Kappa opioid antagonists: Past successes and future prospects

被引:84
作者
Metcalf, MD [1 ]
Coop, A [1 ]
机构
[1] Univ Maryland, Sch Pharm, Dept Pharmaceut Sci, Baltimore, MD 21201 USA
关键词
opioid; opiate; receptor; kappa; antagonist;
D O I
10.1208/aapsj070371
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Antagonists of the kappa opioid receptor were initially investigated as pharmacological tools that would reverse the effects of kappa opioid receptor agonists. In the years following the discovery of the first selective kappa opioid antagonists, much information about their chemistry and pharmacology has been elicited and their potential therapeutic uses have been investigated. The review presents the current chemistry, ligand-based structure activity relationships, and pharmacology of the known nonpeptidic selective kappa opioid receptor antagonists. This manuscript endeavors to provide the reader with a useful reference of the investigations made to define the structure-activity relationships and pharmacology of selective kappa opioid receptor antagonists and their potential uses as pharmacological tools and as therapeutic agents in the treatment of disease states.
引用
收藏
页码:E704 / E722
页数:19
相关论文
共 114 条
[1]  
Aldrich J. V., 2003, BURGERS MED CHEM DRU, P329, DOI DOI 10.1002/0471266949.BMC100
[2]   Synthesis, opioid receptor binding, and functional activity of 5′-substituted 17-cyclopropylmethylpyrido[2′,3′:6,7]morphinans [J].
Ananthan, S ;
Kezar, HS ;
Saini, SK ;
Khare, NK ;
Davis, P ;
Dersch, CM ;
Porreca, F ;
Rothman, RB .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2003, 13 (03) :529-532
[3]  
[Anonymous], BUPRENORPHINE COMBAT
[4]  
[Anonymous], 1986, OPIOID ANALGESICS
[5]   Functional effects of systemically administered agonists and antagonists of μ, δ, and κ opioid receptor subtypes on body temperature in mice [J].
Baker, AK ;
Meert, TF .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2002, 302 (03) :1253-1264
[6]   Identification of arodyn, a novel acetylated dynorphin A-(1-11) analogue, as a κ opioid receptor antagonist [J].
Bennett, MA ;
Murray, TF ;
Aldrich, JV .
JOURNAL OF MEDICINAL CHEMISTRY, 2002, 45 (26) :5617-5619
[7]   Non-selective opioid receptor antagonism of the antidepressant-like effect of venlafaxine in the forced swimming test in mice [J].
Berrocoso, E ;
Rojas-Corrales, MO ;
Micó, JA .
NEUROSCIENCE LETTERS, 2004, 363 (01) :25-28
[8]  
BERTALMIO AJ, 1987, J PHARMACOL EXP THER, V243, P591
[9]   Guanidino N-substituted and N,N-disubstituted derivatives of the κ-opioid antagonist GNTI [J].
Black, SL ;
Chauvignac, C ;
Grundt, P ;
Miller, CN ;
Wood, S ;
Traynor, JR ;
Lewis, JW ;
Husbands, SM .
JOURNAL OF MEDICINAL CHEMISTRY, 2003, 46 (25) :5505-5511
[10]   The role of the side chain in determining relative δ- and κ-affinity in C5′-substituted analogues of naltrindole [J].
Black, SL ;
Jales, AR ;
Brandt, W ;
Lewis, JW ;
Husbands, SM .
JOURNAL OF MEDICINAL CHEMISTRY, 2003, 46 (02) :314-317