Kappa opioid antagonists have the potential to be developed as a pharmacotherapy for cocaine abuse. Antagonists of the kappa receptor system are needed to fully study the kappa opioid receptor system to develop a pharmacotherapy for cocaine abuse. Kappa opioid antagonists are both few in number and have associated problems with onset and a long duration of action. The goal of this research is to develop novel kappa opioid antagonists with excellent kappa opioid antagonist activity that also have a shortened duration of action. The approach to be used consists of developing kappa antagonists with metabolically labile groups which will produce the desired shortened duration of action. The current hypothesis is that the labile group attached to a kappa antagonist, once metabolized, will produce a compound which has no opioid activity. Thus, the parent compound will have kappa opioid antagonist activity and the metabolite will be devoid of kappa opioid activity. The duration of action will then depend strictly upon the rate metabolism leading to a shortened duration of action kappa antagonist.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
1F31DA018025-01A1
Application #
6885193
Study Section
Human Development Research Subcommittee (NIDA)
Program Officer
Lawrence, Diane M
Project Start
2005-05-01
Project End
2007-04-30
Budget Start
2005-05-01
Budget End
2006-04-30
Support Year
1
Fiscal Year
2005
Total Cost
$26,522
Indirect Cost
Name
University of Maryland Baltimore
Department
Pharmacology
Type
Schools of Pharmacy
DUNS #
188435911
City
Baltimore
State
MD
Country
United States
Zip Code
21201
Metcalf, Matthew D; Rosicky, Andrew D; Hassan, Hazem E et al. (2014) Opioids and efflux transporters. Part 4: influence of N-substitution on P-glycoprotein substrate activity of noroxymorphone analogues. Bioorg Med Chem Lett 24:3592-5
Metcalf, Matthew D; Aceto, Mario D; Harris, Louis S et al. (2008) The influence of esters and carboxylic acids as the N-substituent of opioids. Part 1: Benzomorphans. Bioorg Med Chem 16:869-73
Metcalf, Matthew D; Coop, Andrew (2007) 5'-halogenated analogs of oxymorphindole. Bioorg Med Chem Lett 17:5916-7