer, un nouvel anticorps ciblant le CD56, bioconjugé à la MMAE, comme perspective thérapeutique dans le carcinome de Merkel

α-Lithiation and electrophilic substitution of 1,4,4-trimethyl-3,4-dihydroquinolin-2-one

[alpha]-Lithiation and Electrophilic Substitution of 1,4,4-Trimethyl-3,4-dihydroquinolin-2-one

AmpD is required for regulation of expression of NmcA, a carbapenem-hydrolyzing β-lactamase of Enterobacter cloacae

AmpD Is Required for Regulation of Expression of NmcA, a Carbapenem-Hydrolyzing β-Lactamase ofEnterobacter cloacae

Analyse d’une infrastructure québécoise de transfert de connaissances en autisme : le RNETSA

Antibody-Drug Conjugates as an Emerging Therapy in Oncodermatology

Antibody-drug conjugates: Design and development for therapy and imaging in and beyond cancer, LabEx MAbImprove industrial workshop, July 27-28, 2017, Tours, France

Antibody-drug conjugates: Design and development for therapy and imaging in and beyond cancer, LabEx MAbImprove industrial workshop, July 27-28, 2017, Tours, France

Anticalin N- or C-Terminal on a Monoclonal Antibody Affects Both Production and In Vitro Functionality

Characterization of the melatoninergic MT 3 binding site on the NRH:quinone oxidoreductase 2 enzyme

Characterization of the melatoninergic MT3 binding site on the NRH:quinone oxidoreductase 2 enzyme

ChemInform Abstract: A Convenient Synthesis of New Pyrido[3,2-e][1,4]diazepine-2,5-diones and Pyrido[2,3-e][1,4]diazepine-2,5-diones

ChemInform Abstract: A Novel and Convenient Method for the Synthesis of New Derivatives of Pyrido[3,2-e]pyrrolo[1,2-a][1,4]diazepine-6,11-dione

ChemInform Abstract: An Efficient and Convenient Method for Synthesizing New Derivatives of Pyrido[2,3-e]pyrrolo[1,2-a][1,4]diazepine-5,10-dione via Sonogashira, Suzuki-Miyaura, and Stille Cross-Coupling Reactions

ChemInform Abstract: Desulfonylation of Indoles and 7-Azaindoles Using Sodium tert-Butoxide

ChemInform Abstract: Efficient and General Protocol for Sonogashira Cross-Coupling Reactions of Maleimides

ChemInform Abstract: Palladium‐Catalyzed Amination of N‐Free 2‐Chloro‐7‐azaindole

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