Investigation of the Selectivity of Oxymorphone- and Naltrexone-Derived Ligands via Site-Directed Mutagenesis of Opioid Receptors: Exploring the ‘Address' Recognition Locus
- 15 February 2001
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of Medicinal Chemistry
- Vol. 44 (6) , 857-862
- https://doi.org/10.1021/jm000381r
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- An alpha-carbon template for the transmembrane helices in the rhodopsin family of G-protein-coupled receptors 1 1Edited by R. HuberJournal of Molecular Biology, 1997
- Pyrrolomorphinans as δ Opioid Receptor Antagonists. The Role of Steric Hindrance in Conferring SelectivityJournal of Medicinal Chemistry, 1997
- Application of the message-address concept to the docking of naltrexone and selective naltrexone-derived opioid antagonists into opioid receptor modelsNeurochemical Research, 1996
- On the role of extracellular loops of opioid receptors in conferring ligand selectivityFEBS Letters, 1995
- Cloning and pharmacological characterization of a rat μ opioid receptorNeuron, 1993
- Cloning and functional comparison of kappa and delta opioid receptors from mouse brain.Proceedings of the National Academy of Sciences, 1993
- Cloning of a Delta Opioid Receptor by Functional ExpressionScience, 1992
- Selective Natrexone-Derived Opioid Receptor AntagonistsAnnual Review of Pharmacology and Toxicology, 1992
- ACTH: A SHORT INTRODUCTORY REVIEW*Annals of the New York Academy of Sciences, 1977
- A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye bindingAnalytical Biochemistry, 1976