Alix F

Title : Rational design of carbamate-based dual binding site and central AChE inhibitors by a 'biooxidisable' prodrug approach: Synthesis, invitro evaluation and docking studies - Tintas_2018_Eur.J.Med.Chem_155_171

Author(s) : Tintas ML , Gembus V , Alix F , Barre A , Coadou G , Truong L , Sebban M , Papamical C , Oulyadi H , Levacher V

Ref : Eur Journal of Medicinal Chemistry , 155 :171 , 2018

Abstract : Tintas_2018_Eur.J.Med.Chem_155_171

ESTHER : Tintas_2018_Eur.J.Med.Chem_155_171

PubMedSearch : Tintas_2018_Eur.J.Med.Chem_155_171

PubMedID: 29886321

Title : Dihydroquinoline Carbamate Derivatives as Bio-oxidizable Prodrugs for Brain Delivery of Acetylcholinesterase Inhibitors: [(11)C] Radiosynthesis and Biological Evaluation - Bohn_2015_ACS.Chem.Neurosci_6_737

Author(s) : Bohn P , Gourand F , Papamicael C , Ibazizene M , Dhilly M , Gembus V , Alix F , Tintas ML , Marsais F , Barre L , Levacher V

Ref : ACS Chem Neurosci , 6 :737 , 2015

Abstract : Bohn_2015_ACS.Chem.Neurosci_6_737

ESTHER : Bohn_2015_ACS.Chem.Neurosci_6_737

PubMedSearch : Bohn_2015_ACS.Chem.Neurosci_6_737

PubMedID: 25695305

Alix F

References (2)

1. Rational design of carbamate-based dual binding site and central AChE inhibitors by a 'biooxidisable' prodrug approach: Synthesis, invitro evaluation and docking studies

2. Dihydroquinoline Carbamate Derivatives as Bio-oxidizable Prodrugs for Brain Delivery of Acetylcholinesterase Inhibitors: [(11)C] Radiosynthesis and Biological Evaluation