New structure–activity relationship studies in a series of N,N-bis(cyclohexanol)amine aryl esters as potent reversers of P-glycoprotein-mediated multidrug resistance (MDR)-Reference-Cited by-同舟云学术

New structure–activity relationship studies in a series of N,N-bis(cyclohexanol)amine aryl esters as potent reversers of P-glycoprotein-mediated multidrug resistance (MDR)

Published:2013-01 Issue:2 Volume:21 Page:456-465
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Orlandi Francesca,Coronnello Marcella,Bellucci Cristina,Dei Silvia,Guandalini Luca,Manetti Dina,Martelli Cecilia,Romanelli Maria Novella,Scapecchi Serena,Salerno Milena,Menif Hayette,Bello Ivan,Mini Enrico,Teodori Elisabetta

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference50 articles.

1. Structure of Multidrug-Resistance Proteins of the ATP-Binding Cassette (ABC) Superfamily

2. MDR1-P-Glycoprotein (ABCB1) Mediates Transport of Alzheimer’s Amyloid-β Peptides—Implications for the Mechanisms of Aβ Clearance at the Blood–Brain Barrier

3. Multiple physiological functions for multidrug transporter P-glycoprotein?

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