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European Journal of Medicinal Chemistry
|
January 12, 2018
Novel donepezil-like N-benzylpyridinium salt derivatives as AChE inhibitors and their corresponding dihydropyridine "bio-oxidizable" prodrugs: Synthesis, biological evaluation and structure-activity relationship
Rabah Azzouz, Ludovic Peauger, Vincent Gembus, et al.
The Journal of Organic Chemistry
|
July 14, 2018
Access to Highly Enantioenriched Donepezil-like 1,4-Dihydropyridines as Promising Anti-Alzheimer Prodrug Candidates via Enantioselective Tsuji Allylation and Organocatalytic Aza-Ene-Type Domino Reactions
Mihaela-Liliana Ţînţaş, Rabah Azzouz, Ludovic Peauger, et al.
Journal of Medicinal Chemistry
|
June 15, 2017
Donepezil-Based Central Acetylcholinesterase Inhibitors by Means of a "Bio-Oxidizable" Prodrug Strategy: Design, Synthesis, and in Vitro Biological Evaluation
Ludovic Peauger, Rabah Azzouz, Vincent Gembus, et al.
RSC Medicinal Chemistry
|
March 22, 2024
Design, synthesis and preliminary biological evaluation of rivastigmine-INDY hybrids as multitarget ligands against Alzheimer's disease by targeting butyrylcholinesterase and DYRK1A/CLK1 kinases
Mihaela-Liliana Ţînţaş, Ludovic Peauger, Anaïs Barré, et al.
European Journal of Medicinal Chemistry
|
June 11, 2018
Rational design of carbamate-based dual binding site and central AChE inhibitors by a "biooxidisable" prodrug approach: Synthesis, in vitro evaluation and docking studies
Mihaela-Liliana Ţînţaş, Vincent Gembus, Florent Alix, et al.
Molecules (Basel, Switzerland)
|
January 8, 2023
Straightforward Access to a New Class of Dual DYRK1A/CLK1 Inhibitors Possessing a Simple Dihydroquinoline Core
Mihaela-Liliana Ţînţaş, Ludovic Peauger, Florent Alix, et al.
ACS Chemical Neuroscience
|
February 20, 2015
Dihydroquinoline Carbamate Derivatives as "Bio-oxidizable" Prodrugs for Brain Delivery of Acetylcholinesterase Inhibitors: [¹¹C] Radiosynthesis and Biological Evaluation
Pierre Bohn, Fabienne Gourand, Cyril Papamicaël, et al.
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Showing results (11-20 of 17) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 17 results.
European Journal of Medicinal Chemistry
|
January 12, 2018
Novel donepezil-like N-benzylpyridinium salt derivatives as AChE inhibitors and their corresponding dihydropyridine "bio-oxidizable" prodrugs: Synthesis, biological evaluation and structure-activity relationship
Rabah Azzouz, Ludovic Peauger, Vincent Gembus, et al.
The Journal of Organic Chemistry
|
July 14, 2018
Access to Highly Enantioenriched Donepezil-like 1,4-Dihydropyridines as Promising Anti-Alzheimer Prodrug Candidates via Enantioselective Tsuji Allylation and Organocatalytic Aza-Ene-Type Domino Reactions
Mihaela-Liliana Ţînţaş, Rabah Azzouz, Ludovic Peauger, et al.
Journal of Medicinal Chemistry
|
June 15, 2017
Donepezil-Based Central Acetylcholinesterase Inhibitors by Means of a "Bio-Oxidizable" Prodrug Strategy: Design, Synthesis, and in Vitro Biological Evaluation
Ludovic Peauger, Rabah Azzouz, Vincent Gembus, et al.
RSC Medicinal Chemistry
|
March 22, 2024
Design, synthesis and preliminary biological evaluation of rivastigmine-INDY hybrids as multitarget ligands against Alzheimer's disease by targeting butyrylcholinesterase and DYRK1A/CLK1 kinases
Mihaela-Liliana Ţînţaş, Ludovic Peauger, Anaïs Barré, et al.
European Journal of Medicinal Chemistry
|
June 11, 2018
Rational design of carbamate-based dual binding site and central AChE inhibitors by a "biooxidisable" prodrug approach: Synthesis, in vitro evaluation and docking studies
Mihaela-Liliana Ţînţaş, Vincent Gembus, Florent Alix, et al.
Molecules (Basel, Switzerland)
|
January 8, 2023
Straightforward Access to a New Class of Dual DYRK1A/CLK1 Inhibitors Possessing a Simple Dihydroquinoline Core
Mihaela-Liliana Ţînţaş, Ludovic Peauger, Florent Alix, et al.
ACS Chemical Neuroscience
|
February 20, 2015
Dihydroquinoline Carbamate Derivatives as "Bio-oxidizable" Prodrugs for Brain Delivery of Acetylcholinesterase Inhibitors: [¹¹C] Radiosynthesis and Biological Evaluation
Pierre Bohn, Fabienne Gourand, Cyril Papamicaël, et al.
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of 2