Drug Rescue Distinguishes between Different Structural Models of Human P-Glycoprotein
Author:
Affiliation:
1. Departments of Medicine and Biochemistry, University of Toronto, Toronto, Ontario M5S 1A8, Canada
Publisher
American Chemical Society (ACS)
Subject
Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/bi401269m
Reference21 articles.
1. Shedding light on drug transport: structure and function of the P-glycoprotein multidrug transporter (ABCB1)This paper is one of a selection of papers published in this Special Issue, entitled CSBMCB — Membrane Proteins in Health and Disease.
2. BIOCHEMICAL, CELLULAR, AND PHARMACOLOGICAL ASPECTS OF THE MULTIDRUG TRANSPORTER
3. ABC Efflux Pump-Based Resistance to Chemotherapy Drugs
4. Comparison of the inward- and outward-open homology models and ligand binding of human P-glycoprotein
5. Exhaustive Sampling of Docking Poses Reveals Binding Hypotheses for Propafenone Type Inhibitors of P-Glycoprotein
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1. A review on dynamics of permeability-glycoprotein in efflux of chemotherapeutic drugs;Frontiers in Drug Discovery;2024-04-11
2. Targeting P-glycoprotein: Investigation of piperine analogs for overcoming drug resistance in cancer;Scientific Reports;2017-08-11
3. Folding correction of ABC-transporter ABCB1 by pharmacological chaperones: a mechanistic concept;Pharmacology Research & Perspectives;2017-05-26
4. About P‐glycoprotein: a new drugable domain is emerging from structural data;WIREs Computational Molecular Science;2017-05-04
5. The therapeutic potential of targeting ABC transporters to combat multi-drug resistance;Expert Opinion on Therapeutic Targets;2017-04-03
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