-
2
-
-
3242728388
-
The analgesic effectiveness of nalorphine and nalorphine-morphine combinations in man
-
LASAGNE L, BEECHER H: The analgesic effectiveness of nalorphine and nalorphine-morphine combinations in man. J. Pharmacol. Exp. Ther. (1954) 122:356-363.
-
(1954)
J. Pharmacol. Exp. Ther.
, vol.122
, pp. 356-363
-
-
Lasagne, L.1
Beecher, H.2
-
3
-
-
0014172174
-
Opioid antagonists
-
MARTIN WR: Opioid antagonists. Pharmacol. Rev. (1967) 19:463-521.
-
(1967)
Pharmacol. Rev.
, vol.19
, pp. 463-521
-
-
Martin, W.R.1
-
4
-
-
0013974234
-
Inhibition of writhing by narcotic antagonists
-
PEARL J, HARRIS LS: Inhibition of writhing by narcotic antagonists. J. Pharmacol. Exp. Ther. (1966) 154:319-323.
-
(1966)
J. Pharmacol. Exp. Ther.
, vol.154
, pp. 319-323
-
-
Pearl, J.1
Harris, L.S.2
-
6
-
-
0013832249
-
Studies of the dependence producing potential of the narcotic antagonist 2-cyclopropylmethyl-2′ -hydroxy-5,9-dimethyl-6,7-benzmorphan
-
MARTIN WR, FRASER HF, GORODETZKY CW, ROSENBERG DE: Studies of the dependence producing potential of the narcotic antagonist 2-cyclopropylmethyl-2′-hydroxy-5,9-dimethyl-6,7-benzmorphan. J. Pharmacol. Exp. Ther. (1965) 150:426-436.
-
(1965)
J. Pharmacol. Exp. Ther.
, vol.150
, pp. 426-436
-
-
Martin, W.R.1
Fraser, H.F.2
Gorodetzky, C.W.3
Rosenberg, D.E.4
-
8
-
-
0022494591
-
Psychotomimesis mediated by κ-opiate receptors
-
PFEIFFER A, BRANTL V, HERZ A: Psychotomimesis mediated by κ-opiate receptors. Science (1986) 233:774-776.
-
(1986)
Science
, vol.233
, pp. 774-776
-
-
Pfeiffer, A.1
Brantl, V.2
Herz, A.3
-
9
-
-
0028102960
-
Diuretic effects, pharmacokinetics, and safety of a new centrally acting κ-opioid agonist (CI-977) in humans
-
REECE PA, SEDMAN AJ, ROSE S, WRIGHT DS, DAWKINS R, RAJAGOPALAN R: Diuretic effects, pharmacokinetics, and safety of a new centrally acting κ-opioid agonist (CI-977) in humans. J. Clin. Pharmacol. (1994) 34:1126-1132.
-
(1994)
J. Clin. Pharmacol.
, vol.34
, pp. 1126-1132
-
-
Reece, P.A.1
Sedman, A.J.2
Rose, S.3
Wright, D.S.4
Dawkins, R.5
Rajagopalan, R.6
-
10
-
-
0027215839
-
Neuroendocrine and behavioural effects of the selective κ-agonist spiradoline in Tourette's syndrome: A pilot study
-
CHAPPELL PB, LECKMAN JF, SCAHILL LD, HARDIN MT, ANDERSON G, COHEN DJ: Neuroendocrine and behavioural effects of the selective κ-agonist spiradoline in Tourette's syndrome: a pilot study. Psychiatry Res. (1993) 47:267-280.
-
(1993)
Psychiatry Res.
, vol.47
, pp. 267-280
-
-
Chappell, P.B.1
Leckman, J.F.2
Scahill, L.D.3
Hardin, M.T.4
Anderson, G.5
Cohen, D.J.6
-
11
-
-
0030042516
-
Analgesic efficacy of the κ-receptor agonist, enadoline, in dental surgery pain
-
PANDE AC, PYKE RE, GREINER M, COOPER SA, BENJAMIN R, PIERCE MW: Analgesic efficacy of the κ-receptor agonist, enadoline, in dental surgery pain. Clin. Neuropharmacol. (1996a) 19:92-97.
-
(1996)
Clin. Neuropharmacol.
, vol.19
, pp. 92-97
-
-
Pande, A.C.1
Pyke, R.E.2
Greiner, M.3
Cooper, S.A.4
Benjamin, R.5
Pierce, M.W.6
-
12
-
-
0029790082
-
Analgesic efficacy of enadoline versus placebo or morphine in postsurgical pain
-
PANDE AC, PYKE RE, GREINER M, WIDEMAN GL, BENJAMIN R, PIERCE MW: Analgesic efficacy of enadoline versus placebo or morphine in postsurgical pain. Clin. Neuropharmacol. (1996b) 19:451-456.
-
(1996)
Clin. Neuropharmacol.
, vol.19
, pp. 451-456
-
-
Pande, A.C.1
Pyke, R.E.2
Greiner, M.3
Wideman, G.L.4
Benjamin, R.5
Pierce, M.W.6
-
13
-
-
0034873586
-
Enadoline, a selective κ-opioid agonist: Comparison with butorphanol and hydromorphone in humans
-
WALSH SL, STRAIN EC, ABREU ME, BIGELOW GE: Enadoline, a selective κ-opioid agonist: comparison with butorphanol and hydromorphone in humans. Psychopharmacol. (2001) 157:151-162.
-
(2001)
Psychopharmacol.
, vol.157
, pp. 151-162
-
-
Walsh, S.L.1
Strain, E.C.2
Abreu, M.E.3
Bigelow, G.E.4
-
14
-
-
2142698060
-
Prolonged opportunity for ischemic neuroprotection with selective κ-opioid receptor agonist in rats
-
CHEN T-Y, GOYAGI T, TOUNG TJK et al: Prolonged opportunity for ischemic neuroprotection with selective κ-opioid receptor agonist in rats. Stroke (2004) 35:1180-1185.
-
(2004)
Stroke
, vol.35
, pp. 1180-1185
-
-
Chen, T.-Y.1
Goyagi, T.2
Toung, T.J.K.3
-
15
-
-
1442323946
-
Opioids and renal function
-
MERCADANTE S, ARCURI E: Opioids and renal function. J. Pain (2004) 5:2-19.
-
(2004)
J. Pain
, vol.5
, pp. 2-19
-
-
Mercadante, S.1
Arcuri, E.2
-
16
-
-
0037380025
-
Activation of κ-opioid receptors inhibits pruritus evoked by subcutaneous or intrathecal administration of morphine in monkeys
-
KO MCH, LEE H, SONG MS et al.: Activation of κ-opioid receptors inhibits pruritus evoked by subcutaneous or intrathecal administration of morphine in monkeys. J. Pharmacol. Exp. Ther. (2003) 305:173-179.
-
(2003)
J. Pharmacol. Exp. Ther.
, vol.305
, pp. 173-179
-
-
Ko, M.C.H.1
Lee, H.2
Song, M.S.3
-
17
-
-
5044237216
-
Prospects for a novel κ-opioid receptor agonist, TRK-820, in uremic pruritus
-
KUMAGAI H, SARUTA T, MATSUKAWA S, UTSUMI J: Prospects for a novel κ-opioid receptor agonist, TRK-820, in uremic pruritus. Basic Clin. Dermatol. (2004) 27:279-286.
-
(2004)
Basic Clin. Dermatol.
, vol.27
, pp. 279-286
-
-
Kumagai, H.1
Saruta, T.2
Matsukawa, S.3
Utsumi, J.4
-
18
-
-
0042190068
-
Effect of acute and chronic administration of U50,488, a κ-opioid receptor agonist, in 6-OHDA-lesioned rats chronically treated with levodopa
-
MARIN C, BOVE J, BONASTRE M, TOLOSA E: Effect of acute and chronic administration of U50,488, a κ-opioid receptor agonist, in 6-OHDA-lesioned rats chronically treated with levodopa. Exp. Neurology (2003) 183:66-73.
-
(2003)
Exp. Neurology
, vol.183
, pp. 66-73
-
-
Marin, C.1
Bove, J.2
Bonastre, M.3
Tolosa, E.4
-
19
-
-
0035199592
-
Antiamnesic effect of the two novel κ-opioid agonists, VA-100 and VA-101, in the mouse passive avoidance test
-
GHELARDINI C, GALEOTTI N, DI CESARE MANNELLI L, CAPPELLI A, ANZINI M, BARTOLINI A: Antiamnesic effect of the two novel κ-opioid agonists, VA-100 and VA-101, in the mouse passive avoidance test. Drug Dev. Res. (2001) 54:12-18.
-
(2001)
Drug Dev. Res.
, vol.54
, pp. 12-18
-
-
Ghelardini, C.1
Galeotti, N.2
Di Cesare Mannelli, L.3
Cappelli, A.4
Anzini, M.5
Bartolini, A.6
-
21
-
-
0032437428
-
Effects of κ-opioid agonists on cocaine- and food-maintained responding by rhesus monkeys
-
MELLO NK, NEGUS SS: Effects of κ-opioid agonists on cocaine- and food-maintained responding by rhesus monkeys. J. Pharmacol. Exp. Ther. (1998) 286:812-824.
-
(1998)
J. Pharmacol. Exp. Ther.
, vol.286
, pp. 812-824
-
-
Mello, N.K.1
Negus, S.S.2
-
22
-
-
0029001901
-
κ-Opioid inhibition of morphine and cocaine self-administration in rats
-
GLICK SD, MAISSONEUVE IM, RAUCCI J, ARCHER S: κ-Opioid inhibition of morphine and cocaine self-administration in rats. Brain Res. (1995) 681:147-152.
-
(1995)
Brain Res.
, vol.681
, pp. 147-152
-
-
Glick, S.D.1
Maissoneuve, I.M.2
Raucci, J.3
Archer, S.4
-
23
-
-
0036082407
-
8-Carboxamidocyclazocine: A long-acting, novel benzomorphan
-
BIDLACK JM, COHEN DJ, MCLAUGHLIN JP, LOU R, YE Y, WENTLAND MP: 8-Carboxamidocyclazocine: a long-acting, novel benzomorphan. J. Pharmacol. Exp. Ther. (2002) 302:374-380
-
(2002)
J. Pharmacol. Exp. Ther.
, vol.302
, pp. 374-380
-
-
Bidlack, J.M.1
Cohen, D.J.2
Mclaughlin, J.P.3
Lou, R.4
Ye, Y.5
Wentland, M.P.6
-
24
-
-
0026639243
-
The role of μ- and κ-opioid receptors in cocaine-induced conditioned place preference
-
SUZUKI T, SHIOZAKI Y, MASUKAWA Y, MISAWA M, NAGASE H: The role of μ- and κ-opioid receptors in cocaine-induced conditioned place preference. Jpn. J. Pharmacol. (1992) 58:435-442.
-
(1992)
Jpn. J. Pharmacol.
, vol.58
, pp. 435-442
-
-
Suzuki, T.1
Shiozaki, Y.2
Masukawa, Y.3
Misawa, M.4
Nagase, H.5
-
25
-
-
0035840301
-
κ-Opioid receptor stimulation decreases amphetamine-induced behavior and neuropeptide mRNA expression in the striatum
-
TZAFERIS JA, MCGINTY JF: κ-Opioid receptor stimulation decreases amphetamine-induced behavior and neuropeptide mRNA expression in the striatum. Mol. Brain Res. (2001) 93:27-35.
-
(2001)
Mol. Brain Res.
, vol.93
, pp. 27-35
-
-
Tzaferis, J.A.1
Mcginty, J.F.2
-
26
-
-
0027990505
-
Opioid peptides selective for receptor types modulate cocaine-induced behavioural responses in mice
-
UKAI M, MIZUTANI M, KAMEYAMA T: Opioid peptides selective for receptor types modulate cocaine-induced behavioural responses in mice. Yakubutsu Seishin Kodo (1994) 14:153-159.
-
(1994)
Yakubutsu Seishin Kodo
, vol.14
, pp. 153-159
-
-
Ukai, M.1
Mizutani, M.2
Kameyama, T.3
-
27
-
-
0029155816
-
The effects of the κ-agonist U-50,488 on cocaine-induced conditioned and unconditioned behaviours and Fos immunoreactivity
-
CRAWFORD CA, MCDOUGALL SA, BOLANOS CA, HALL S, BERGER SP: The effects of the κ-agonist U-50,488 on cocaine-induced conditioned and unconditioned behaviours and Fos immunoreactivity. Psychopharmacology (1995) 120:392-399.
-
(1995)
Psychopharmacology
, vol.120
, pp. 392-399
-
-
Crawford, C.A.1
Mcdougall, S.A.2
Bolanos, C.A.3
Hall, S.4
Berger, S.P.5
-
28
-
-
0030087946
-
κ-Opioid receptor agonists prevent sensitization to the conditioned rewarding effects of cocaine
-
SHIPPENBERG TS, LEFEVOUR A, HEIDBREDER CH: κ-Opioid receptor agonists prevent sensitization to the conditioned rewarding effects of cocaine. J. Pharmacol. Exp. Ther. (1996) 276:545-554.
-
(1996)
J. Pharmacol. Exp. Ther.
, vol.276
, pp. 545-554
-
-
Shippenberg, T.S.1
Lefevour, A.2
Heidbreder, C.H.3
-
29
-
-
0036241902
-
Effects of newly synthesised κ-opioid receptor agonist, TRK-820, on the discriminative stimulus and rewarding effects of cocaine in rats
-
MORI T, NOMURA M, NAGASE H, SUZUKI T: Effects of newly synthesised κ-opioid receptor agonist, TRK-820, on the discriminative stimulus and rewarding effects of cocaine in rats. Psychopharmacology (2002) 161:17-22.
-
(2002)
Psychopharmacology
, vol.161
, pp. 17-22
-
-
Mori, T.1
Nomura, M.2
Nagase, H.3
Suzuki, T.4
-
30
-
-
0033929804
-
Interactions between κ-opioid agonists and cocaine - Preclinical studies. New medications for drug abuse
-
MELLO NK, NEGUS SS: Interactions between κ-opioid agonists and cocaine - preclinical studies. New medications for drug abuse. Ann. NY Acad. Sci. (2000) 909:104-132.
-
(2000)
Ann. NY Acad. Sci.
, vol.909
, pp. 104-132
-
-
Mello, N.K.1
Negus, S.S.2
-
31
-
-
0036263977
-
Effects of bremazocine on self-administration of smoked cocaine base and orally delivered ethanol, phencyclidine, saccharin, and food in rhesus monkeys: A behavioural economic analysis
-
COSGROVE KP, CARROLL ME: Effects of bremazocine on self-administration of smoked cocaine base and orally delivered ethanol, phencyclidine, saccharin, and food in rhesus monkeys: A behavioural economic analysis. J. Pharmacol. Exp. Ther. (2002) 301 993-1002.
-
(2002)
J. Pharmacol. Exp. Ther.
, vol.301
, pp. 993-1002
-
-
Cosgrove, K.P.1
Carroll, M.E.2
-
32
-
-
0001381990
-
Cyclazocine: Comparison to hydromorphone and interaction with cocaine
-
PRESTON KI, UMBRICHT A, SCHROEDER JR, ABREU M, PICKWORTH WB: Cyclazocine: comparison to hydromorphone and interaction with cocaine. Drug Med. Depend. (2001) 63(Suppl.1):S126.
-
(2001)
Drug Med. Depend.
, vol.63
, Issue.SUPPL. 1
-
-
Preston, K.I.1
Umbricht, A.2
Schroeder, J.R.3
Abreu, M.4
Pickworth, W.B.5
-
33
-
-
0029994263
-
Application of the message-address concept of the docking of naltrexone and selective naltrexone-derived opioid antagonists into opioid receptor models
-
METZGER TG, PATERLINI MG, PORTOGHESE PS, FERGUSON DM: Application of the message-address concept of the docking of naltrexone and selective naltrexone-derived opioid antagonists into opioid receptor models. Neurochem. Res. (1996) 21:1287-1294.
-
(1996)
Neurochem. Res.
, vol.21
, pp. 1287-1294
-
-
Metzger, T.G.1
Paterlini, M.G.2
Portoghese, P.S.3
Ferguson, D.M.4
-
34
-
-
7844249248
-
Conformational analysis and automated receptor docking of selective arylacetamide-based κ-opioid agonists
-
SUBRAMANIAN G, PATERLINI MG, LARSON DL, PORTOGHESE PS, FERGUSON DM: Conformational analysis and automated receptor docking of selective arylacetamide-based κ-opioid agonists. J. Med. Chem. (1998) 41:4777-4789.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 4777-4789
-
-
Subramanian, G.1
Paterlini, M.G.2
Larson, D.L.3
Portoghese, P.S.4
Ferguson, D.M.5
-
35
-
-
0037431393
-
Mechanism of action of the diazabicyclononanone-type κ-agonists
-
HOLZGRABE U, BRANDT W: Mechanism of action of the diazabicyclononanone-type κ-agonists. (2003) 46:1383-1389.
-
(2003)
, vol.46
, pp. 1383-1389
-
-
Holzgrabe, U.1
Brandt, W.2
-
36
-
-
18244375055
-
3-Aryl pyridone derivatives. Potent and selective κ-opioid receptor agonists
-
SEMPLE G, ANDERSON BM, CHHAJLANI V et al.: 3-Aryl pyridone derivatives. Potent and selective κ-opioid receptor agonists. Bioorg. Med. Chem. Lett (2002) 12:197-200.
-
(2002)
Bioorg. Med. Chem. Lett
, vol.12
, pp. 197-200
-
-
Semple, G.1
Anderson, B.M.2
Chhajlani, V.3
-
37
-
-
0037463770
-
Synthesis and biological activity of κ-opioid receptor agonists. Part 2: Preparation of 3-aryl-2-pyridone analogues generated by solution- and solid-phase parallel synthesis methods
-
SEMPLE G, ANDERSON BM, CHHAJLANI V et al.: Synthesis and biological activity of κ-opioid receptor agonists. Part 2: Preparation of 3-aryl-2-pyridone analogues generated by solution- and solid-phase parallel synthesis methods. Bioorg. Med. Chem. Lett. (2003) 13:1141-1145.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 1141-1145
-
-
Semple, G.1
Anderson, B.M.2
Chhajlani, V.3
-
38
-
-
0035927440
-
Transformation of a κ-opioid receptor antagonist to a κ-agonist by transfer of a guanidinium group from the 5′- to 6′-position of naltrindole
-
SHARMA SK, JONES RM, METZGER TG et al.: Transformation of a κ-opioid receptor antagonist to a κ-agonist by transfer of a guanidinium group from the 5′- to 6′-position of naltrindole. J. Med. Chem. (2001) 44: 2073-2079.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 2073-2079
-
-
Sharma, S.K.1
Jones, R.M.2
Metzger, T.G.3
-
40
-
-
0026674117
-
The formalin test: An evaluation of the method
-
TJØLSEN A, BERGE O-G, HUNSKAAR S, ROSLAND JH, HOLE K: The formalin test: an evaluation of the method. Pain (1992) 51 5-17.
-
(1992)
Pain
, vol.51
, pp. 5-17
-
-
Tjølsen, A.1
Berge, O.-G.2
Hunskaar, S.3
Rosland, J.H.4
Hole, K.5
-
41
-
-
0025805581
-
Standardization of the rat paw formalin test for the evaluation of analgesics
-
WHEELER-ACE TO H, COWAN A: Standardization of the rat paw formalin test for the evaluation of analgesics. Psychopharmacol. (1991) 104:35-44.
-
(1991)
Psychopharmacol.
, vol.104
, pp. 35-44
-
-
Wheeler-Ace, T.O.H.1
Cowan, A.2
-
42
-
-
0034694363
-
Arylacetamides as peripherally restricted κ-opioid receptor agonists
-
KUMAR V, MARELLA MA, CORTES-BURGOS L et al.: Arylacetamides as peripherally restricted κ-opioid receptor agonists. Bioorg. Med. Chem. Lett. (2000) 10:2567-2570.
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 2567-2570
-
-
Kumar, V.1
Marella, M.A.2
Cortes-Burgos, L.3
-
44
-
-
0028987769
-
Antinociceptive effect of a κ-opioid receptor agonist that minimally crosses the blood-brain barrier (ICI-204448) in a rat model of mononeuropathy
-
KEITA H, KAYSER V, GUILBAUD G: Antinociceptive effect of a κ-opioid receptor agonist that minimally crosses the blood-brain barrier (ICI-204448) in a rat model of mononeuropathy. Eur. J. Pharmacol. (1995) 277: 275-280.
-
(1995)
Eur. J. Pharmacol.
, vol.277
, pp. 275-280
-
-
Keita, H.1
Kayser, V.2
Guilbaud, G.3
-
45
-
-
0035848380
-
8-Carboxamidocyclazocine analogues: Redefining the structure-activity relationships of 2,6-methano-3-benzazocines
-
WENTLAND MP, LOU R, YE Y et al.: 8-Carboxamidocyclazocine analogues: Redefining the structure-activity relationships of 2,6-methano-3-benzazocines. Bioorg. Med. Chem. Lett. (2001) 11:623-626.
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 623-626
-
-
Wentland, M.P.1
Lou, R.2
Ye, Y.3
-
46
-
-
0037468407
-
Synthesis and opioid receptor binding affinities of 8-amino-2,6-methano-3-benzazocines
-
WENTLAND MP, YE Y, CIOFFI C et al.: Synthesis and opioid receptor binding affinities of 8-amino-2,6-methano-3-benzazocines. J. Med. Chem. (2003) 46:838-849.
-
(2003)
J. Med. Chem.
, vol.46
, pp. 838-849
-
-
Wentland, M.P.1
Ye, Y.2
Cioffi, C.3
-
47
-
-
0034699499
-
Selective protection and functionalization of morphine: Synthesis and opioid receptor binding properties of 3-amino-3-desoxymorphine derivatives
-
WENTLAND MP, DUAN W, COHEN DJ, BIDLACK JM: Selective protection and functionalization of morphine: Synthesis and opioid receptor binding properties of 3-amino-3-desoxymorphine derivatives. J. Med. Chem. (2000) 43:3558-3565.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 3558-3565
-
-
Wentland, M.P.1
Duan, W.2
Cohen, D.J.3
Bidlack, J.M.4
-
48
-
-
0035833120
-
3-Carboxamido analogues of morphine and naltrexone: Synthesis and opioid receptor binding properties
-
WENTLAND MP, LOU R, DEHNHARDT CM et al.: 3-Carboxamido analogues of morphine and naltrexone: Synthesis and opioid receptor binding properties. Bioorg. Med. Chem. Lett. (2001) 11 1717-1721.
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 1717-1721
-
-
Wentland, M.P.1
Lou, R.2
Dehnhardt, C.M.3
-
50
-
-
0035935189
-
Mixed κ-agonists and μ agonists/antagonists as potential pharmacotherapeutics for cocaine abuse: Synthesis and opioid receptor binding affinity of N-substituted derivatives of morphinan
-
NEUMEYER JL, GU X-H, VAN VLIET LA et al.: Mixed κ-agonists and μ agonists/antagonists as potential pharmacotherapeutics for cocaine abuse: Synthesis and opioid receptor binding affinity of N-substituted derivatives of morphinan. Bioorg. Med. Chem. Lett. (2001) 11: 2735-2740.
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 2735-2740
-
-
Neumeyer, J.L.1
Gu, X.-H.2
Van Vliet, L.A.3
-
51
-
-
0347991961
-
10-Ketomorphinan and 3-substituted-3-desoxymorphinan analogues as mixed κ and μ-opioid ligands: Synthesis and biological evaluation of their binding affinity at opioid receptors
-
ZHANG A, XIONG W, BIDLACK JM et al.: 10-Ketomorphinan and 3-substituted-3-desoxymorphinan analogues as mixed κ and μ -opioid ligands: Synthesis and biological evaluation of their binding affinity at opioid receptors. J. Med. Chem. (2004) 47:165-174.
-
(2004)
J. Med. Chem.
, vol.47
, pp. 165-174
-
-
Zhang, A.1
Xiong, W.2
Bidlack, J.M.3
-
52
-
-
0023139286
-
Binaltorphimine and nor-binaltorphimine, potent and selective κ-opioid receptor antagonists
-
PORTOGHESE PS, LIPKOWSKI AW, TAKEMORI AE: Binaltorphimine and nor-binaltorphimine, potent and selective κ-opioid receptor antagonists. Life Sci. (1987) 40:1287-1292.
-
(1987)
Life Sci.
, vol.40
, pp. 1287-1292
-
-
Portoghese, P.S.1
Lipkowski, A.W.2
Takemori, A.E.3
-
53
-
-
0343191562
-
Potent and selective indolomorphinan antagonists of the κ-opioid receptor
-
STEVENS WC JR, JONES RM, SUBRAMANIAN G et al.: Potent and selective indolomorphinan antagonists of the κ-opioid receptor. J. Med. Chem. (2000) 43:2759-2769.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 2759-2769
-
-
Stevens Jr., W.C.1
Jones, R.M.2
Subramanian, G.3
-
54
-
-
0017620408
-
A short introductory review
-
SCHWYZER R: A short introductory review. Ann. NY Acad. Sci. (1997) 247:3-26.
-
(1997)
Ann. NY Acad. Sci.
, vol.247
, pp. 3-26
-
-
Schwyzer, R.1
-
55
-
-
0035811447
-
From models to molecules: Opioid receptor dimers, bivalent ligands and selective opioid receptor probes
-
PORTOGHESE PS: From models to molecules: Opioid receptor dimers, bivalent ligands and selective opioid receptor probes. J. Med. Chem. (2001) 44: 2259-2269.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 2259-2269
-
-
Portoghese, P.S.1
-
56
-
-
0035899186
-
Identification of the first trans-(3R,4R)-dimethyl-4-(3-hydroxyphenyl)piperidine derivative to possess highly potent and selective opioid κ-receptor antagonist activity
-
THOMAS JB, ATKINSON RN, ROTHMAN RB et al.: Identification of the first trans-(3R,4R -dimethyl-4-(3-hydroxyphenyl)piperidine derivative to possess highly potent and selective opioid κ-receptor antagonist activity. J. Med. Chem. (2001) 44:2687-2690.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 2687-2690
-
-
Thomas, J.B.1
Atkinson, R.N.2
Rothman, R.B.3
-
57
-
-
0037783998
-
Identification of (3R)-7-hydroxy-N-((1S)-1-{[3R,4R)-4-(3-hydroxyphenyl)-3,4-dimethyl-1- piperidinyl]methyl}-2-methylpropyl)-1,2,3,4-tetrahydro-3- isoquinolinecarboxamide as a novel potent and selective opioid κ-receptor antagonist
-
THOMAS JB, ATKINSON RN, VINSON NA et al.: Identification of (3R)-7-hydroxy-N-((1S -1-{[3R,4R -4-(3-hydroxyphenyl)-3,4-dimethyl-1- piperidinyl]methyl}-2-methylpropyl)-1,2,3,4-tetrahydro-3- isoquinolinecarboxamide as a novel potent and selective opioid κ-receptor antagonist. J. Med. Chem. (2003) 46:3127-3137.
-
(2003)
J. Med. Chem.
, vol.46
, pp. 3127-3137
-
-
Thomas, J.B.1
Atkinson, R.N.2
Vinson, N.A.3
-
58
-
-
0018135396
-
New structural concepts for structural antagonists defined in a 4-phenylpiperidine series
-
ZIMMERMAN DM, NICKANDER R, HORNG JS, WONG DT: New structural concepts for structural antagonists defined in a 4-phenylpiperidine series. Nature (1978) 275: 332-334.
-
(1978)
Nature
, vol.275
, pp. 332-334
-
-
Zimmerman, D.M.1
Nickander, R.2
Horng, J.S.3
Wong, D.T.4
-
59
-
-
0036682415
-
Discovery of an opioid κ-receptor selective pure antagonist from a library of N-substituted 4β-methyl-5-(3-hydroxyphenyl )morphans
-
THOMAS JB, ATKINSON RN, NAMDEV N et al.: Discovery of an opioid κ-receptor selective pure antagonist from a library of N-substituted 4β-methyl-5-(3-hydroxyphenyl)morphans. J. Med. Chem. (2002) 45: 3524-3530.
-
(2002)
J. Med. Chem.
, vol.45
, pp. 3524-3530
-
-
Thomas, J.B.1
Atkinson, R.N.2
Namdev, N.3
-
60
-
-
0033530826
-
Synthesis and opiate receptor binding properties of 17-methyl-6,7-dehydro-3,14-dihydroxy-4,5α-epoxy-6,7:4′ ,5′- pyrimidinomorphinans
-
XU W, HUANG L-F, BAUER L, BHARGAVA HN, DUNN WJ III: Synthesis and opiate receptor binding properties of 17-methyl-6,7-dehydro-3,14-dihydroxy-4,5α-epoxy-6,7:4′ ,5′- pyrimidinomorphinans. Bioorg. Med. Chem. Lett. (1991) 9:3375-3380.
-
(1991)
Bioorg. Med. Chem. Lett.
, vol.9
, pp. 3375-3380
-
-
Xu, W.1
Huang, L.-F.2
Bauer, L.3
Bhargava, H.N.4
Dunn III, W.J.5
-
61
-
-
0037380025
-
Activation of κ-opioid receptors inhibits pruritus evoked by subcutaneous or intrathecal administration of morphine in monkeys
-
KO MCH, LEE H, SONG MS et al.: Activation of κ-opioid receptors inhibits pruritus evoked by subcutaneous or intrathecal administration of morphine in monkeys. J. Pharmacol. Exp. Ther. (2003) 305: 173-179.
-
(2003)
J. Pharmacol. Exp. Ther.
, vol.305
, pp. 173-179
-
-
Ko, M.C.H.1
Lee, H.2
Song, M.S.3
-
62
-
-
3042593116
-
The role of central μ opioid receptors in opioid-induced itch in primates
-
KO MCH, SONG MS, EDWARDS T et al.: The role of central μ opioid receptors in opioid-induced itch in primates. J. Pharmacol. Exp. Ther. (2004) 310:169-176.
-
(2004)
J. Pharmacol. Exp. Ther.
, vol.310
, pp. 169-176
-
-
Ko, M.C.H.1
Song, M.S.2
Edwards, T.3
-
63
-
-
0037169176
-
Antipruritic activity of the κ-opioid receptor agonist, TRK-820
-
TOGASHI Y, UMEUCHI H, OKANO K et al.: Antipruritic activity of the κ-opioid receptor agonist, TRK-820. Eur. J. Pharmacol. (2002) 435:259-264.
-
(2002)
Eur. J. Pharmacol.
, vol.435
, pp. 259-264
-
-
Togashi, Y.1
Umeuchi, H.2
Okano, K.3
-
64
-
-
0029564345
-
Irritable bladder syndrome in an animal model: A continuous monitoring study
-
GHONIEM GM, SHAABAN AM, CLARKE MR: Irritable bladder syndrome in an animal model: a continuous monitoring study. Neurourol. Urodyn. (1995) 14:657-665.
-
(1995)
Neurourol. Urodyn.
, vol.14
, pp. 657-665
-
-
Ghoniem, G.M.1
Shaaban, A.M.2
Clarke, M.R.3
-
65
-
-
0037381053
-
Antidepressant-like effects of κ-opioid receptor antagonists in the forced swim test in rats
-
MAGUE SD, PLIAKAS AM, TODTENKOPF MS et al.: Antidepressant-like effects of κ-opioid receptor antagonists in the forced swim test in rats. J. Pharmacol. Exp. Ther. (2003) 305 323-330.
-
(2003)
J. Pharmacol. Exp. Ther.
, vol.305
, pp. 323-330
-
-
Mague, S.D.1
Pliakas, A.M.2
Todtenkopf, M.S.3
-
66
-
-
0030751362
-
Novel developments with selective, non-peptidic κ-opioid receptor agonists
-
BARBER A, GOTTSCHLICH R: Novel developments with selective, non-peptidic κ-opioid receptor agonists. Exp. Opin. Investig. Drugs (1997) 6:1351-1368.
-
(1997)
Exp. Opin. Investig. Drugs
, vol.6
, pp. 1351-1368
-
-
Barber, A.1
Gottschlich, R.2
-
67
-
-
0344731442
-
Peripheral effects of the κ-opioid agonist EMD-61753 on pain and inflammation in rats and humans
-
MACHELSKA H, PFLUGER M, WEBER W et al. Peripheral effects of the κ-opioid agonist EMD-61753 on pain and inflammation in rats and humans. J. Pharmacol. Exp. Ther. (1999) 290:354-361.
-
(1999)
J. Pharmacol. Exp. Ther.
, vol.290
, pp. 354-361
-
-
Machelska, H.1
Pfluger, M.2
Weber, W.3
-
69
-
-
2442472275
-
Peripheral κ-opioid agonists for visceral pain
-
RIVIERE PJ: Peripheral κ-opioid agonists for visceral pain. Br. J. Pharmacol. (2004) 141:1331-1334.
-
(2004)
Br. J. Pharmacol.
, vol.141
, pp. 1331-1334
-
-
Riviere, P.J.1
-
70
-
-
0037223119
-
Analgesia from a peripherally active κ-opioid receptor agonist in patients with chronic pancreatitis
-
EISENACH JC, CARPENTER R, CURRY R: Analgesia from a peripherally active κ-opioid receptor agonist in patients with chronic pancreatitis. Pain (2003) 101:89-95.
-
(2003)
Pain
, vol.101
, pp. 89-95
-
-
Eisenach, J.C.1
Carpenter, R.2
Curry, R.3
-
71
-
-
0013931421
-
An experimental study in the treatment of narcotic addicts with cyclazocine
-
MARTIN WR, GORODETZKY CW, McLANE TK: An experimental study in the treatment of narcotic addicts with cyclazocine. Clin. Pharmacol. Ther. (1966) 455-464.
-
(1966)
Clin. Pharmacol. Ther.
, pp. 455-464
-
-
Martin, W.R.1
Gorodetzky, C.W.2
Mclane, T.K.3
|