5′-guanidinonaltrindole, a highly selective and potent κ-opioid receptor antagonist

被引:79
作者
Jones, RM [1 ]
Portoghese, PS [1 ]
机构
[1] Univ Minnesota, Coll Pharm, Dept Med Chem, Minneapolis, MN 55455 USA
关键词
norbinaltorphimine; binding; kappa-opioid receptor;
D O I
10.1016/S0014-2999(00)00208-9
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
5'-Guanidinonaltrindole (GNTI) possesses 5-fold greater opioid antagonist potency (K-e = 0.04 nM) and an order of magnitude greater selectivity (selectivity ratios > 500) than the prototypical kappa-opioid receptor antagonist, norbinaltorphimine, in smooth muscle preparations. Binding and functional studies conducted on cloned human opioid receptors expressed in Chinese hamster ovarian (CHO) cells afforded pA(2) values that were comparable to the smooth muscle data. In view of the high selectivity and potency of GNTI, it is a potentially valuable pharmacological tool for opioid research. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:49 / 52
页数:4
相关论文
共 12 条
[1]   [S-35]GTP gamma S binding: A tool to evaluate functional activity of a cloned opioid receptor transiently expressed in COS cells [J].
Befort, K ;
Tabbara, L ;
Kieffer, BL .
NEUROCHEMICAL RESEARCH, 1996, 21 (11) :1301-1307
[2]  
CHENG Y, 1973, BIOCHEM PHARMACOL, V22, P3099
[3]  
Dhawan BN, 1996, PHARMACOL REV, V48, P567
[4]   NEW EXAMPLE OF A MORPHINE-SENSITIVE NEURO-EFFECTOR JUNCTION - ADRENERGIC TRANSMISSION IN MOUSE VAS-DEFERENS [J].
HENDERSON, G ;
HUGHES, J ;
KOSTERLITZ, HW .
BRITISH JOURNAL OF PHARMACOLOGY, 1972, 46 (04) :764-766
[5]  
HJORTH SA, 1995, MOL PHARMACOL, V47, P1089
[6]   Mutational evidence for a common κ antagonist binding pocket in the wild-type κ and mutant μ[K303E] opioid receptors [J].
Jones, RM ;
Hjorth, SA ;
Schwartz, TW ;
Portoghese, PS .
JOURNAL OF MEDICINAL CHEMISTRY, 1998, 41 (25) :4911-4914
[7]   A REMARKABLE CHANGE OF OPIOID RECEPTOR SELECTIVITY ON THE ATTACHMENT OF A PEPTIDOMIMETIC KAPPA ADDRESS ELEMENT TO THE DELTA ANTAGONIST, NATRINDOLE - 5'-[(N-2-ALKYLAMIDINO)METHYL]NALTRINDOLE DERIVATIVES AS A NOVEL CLASS OF KAPPA OPIOID RECEPTOR ANTAGONISTS [J].
OLMSTED, SL ;
TAKEMORI, AE ;
PORTOGHESE, PS .
JOURNAL OF MEDICINAL CHEMISTRY, 1993, 36 (01) :179-180
[8]  
Paterlini G, 1997, J MED CHEM, V40, P3254
[9]   DESIGN OF PEPTIDOMIMETIC DELTA-OPIOID RECEPTOR ANTAGONISTS USING THE MESSAGE ADDRESS CONCEPT [J].
PORTOGHESE, PS ;
SULTANA, M ;
TAKEMORI, AE .
JOURNAL OF MEDICINAL CHEMISTRY, 1990, 33 (06) :1714-1720
[10]   STIMULANT ACTIONS OF VOLATILE ANAESTHETICS ON SMOOTH MUSCLE [J].
RANG, HP .
BRITISH JOURNAL OF PHARMACOLOGY AND CHEMOTHERAPY, 1964, 22 (02) :356-&