Preclinical Disposition (In Vitro) of Novel μ-Opioid Receptor Selective Antagonists-Reference-Cited by-同舟云学术

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Preclinical Disposition (In Vitro) of Novel μ-Opioid Receptor Selective Antagonists

Published:2011-06-17 Issue:9 Volume:39 Page:1589-1596
ISSN:0090-9556
Container-title:Drug Metabolism and Disposition
language:en
Short-container-title:Drug Metab Dispos

Author:

Mitra Pallabi,Venitz Jürgen,Yuan Yunyun,Zhang Yan,Gerk Phillip M.

Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

Subject

Pharmaceutical Science,Pharmacology

Reference35 articles.

1. Bidlack JM Mathews JL (2009) The chemistry and pharmacology of μ-opioid receptors, in Opiate Receptors and Antagonists—From Bench to Clinic ( Dean R Bilsky EJ Negus SS eds) pp 83–97, Humana Press, New York.

2. Carbonyl reduction of naltrexone and dolasetron by oxidoreductases isolated from human liver cytosol

3. Microsomal codeine N-demethylation: cosegregation with cytochrome P4503A4 activity;Caraco;Drug Metab Dispos,1996

4. Copeland RA (2000) Enzymes: A Practical Introduction to Structure, Mechanism, and Data Analysis, John Wiley & Sons, New York.

5. Regional levels of drug transporters along the human intestinal tract: Co-expression of ABC and SLC transporters and comparison with Caco-2 cells

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