메뉴 건너뛰기




Volumn 14, Issue 12, 2004, Pages 1725-1741

Kappa-opioid receptor ligands

Author keywords

opioid; Agonist; Antagonist; Mixed agonists; Therapeutic

Indexed keywords

3 [1 (3,4 DICHLORO N METHYLPHENYLACETAMIDO) 2 (1 PYRROLIDINYL)ETHYL]PHENOXYACETIC ACID; 3,4 DICHLORO N METHYL N [1 PHENYL 2 (1 PYRROLIDINYL)ETHYL]BENZENEACETAMIDE; 4,5 EPOXYINDOLOMORPHINAN DERIVATIVE; ACETAMIDE DERIVATIVE; ANALGESIC AGENT; ANTIHISTAMINIC AGENT; ANTINOCICEPTIVE AGENT; ASIMADOLINE; BENZOTHIAZOLINE DERIVATIVE; CYCLAZOCINE; CYCLORPHAN; KAPPA OPIATE RECEPTOR; KAPPA OPIATE RECEPTOR AGONIST; KAPPA OPIATE RECEPTOR ANTAGONIST; KETAZOCINE; LEVALLORPHAN; LEVORPHANOL; LIGAND; MORPHINAN DERIVATIVE; MORPHINE; MR 2003; N (TETRAHYDROFURFURYL)NORMETAZOCINE; NALFURAFINE; NALTREXONE; NALTRINDOLE; NORBINALTORPHIMINE; OXYMORPHONE; PIPERIDINE DERIVATIVE; PYRIDONE DERIVATIVE; SULFONAMIDE; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 10344221014     PISSN: 13543776     EISSN: None     Source Type: Journal    
DOI: 10.1517/13543776.14.12.1725     Document Type: Review
Times cited : (9)

References (72)
  • 2
    • 3242728388 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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
  • 5
    • 0017735536 scopus 로고
    • Endogenous opioid peptides: Multiple agonists and receptors
    • LORD JA, WATERFIELD AA, HUGHES J, KOSTERLITZ HW: Endogenous opioid peptides: multiple agonists and receptors. Nature (1977) 267:495-499.
    • (1977) Nature , vol.267 , pp. 495-499
    • Lord, J.A.1    Waterfield, A.A.2    Hughes, J.3    Kosterlitz, H.W.4
  • 6
    • 0013832249 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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
  • 13
    • 0034873586 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 21
    • 0032437428 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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
  • 24
    • 0026639243 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 33
    • 0029994263 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 41
    • 0025805581 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 43
    • 0024506654 scopus 로고
    • ICI 204448: A κ-opioid agonist with limited access to the CNS
    • SHAW JS, CARROLL JA, ALCOC P, MAIN BG: ICI 204448: a κ-opioid agonist with limited access to the CNS. Br J. Pharmacol. (1989) 96:986-992.
    • (1989) Br. J. Pharmacol. , vol.96 , pp. 986-992
    • Shaw, J.S.1    Carroll, J.A.2    Alcoc, P.3    Main, B.G.4
  • 44
    • 0028987769 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.