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Volumn 31, Issue 4, 2011, Pages 605-648

Development of nociceptin receptor (NOP) agonists and antagonists

Author keywords

Nociceptin; NOP receptor ligands; Opioids; Structure activity relationship

Indexed keywords

7 [4 (2,6 DICHLOROPHENYL) 1 PIPERIDINYLMETHYL] 6,7,8,9 TETRAHYDRO 1 METHYL 5H BENZOCYCLOHEPTEN 5 OL; 8 (2,3,3A,4,5,6 HEXAHYDRO 1H PHENALEN 1 YL) 1 PHENYL 1,3,8 TRIAZASPIRO[4.5]DECAN 4 ONE; [8 (1 NAPHTHYLMETHYL) 4 OXO 1 PHENYL 1,3,8 TRIAZASPIRO[4.5]DEC 3 YL]ACETIC ACID METHYL ESTER; BENZIMIDAZOLE DERIVATIVE; BUPRENORPHINE; CYCLOHEXYLAMINE DERIVATIVE; ETORPHINE; GLYCINE; GUANOSINE; INDOLE DERIVATIVE; LIGAND; N (4 AMINO 2 METHYL 6 QUINOLINYL) 2 (4 ETHYLPHENOXYMETHYL)BENZAMIDE; NALFURAFINE; NALOXONE BENZOYLHYDRAZONE; NHC 63 0532; NOCICEPTIN RECEPTOR AGONIST; NOCICEPTIN RECEPTOR ANTAGONIST; NORTROPANE DERIVATIVE; OPIATE AGONIST; PEPTIDE; PIMOZIDE; PIPERIDINE DERIVATIVE; POTASSIUM CHANNEL HERG; PYRROLE DERIVATIVE; QUINAZOLINE DERIVATIVE; RO 65 6570; SCH 221510; SPIROXATRINE; UNCLASSIFIED DRUG; UNINDEXED DRUG; W 212393; ZP 120;

EID: 79955786304     PISSN: 01986325     EISSN: 10981128     Source Type: Journal    
DOI: 10.1002/med.20197     Document Type: Article
Times cited : (45)

References (203)
  • 5
    • 0036632334 scopus 로고    scopus 로고
    • 1 receptor: Molecular pharmacology and signalling mechanisms
    • 1 receptor: Molecular pharmacology and signalling mechanisms. Neurosignals 2002;11:197-212.
    • (2002) Neurosignals , vol.11 , pp. 197-212
    • New, D.C.1    Wong, Y.H.2
  • 6
    • 0033817778 scopus 로고    scopus 로고
    • Cellular action of nociceptin: Transduction mechanisms
    • Hawes BE, Graziano MP, Lambert DG. Cellular action of nociceptin: Transduction mechanisms. Peptides 2000;21:961-967.
    • (2000) Peptides , vol.21 , pp. 961-967
    • Hawes, B.E.1    Graziano, M.P.2    Lambert, D.G.3
  • 9
    • 0033821476 scopus 로고    scopus 로고
    • Tissue distribution of the opioid receptor-like (ORL1) receptor
    • Mollereau C, Mouledous L. Tissue distribution of the opioid receptor-like (ORL1) receptor. Peptides 2000;21:907-917.
    • (2000) Peptides , vol.21 , pp. 907-917
    • Mollereau, C.1    Mouledous, L.2
  • 10
    • 3042682601 scopus 로고    scopus 로고
    • Intradermal nociceptin elicits itch-associated responses through leukotriene B(4) in mice
    • Andoh T, Yageta Y, Takeshima H, Kuraishi Y. Intradermal nociceptin elicits itch-associated responses through leukotriene B(4) in mice. J Invest Dermatol 2004;123:196-201.
    • (2004) J Invest Dermatol , vol.123 , pp. 196-201
    • Andoh, T.1    Yageta, Y.2    Takeshima, H.3    Kuraishi, Y.4
  • 12
    • 0034850298 scopus 로고    scopus 로고
    • The molecular and behavioral pharmacology of the orphanin FQ/nociceptin peptide and receptor family
    • Mogil JS, Pasternak GW. The molecular and behavioral pharmacology of the orphanin FQ/nociceptin peptide and receptor family. Pharmacol Rev 2001;53:381-415.
    • (2001) Pharmacol Rev , vol.53 , pp. 381-415
    • Mogil, J.S.1    Pasternak, G.W.2
  • 14
    • 48749095410 scopus 로고    scopus 로고
    • The nociceptin/orphanin FQ receptor: A target with a broad therapeutical potential
    • Lambert DG. The nociceptin/orphanin FQ receptor: A target with a broad therapeutical potential. Nat Rev Drug Discov 2008;7:694-710.
    • (2008) Nat Rev Drug Discov , vol.7 , pp. 694-710
    • Lambert, D.G.1
  • 15
    • 18144431042 scopus 로고    scopus 로고
    • Recent advances towards the discovery of ORL-1 receptor agonists and antagonists
    • Bignan GC, Connoly PJ, Middleton SA. Recent advances towards the discovery of ORL-1 receptor agonists and antagonists. Expert Opin Ther Pat 2005;15:357-388.
    • (2005) Expert Opin Ther Pat , vol.15 , pp. 357-388
    • Bignan, G.C.1    Connoly, P.J.2    Middleton, S.A.3
  • 16
    • 33750326776 scopus 로고    scopus 로고
    • Daily intravesical instillation of 1mg nociceptin/orphanin FQ for the control of neurogenic detrusor overactivity: A multicenter, placebo controlled, randomized exploratory study
    • Lazzeri M, Calò G, Spinelli M, Malaguti S, Guerrini R, Salvadori S, Beneforti P, Regoli D, Turini D. Daily intravesical instillation of 1mg nociceptin/orphanin FQ for the control of neurogenic detrusor overactivity: A multicenter, placebo controlled, randomized exploratory study. J Urol 2006;176:2098-2102.
    • (2006) J Urol , vol.176 , pp. 2098-2102
    • Lazzeri, M.1    Calò, G.2    Spinelli, M.3    Malaguti, S.4    Guerrini, R.5    Salvadori, S.6    Beneforti, P.7    Regoli, D.8    Turini, D.9
  • 17
    • 4644245300 scopus 로고    scopus 로고
    • Buprenorphine: A unique drug with complex pharmacology
    • Lufty K, Cowan A. Buprenorphine: A unique drug with complex pharmacology. Curr Neuropharmacol 2004;2:395-402.
    • (2004) Curr Neuropharmacol , vol.2 , pp. 395-402
    • Lufty, K.1    Cowan, A.2
  • 19
    • 79959573799 scopus 로고    scopus 로고
  • 22
    • 0035524063 scopus 로고    scopus 로고
    • Non peptidic ligands at the opioid receptor like-1 (ORL-1)
    • Barlocco D, Toma L, Cignarella G. Non peptidic ligands at the opioid receptor like-1 (ORL-1). Mini Rev Med Chem 2001;1:363-375.
    • (2001) Mini Rev Med Chem , vol.1 , pp. 363-375
    • Barlocco, D.1    Toma, L.2    Cignarella, G.3
  • 23
    • 0035057560 scopus 로고    scopus 로고
    • Lead generation and lead optimisation approaches in the discovery of selective, non-peptide ORL-1 receptor agonists and antagonists
    • Ronzoni S, Peretto I, Giardina GAM. Lead generation and lead optimisation approaches in the discovery of selective, non-peptide ORL-1 receptor agonists and antagonists. Expert Opin Ther Pat 2001;11:525-546.
    • (2001) Expert Opin Ther Pat , vol.11 , pp. 525-546
    • Ronzoni, S.1    Peretto, I.2    Giardina, G.A.M.3
  • 24
    • 0037498440 scopus 로고    scopus 로고
    • Peptide and non peptide ligands for the nociceptin/orphanin FQ receptor ORL1: Research tools and potential therapeutic agents
    • Zaveri N. Peptide and non peptide ligands for the nociceptin/orphanin FQ receptor ORL1: Research tools and potential therapeutic agents. Life Sci 2003;73:663-678.
    • (2003) Life Sci , vol.73 , pp. 663-678
    • Zaveri, N.1
  • 25
    • 0343150924 scopus 로고    scopus 로고
    • Orphanin FQ: Receptor binding and analog structure activity relationships in rat brain
    • Dooley CT, Houghten RA. Orphanin FQ: Receptor binding and analog structure activity relationships in rat brain. Life Sci 1996;59:PL23-PL29.
    • (1996) Life Sci , vol.59
    • Dooley, C.T.1    Houghten, R.A.2
  • 26
    • 0342726574 scopus 로고    scopus 로고
    • Structure-activity relationship studies on the novel neuropeptide orphanin FQ
    • Reinscheid RK, Ardati A, Monsma FJ, Jr, Civelli O. Structure-activity relationship studies on the novel neuropeptide orphanin FQ. J Biol Chem 1996;271:14163-14168.
    • (1996) J Biol Chem , vol.271 , pp. 14163-14168
    • Reinscheid, R.K.1    Ardati, A.2    Monsma Jr, F.J.3    Civelli, O.4
  • 27
    • 0031577964 scopus 로고    scopus 로고
    • Recognition and activation of the opioid receptor-like ORL1 receptor by nociceptin, nociceptin analogs and opioids
    • Butour JL, Moisand C, Mazarguil H, Mollereau C, Meunier JC. Recognition and activation of the opioid receptor-like ORL1 receptor by nociceptin, nociceptin analogs and opioids. Eur J Pharmacol 1997;321:97-103.
    • (1997) Eur J Pharmacol , vol.321 , pp. 97-103
    • Butour, J.L.1    Moisand, C.2    Mazarguil, H.3    Mollereau, C.4    Meunier, J.C.5
  • 28
    • 0033429262 scopus 로고    scopus 로고
    • Structure-activity studies on nociceptin/orphanin FQ: From full agonist, to partial agonist, to pure antagonist
    • Salvadori S, Guerrini R, Calò G, Regoli D. Structure-activity studies on nociceptin/orphanin FQ: From full agonist, to partial agonist, to pure antagonist. Farmaco 1999;54:810-825.
    • (1999) Farmaco , vol.54 , pp. 810-825
    • Salvadori, S.1    Guerrini, R.2    Calò, G.3    Regoli, D.4
  • 29
    • 0029796366 scopus 로고    scopus 로고
    • Sensitivity of opioid receptor-like receptor ORL-1 for chemical modification on nociceptin, a naturally occurring nociceptive peptide
    • Shimohigashi Y, Hatano R, Fujita T, Nakashima R, Nose T, Sujaku T, Saigo A, Shinjo K, Nagahisa A. Sensitivity of opioid receptor-like receptor ORL-1 for chemical modification on nociceptin, a naturally occurring nociceptive peptide. J Biol Chem 1996;271:23642-23645.
    • (1996) J Biol Chem , vol.271 , pp. 23642-23645
    • Shimohigashi, Y.1    Hatano, R.2    Fujita, T.3    Nakashima, R.4    Nose, T.5    Sujaku, T.6    Saigo, A.7    Shinjo, K.8    Nagahisa, A.9
  • 31
    • 0031006367 scopus 로고    scopus 로고
    • Address and message sequences for the nociceptin receptor: A structure-activity study of nociceptin-(1-13)-peptide amide
    • Guerrini R, Calò G, Rizzi A, Bianchi C, Lazarus LH, Salvadori S, Temussi PA, Regoli D. Address and message sequences for the nociceptin receptor: A structure-activity study of nociceptin-(1-13)-peptide amide. J Med Chem 1997;40:1789-1793.
    • (1997) J Med Chem , vol.40 , pp. 1789-1793
    • Guerrini, R.1    Calò, G.2    Rizzi, A.3    Bianchi, C.4    Lazarus, L.H.5    Salvadori, S.6    Temussi, P.A.7    Regoli, D.8
  • 41
    • 53449086268 scopus 로고    scopus 로고
    • Synergistic effect of basic residues at positions 14-15 of nociceptin on binding affinity and receptor activation
    • Okada K, Isozaki K, Li J, Matsushima A, Nose T, Costa T, Shimohigashi Y. Synergistic effect of basic residues at positions 14-15 of nociceptin on binding affinity and receptor activation. Bioorg Med Chem 2008;16:9261-9267.
    • (2008) Bioorg Med Chem , vol.16 , pp. 9261-9267
    • Okada, K.1    Isozaki, K.2    Li, J.3    Matsushima, A.4    Nose, T.5    Costa, T.6    Shimohigashi, Y.7
  • 44
    • 20444428365 scopus 로고    scopus 로고
    • Synthesis and biological studies of nociceptin derivatives containing the DTPA chelating group for further labeling with therapeutic radionuclides
    • Ligeti M, Gündüz Ö, Magyar A, Kató E, Rónai AZ, Vita C, Varga I, Hudecz F, Tóth G, Borsodi A, Benyhe S. Synthesis and biological studies of nociceptin derivatives containing the DTPA chelating group for further labeling with therapeutic radionuclides. Peptides 2005;26:1159-1166.
    • (2005) Peptides , vol.26 , pp. 1159-1166
    • Ligeti, M.1    Gündüz, O.2    Magyar, A.3    Kató, E.4    Rónai, A.Z.5    Vita, C.6    Varga, I.7    Hudecz, F.8    Tóth, G.9    Borsodi, A.10    Benyhe, S.11
  • 48
    • 79959559216 scopus 로고    scopus 로고
    • Conformationally constrained peptides that bind the ORL-1 receptor. Patent EP 1927858 A1, Euro-Celtique S.A.
    • Kyle DJ. Conformationally constrained peptides that bind the ORL-1 receptor. Patent EP 1927858 A1, Euro-Celtique S.A., 2005.
    • (2005)
    • Kyle, D.J.1
  • 49
    • 0037153197 scopus 로고    scopus 로고
    • Novel, potent ORL-1 receptor agonist peptides containing α-helix-promoting conformational constraints
    • Zhang C, Miller W, Valenzano KJ, Kyle DJ. Novel, potent ORL-1 receptor agonist peptides containing α-helix-promoting conformational constraints. J Med Chem 2002;45:5280-5286.
    • (2002) J Med Chem , vol.45 , pp. 5280-5286
    • Zhang, C.1    Miller, W.2    Valenzano, K.J.3    Kyle, D.J.4
  • 51
    • 23644438900 scopus 로고    scopus 로고
    • Structure-activity studies on different modifications of nociceptin/orphanin FQ: Identification of highly potent agonists and antagonists of its receptor
    • Chang M, Peng YL, Dong SL, Han RW, Li W, Yang DJ, Chen Q, Wang R. Structure-activity studies on different modifications of nociceptin/orphanin FQ: Identification of highly potent agonists and antagonists of its receptor. Regul Pept 2005;130:116-122.
    • (2005) Regul Pept , vol.130 , pp. 116-122
    • Chang, M.1    Peng, Y.L.2    Dong, S.L.3    Han, R.W.4    Li, W.5    Yang, D.J.6    Chen, Q.7    Wang, R.8
  • 53
    • 15944405701 scopus 로고    scopus 로고
    • The interaction of highly helical structural mutants with the NOP receptor discloses the role of the address domain of nociceptin/orphanin FQ
    • Tancredi T, Carrà G, Guerrini R, Arduin M, Calò G, Regoli D, Salvadori S, Temussi PA. The interaction of highly helical structural mutants with the NOP receptor discloses the role of the address domain of nociceptin/orphanin FQ. Chem Eur J 2005;11:2061-2070.
    • (2005) Chem Eur J , vol.11 , pp. 2061-2070
    • Tancredi, T.1    Carrà, G.2    Guerrini, R.3    Arduin, M.4    Calò, G.5    Regoli, D.6    Salvadori, S.7    Temussi, P.A.8
  • 55
    • 0035829411 scopus 로고    scopus 로고
    • Structure-activity studies on nociceptin analogues: ORL1 receptor binding and biological activity of cyclic disulfide-containing analogues of nociceptin peptides
    • Ambo A, Hamazaki N, Yamada Y, Nakata E, Sasaki Y. Structure-activity studies on nociceptin analogues: ORL1 receptor binding and biological activity of cyclic disulfide-containing analogues of nociceptin peptides. J Med Chem 2001;44:4015-4018.
    • (2001) J Med Chem , vol.44 , pp. 4015-4018
    • Ambo, A.1    Hamazaki, N.2    Yamada, Y.3    Nakata, E.4    Sasaki, Y.5
  • 57
    • 49449099743 scopus 로고    scopus 로고
    • High affinity conformationally constrained nociceptin/orphaninFQ(1-13)amide analogues
    • Charoenchai L, Wang H, Wang JB, Aldrich JV. High affinity conformationally constrained nociceptin/orphaninFQ(1-13)amide analogues. J Med Chem 2008;51:4385-4387.
    • (2008) J Med Chem , vol.51 , pp. 4385-4387
    • Charoenchai, L.1    Wang, H.2    Wang, J.B.3    Aldrich, J.V.4
  • 60
    • 0034634223 scopus 로고    scopus 로고
    • Retro-nociceptin methylester, a peptide with analgesic and memory-enhancing activity
    • Jinsmaa Y, Takahashi M, Fukunaga H, Yoshikawa M. Retro-nociceptin methylester, a peptide with analgesic and memory-enhancing activity. Life Sci 2000;67:3095-3101.
    • (2000) Life Sci , vol.67 , pp. 3095-3101
    • Jinsmaa, Y.1    Takahashi, M.2    Fukunaga, H.3    Yoshikawa, M.4
  • 63
    • 0033821760 scopus 로고    scopus 로고
    • The nociceptin/orphaninFQ receptor ligand acetyl-RYYRIK-amide exhibit antagonistic and agonistic properties
    • Berger H, Bigoni R, Albrecht E, Richter RM, Krause E, Bienert M, Calò G. The nociceptin/orphaninFQ receptor ligand acetyl-RYYRIK-amide exhibit antagonistic and agonistic properties. Peptides 2000;21:1131-1139.
    • (2000) Peptides , vol.21 , pp. 1131-1139
    • Berger, H.1    Bigoni, R.2    Albrecht, E.3    Richter, R.M.4    Krause, E.5    Bienert, M.6    Calò, G.7
  • 64
    • 79959542680 scopus 로고    scopus 로고
    • Peptide conjugates modified N- and/or C-terminally by short charged peptide chains. Patent WO 01/98324 A1. Zealand Pharmaceuticals A/S.
    • Larsen BD, Petersen JS, Kapusta DR, Harlow KW. Peptide conjugates modified N- and/or C-terminally by short charged peptide chains. Patent WO 01/98324 A1. Zealand Pharmaceuticals A/S. 2001.
    • (2001)
    • Larsen, B.D.1    Petersen, J.S.2    Kapusta, D.R.3    Harlow, K.W.4
  • 65
    • 0036792738 scopus 로고    scopus 로고
    • Pharmacological characterization of the novel nociceptin/orphaninFQ receptor ligand, ZP120: In vitro and in vivo studies in mice
    • Rizzi A, Rizzi D, Marzola G, Regoli D, Larsen BD, Petersen JS, Calò G. Pharmacological characterization of the novel nociceptin/orphaninFQ receptor ligand, ZP120: In vitro and in vivo studies in mice. Br J Pharmacol 2002;137:369-374.
    • (2002) Br J Pharmacol , vol.137 , pp. 369-374
    • Rizzi, A.1    Rizzi, D.2    Marzola, G.3    Regoli, D.4    Larsen, B.D.5    Petersen, J.S.6    Calò, G.7
  • 66
    • 22944455872 scopus 로고    scopus 로고
    • Pharmacodynamic characterization of ZP120 (Ac-RYYRWKKKKKKK-NH2), a novel, functionally selective nociceptin/orphaninFQ receptor partial agonist with sodium-potassium sparing aquaretic activity
    • Kapusta DR, Thorkildsen G, Kenigs VA, Meier E, Vinge MM, Quist C, Petersen JS. Pharmacodynamic characterization of ZP120 (Ac-RYYRWKKKKKKK-NH2), a novel, functionally selective nociceptin/orphaninFQ receptor partial agonist with sodium-potassium sparing aquaretic activity. J Pharmacol Exp Ther 2005;314:652-660.
    • (2005) J Pharmacol Exp Ther , vol.314 , pp. 652-660
    • Kapusta, D.R.1    Thorkildsen, G.2    Kenigs, V.A.3    Meier, E.4    Vinge, M.M.5    Quist, C.6    Petersen, J.S.7
  • 72
    • 40849092954 scopus 로고    scopus 로고
    • Designed modification of partial agonist of ORL1 nociceptin receptor for conversion into highly potent antagonist
    • Li J, Isozaki K, Okada K, Matsushima A, Nose T, Costa T, Shimohigashi Y. Designed modification of partial agonist of ORL1 nociceptin receptor for conversion into highly potent antagonist. Bioorg Med Chem 2008;16:2635-2644.
    • (2008) Bioorg Med Chem , vol.16 , pp. 2635-2644
    • Li, J.1    Isozaki, K.2    Okada, K.3    Matsushima, A.4    Nose, T.5    Costa, T.6    Shimohigashi, Y.7
  • 76
    • 79959542458 scopus 로고    scopus 로고
    • Nociceptin-based analgesics. Patent US 2008/0221304 A1, Synvax Inc.
    • Judd AK. Nociceptin-based analgesics. Patent US 2008/0221304 A1, Synvax Inc. 2008.
    • (2008)
    • Judd, A.K.1
  • 78
    • 79959549482 scopus 로고    scopus 로고
    • Peptide derivatives and medicinal compositions. Patent EP 1275657, Nippon Shinyaku Co. Ltd.
    • Ishiyama K, Tereda T, Oyama T, Ohgi T. Peptide derivatives and medicinal compositions. Patent EP 1275657, Nippon Shinyaku Co. Ltd., 2003.
    • (2003)
    • Ishiyama, K.1    Tereda, T.2    Oyama, T.3    Ohgi, T.4
  • 80
    • 33746795407 scopus 로고    scopus 로고
    • Synthesis and receptor binding properties of chimeric peptides containing a μ-opioid receptor ligand and nociceptin/orphanin FQ receptor ligand Ac-RYYRIK-amide
    • Kawano S, Ambo A, Sasaki Y. Synthesis and receptor binding properties of chimeric peptides containing a μ-opioid receptor ligand and nociceptin/orphanin FQ receptor ligand Ac-RYYRIK-amide. Bioorg Med Chem Lett 2006;16:4839-4841.
    • (2006) Bioorg Med Chem Lett , vol.16 , pp. 4839-4841
    • Kawano, S.1    Ambo, A.2    Sasaki, Y.3
  • 81
    • 34447136763 scopus 로고    scopus 로고
    • Receptor binding properties and antinociceptive effects of chimeric peptides consisting of a μ-opioid receptor agonist and an ORL1 receptor antagonist
    • Kawano S, Ito R, Nishiyama M, Kubo M, Matsushima T, Minamisawa M, Ambo A, Sasaki Y. Receptor binding properties and antinociceptive effects of chimeric peptides consisting of a μ-opioid receptor agonist and an ORL1 receptor antagonist. Biol Pharm Bull 2007;30:1260-1264.
    • (2007) Biol Pharm Bull , vol.30 , pp. 1260-1264
    • Kawano, S.1    Ito, R.2    Nishiyama, M.3    Kubo, M.4    Matsushima, T.5    Minamisawa, M.6    Ambo, A.7    Sasaki, Y.8
  • 82
    • 0030830634 scopus 로고    scopus 로고
    • Comparison of the structure-activity relationships of nociceptin and dynorphin A using chimeric peptides
    • Lapalu S, Moisand C, Marzaguil H, Cambois G, Mollereau C, Meunier JC. Comparison of the structure-activity relationships of nociceptin and dynorphin A using chimeric peptides. FEBS Lett 1997;417:333-336.
    • (1997) FEBS Lett , vol.417 , pp. 333-336
    • Lapalu, S.1    Moisand, C.2    Marzaguil, H.3    Cambois, G.4    Mollereau, C.5    Meunier, J.C.6
  • 85
    • 0037153201 scopus 로고    scopus 로고
    • Probing opioid receptor interactions with azacycloalkane amino acids. Synthesis of a potent and selective ORL1 antagonist
    • Halab L, Becker JA, Darula Z, Tourwé D, Kieffer BL, Simonin F, Lubell WD. Probing opioid receptor interactions with azacycloalkane amino acids. Synthesis of a potent and selective ORL1 antagonist. J Med Chem 2002;45:5353-5357.
    • (2002) J Med Chem , vol.45 , pp. 5353-5357
    • Halab, L.1    Becker, J.A.2    Darula, Z.3    Tourwé, D.4    Kieffer, B.L.5    Simonin, F.6    Lubell, W.D.7
  • 87
    • 0032541091 scopus 로고    scopus 로고
    • Loss of antinociception induced by naloxone benzoylhydrazone in nociceptin receptor-knockout mice
    • Noda Y, Mamiya T, Nabeshima T, Nishi M, Higashioka M, Takeshima H. Loss of antinociception induced by naloxone benzoylhydrazone in nociceptin receptor-knockout mice. J Biol Chem 1998;273:18047-18051.
    • (1998) J Biol Chem , vol.273 , pp. 18047-18051
    • Noda, Y.1    Mamiya, T.2    Nabeshima, T.3    Nishi, M.4    Higashioka, M.5    Takeshima, H.6
  • 88
    • 79959536799 scopus 로고    scopus 로고
    • Morphinan hydroxamic acid compounds. Patent US5834478, Pfizer Inc.
    • Ito F. Morphinan hydroxamic acid compounds. Patent US5834478, Pfizer Inc., 1998.
    • (1998)
    • Ito, F.1
  • 89
  • 91
    • 79959543491 scopus 로고    scopus 로고
    • N-but-3-enyl norbuprenorphine and its use as analgesic. Patent US7125884 B2, Euro-Celtique S.A.
    • Reidenberg BE, Gale DD, Srinivasan VJ. N-but-3-enyl norbuprenorphine and its use as analgesic. Patent US7125884 B2, Euro-Celtique S.A., 2006.
    • (2006)
    • Reidenberg, B.E.1    Gale, D.D.2    Srinivasan, V.J.3
  • 92
    • 79959545377 scopus 로고    scopus 로고
    • Use of morphine derivatives as medicaments for the treatment of neuropathic problems. Patent US6476044 B1, Gruenenthal GmbH
    • Wnendt S, Strassburger W, Buschmann H, Reiss-Mueller E, Krueger T. Use of morphine derivatives as medicaments for the treatment of neuropathic problems. Patent US6476044 B1, Gruenenthal GmbH, 2002.
    • (2002)
    • Wnendt, S.1    Strassburger, W.2    Buschmann, H.3    Reiss-Mueller, E.4    Krueger, T.5
  • 93
    • 0041829500 scopus 로고    scopus 로고
    • Design and parallel synthesis of piperidine libraries targeting the nociceptin (N/OFQ) receptor
    • Chen Z, Miller WS, Shan S, Valenzano KJ. Design and parallel synthesis of piperidine libraries targeting the nociceptin (N/OFQ) receptor. Bioorg Med Chem Lett 2003;13:3247-3252.
    • (2003) Bioorg Med Chem Lett , vol.13 , pp. 3247-3252
    • Chen, Z.1    Miller, W.S.2    Shan, S.3    Valenzano, K.J.4
  • 94
    • 34247866496 scopus 로고    scopus 로고
    • Synthesis and structure-activity relationships of 4-hydroxy-4-phenylpiperidines as nociceptin receptor ligands: Part 1
    • Ho GD, Bercovici A, Tulshian D, Greenlee WJ, Fawzi A, Smith Torhan A, Zhang H. Synthesis and structure-activity relationships of 4-hydroxy-4-phenylpiperidines as nociceptin receptor ligands: Part 1. Bioorg Med Chem Lett 2007;17:3023-3027.
    • (2007) Bioorg Med Chem Lett , vol.17 , pp. 3023-3027
    • Ho, G.D.1    Bercovici, A.2    Tulshian, D.3    Greenlee, W.J.4    Fawzi, A.5    Smith Torhan, A.6    Zhang, H.7
  • 96
    • 79959562032 scopus 로고    scopus 로고
    • Use of 3,4-substituted piperidines. Patent WO 01/32178 A1, Novo Nordisk A/S
    • Thomsen C, Hohlweg R. Use of 3, 4-substituted piperidines. Patent WO 01/32178 A1, Novo Nordisk A/S, 2001.
    • (2001)
    • Thomsen, C.1    Hohlweg, R.2
  • 97
    • 1642498186 scopus 로고    scopus 로고
    • Modification of nociception and morphine tolerance by the selective opiate receptor-like orphan receptor antagonist (-)cis-1-methyl-7-[[4-(2,6-dichlorophenyl)piperidin-1-yl]methyl]-6,7,8,9-tetrahydro-5H-benzocyclohepthen-5-ol (SB-612111)
    • Zaratin PF, Petrone G, Sbacchi M, Garnier M, Fossati C, Petrillo P, Ronzoni S, Giardina GA, Scheideler MA. Modification of nociception and morphine tolerance by the selective opiate receptor-like orphan receptor antagonist (-)cis-1-methyl-7-[[4-(2, 6-dichlorophenyl)piperidin-1-yl]methyl]-6, 7, 8, 9-tetrahydro-5H-benzocyclohepthen-5-ol (SB-612111). J Pharmacol Exp Ther 2004;308:454-461.
    • (2004) J Pharmacol Exp Ther , vol.308 , pp. 454-461
    • Zaratin, P.F.1    Petrone, G.2    Sbacchi, M.3    Garnier, M.4    Fossati, C.5    Petrillo, P.6    Ronzoni, S.7    Giardina, G.A.8    Scheideler, M.A.9
  • 99
    • 34248581615 scopus 로고    scopus 로고
    • Pharmacological characterization of the nociceptin/orphanin FQ receptor antagonist SB-612111 [(-)cis-1-methyl-7-[[4-(2,6-dichlorophenyl)piperidin-1-yl]methyl]-6,7,8,9-tetrahydro-5H-benzocyclohepthen-5-ol]: In vivo studies
    • Rizzi A, Gavioli EC, Marzola G, Spagnolo B, Zucchini S, Ciccocioppo R, Trapella C, Regoli D, Calò G. Pharmacological characterization of the nociceptin/orphanin FQ receptor antagonist SB-612111 [(-)cis-1-methyl-7-[[4-(2, 6-dichlorophenyl)piperidin-1-yl]methyl]-6, 7, 8, 9-tetrahydro-5H-benzocyclohepthen-5-ol]: In vivo studies. J Pharmacol Exp Ther 2007;321:968-974.
    • (2007) J Pharmacol Exp Ther , vol.321 , pp. 968-974
    • Rizzi, A.1    Gavioli, E.C.2    Marzola, G.3    Spagnolo, B.4    Zucchini, S.5    Ciccocioppo, R.6    Trapella, C.7    Regoli, D.8    Calò, G.9
  • 102
    • 79959562656 scopus 로고    scopus 로고
    • 4-Tetrazolyl-4-phenylpiperidine derivatives for treating pain. Patent EP1803718 B1, Euro-Celtique S.A.
    • Chen Z. 4-Tetrazolyl-4-phenylpiperidine derivatives for treating pain. Patent EP1803718 B1, Euro-Celtique S.A., 2008.
    • (2008)
    • Chen, Z.1
  • 104
    • 79959556314 scopus 로고    scopus 로고
    • 8-[bis-(2-chloro-phenyl)-methyl]-3-phenyl-8-azabicyclo[3.2.1]octane-3-carboxylic acid amide as ligand for the nociceptin receptor ORL-1. Patent WO 2007/050719 A1, Schering Co.
    • Sawutz DG, Brianceau P, Bercovici A, Ho GD, Tulshian D. 8-[bis-(2-chloro-phenyl)-methyl]-3-phenyl-8-azabicyclo[3.2.1]octane-3-carboxylic acid amide as ligand for the nociceptin receptor ORL-1. Patent WO 2007/050719 A1, Schering Co., 2007.
    • (2007)
    • Sawutz, D.G.1    Brianceau, P.2    Bercovici, A.3    Ho, G.D.4    Tulshian, D.5
  • 105
  • 106
    • 56249092056 scopus 로고    scopus 로고
    • Structure-activity relationship of 3-substituted N-benzhydryl-nortropane analogs as nociceptin receptor ligands for the treatment of cough
    • Yang SW, Ho G, Tulshian D, Greenlee WJ, Fernandez X, McLeod RL, Eckel S, Anthes J. Structure-activity relationship of 3-substituted N-benzhydryl-nortropane analogs as nociceptin receptor ligands for the treatment of cough. Bioorg Med Chem Lett 2008;18:6340-6343.
    • (2008) Bioorg Med Chem Lett , vol.18 , pp. 6340-6343
    • Yang, S.W.1    Ho, G.2    Tulshian, D.3    Greenlee, W.J.4    Fernandez, X.5    McLeod, R.L.6    Eckel, S.7    Anthes, J.8
  • 110
    • 0033576679 scopus 로고    scopus 로고
    • Discovery of the first potent and selective small molecule opioid receptor-like (ORL1) antagonist: 1-[(3R,4R)]-1-cyclooctylmethyl-3-hydroxymethyl-4-piperidyl]-3-ethyl-1,3-dihydro-2H-benzimidazol-2-one (J-113397)
    • Kawamoto H, Ozaki S, Itoh Y, Miyaji M, Arai S, Nakashima H, Kato T, Ohta H, Iwasawa Y. Discovery of the first potent and selective small molecule opioid receptor-like (ORL1) antagonist: 1-[(3R, 4R)]-1-cyclooctylmethyl-3-hydroxymethyl-4-piperidyl]-3-ethyl-1, 3-dihydro-2H-benzimidazol-2-one (J-113397). J Med Chem 1999;42:5061-5063.
    • (1999) J Med Chem , vol.42 , pp. 5061-5063
    • Kawamoto, H.1    Ozaki, S.2    Itoh, Y.3    Miyaji, M.4    Arai, S.5    Nakashima, H.6    Kato, T.7    Ohta, H.8    Iwasawa, Y.9
  • 113
    • 0034944564 scopus 로고    scopus 로고
    • A new synthetic approach to 1-[(3R,4R)]-1-cyclooctylmethyl-3-hydroxymethyl-4-piperidyl]-3-ethyl-1,3-dihydro-2H-benzimidazol-2-one (J-113397), the first non-peptide ORL-1 receptor antagonist
    • De Risi C, Pollini GP, Trapella C, Peretto I, Ronzoni S, Giardina GAM. A new synthetic approach to 1-[(3R, 4R)]-1-cyclooctylmethyl-3-hydroxymethyl-4-piperidyl]-3-ethyl-1, 3-dihydro-2H-benzimidazol-2-one (J-113397), the first non-peptide ORL-1 receptor antagonist. Bioorg Med Chem 2001;9:1871-1877.
    • (2001) Bioorg Med Chem , vol.9 , pp. 1871-1877
    • De Risi, C.1    Pollini, G.P.2    Trapella, C.3    Peretto, I.4    Ronzoni, S.5    Giardina, G.A.M.6
  • 114
    • 38549171441 scopus 로고    scopus 로고
    • A new synthesis of the ORL-1 antagonist 1-[(3R,4R)]-1-cyclooctylmethyl-3-hydroxymethyl-4-piperidyl]-3-ethyl-1,3-dihydro-2H-benzimidazol-2-one (J-113397) and activity in a calcium mobilization assay
    • Smith ED, Vinson NA, Zhong D, Berrang BD, Catanzaro JL, Thomas JB, Navarro HA, Gilmour BP, Deschamps J, Carroll FI. A new synthesis of the ORL-1 antagonist 1-[(3R, 4R)]-1-cyclooctylmethyl-3-hydroxymethyl-4-piperidyl]-3-ethyl-1, 3-dihydro-2H-benzimidazol-2-one (J-113397) and activity in a calcium mobilization assay. Bioorg Med Chem 2008;16:822-829.
    • (2008) Bioorg Med Chem , vol.16 , pp. 822-829
    • Smith, E.D.1    Vinson, N.A.2    Zhong, D.3    Berrang, B.D.4    Catanzaro, J.L.5    Thomas, J.B.6    Navarro, H.A.7    Gilmour, B.P.8    Deschamps, J.9    Carroll, F.I.10
  • 117
    • 79959571957 scopus 로고    scopus 로고
    • Benzimidazole compounds having nociceptin receptor affinity. Patent US7456198 B2, Purdue Pharma L.P.
    • Kyle D, Goehring RR, Shao B. Benzimidazole compounds having nociceptin receptor affinity. Patent US7456198 B2, Purdue Pharma L.P., 2008.
    • (2008)
    • Kyle, D.1    Goehring, R.R.2    Shao, B.3
  • 119
    • 79959556701 scopus 로고    scopus 로고
    • N-dihydroxyalkyl-substituted 2-oxo-imidazole derivative. Patent EP 1914232, Banyu Pharmaceutical Co. Ltd.
    • Hashimoto M, Iwasawa Y, Kawamoto H, Ohta H, Ozaki S, Sagara T, Sakoh H, Satoh A. N-dihydroxyalkyl-substituted 2-oxo-imidazole derivative. Patent EP 1914232, Banyu Pharmaceutical Co. Ltd., 2008.
    • (2008)
    • Hashimoto, M.1    Iwasawa, Y.2    Kawamoto, H.3    Ohta, H.4    Ozaki, S.5    Sagara, T.6    Sakoh, H.7    Satoh, A.8
  • 120
    • 79959564741 scopus 로고    scopus 로고
    • 4-(2-Keto-1-benzimidazolinyl)piperidine compounds as ORL1-receptor agonists. Patent WO/1999/036421, Pfizer Inc.
    • Ito F, Kondo H, Noguchi H, Ohashi Y, Yamagishi T. 4-(2-Keto-1-benzimidazolinyl)piperidine compounds as ORL1-receptor agonists. Patent WO/1999/036421, Pfizer Inc., 1999.
    • (1999)
    • Ito, F.1    Kondo, H.2    Noguchi, H.3    Ohashi, Y.4    Yamagishi, T.5
  • 122
    • 33847794821 scopus 로고    scopus 로고
    • Synthesis and evaluation of N-3 substituted phenoxypropyl piperidine benzimidazol-2-one analogues as NOP receptor agonists with analgesic and sedative properties
    • Palin R, Bom A, Clark JK, Evans L, Feilden H, Houghton AK, Jones PS, Montgomery B, Weston MA, Wishart G. Synthesis and evaluation of N-3 substituted phenoxypropyl piperidine benzimidazol-2-one analogues as NOP receptor agonists with analgesic and sedative properties. Bioorg Med Chem 2007;15:1828-1847.
    • (2007) Bioorg Med Chem , vol.15 , pp. 1828-1847
    • Palin, R.1    Bom, A.2    Clark, J.K.3    Evans, L.4    Feilden, H.5    Houghton, A.K.6    Jones, P.S.7    Montgomery, B.8    Weston, M.A.9    Wishart, G.10
  • 123
    • 40949083023 scopus 로고    scopus 로고
    • Structure-activity relationships and CoMFA of N-3 substituted phenoxypropyl piperidine benzimidazol-2-one analogues as NOP receptor agonists with analgesic properties
    • Palin R, Clark JK, Evans L, Houghton AK, Jones PS, Prosser A, Wishart G, Yoshiizumi K. Structure-activity relationships and CoMFA of N-3 substituted phenoxypropyl piperidine benzimidazol-2-one analogues as NOP receptor agonists with analgesic properties. Bioorg Med Chem 2008;16:2829-2851.
    • (2008) Bioorg Med Chem , vol.16 , pp. 2829-2851
    • Palin, R.1    Clark, J.K.2    Evans, L.3    Houghton, A.K.4    Jones, P.S.5    Prosser, A.6    Wishart, G.7    Yoshiizumi, K.8
  • 124
    • 79959535510 scopus 로고    scopus 로고
    • Agent for prophylaxis or treatment of alcohol dependence or drug dependence. Patent WO/2008/050698, Mitsubishi Tanabe Pharma Co.
    • Teshima K, Ciccocioppo R, Massi M. Agent for prophylaxis or treatment of alcohol dependence or drug dependence. Patent WO/2008/050698, Mitsubishi Tanabe Pharma Co., 2008.
    • (2008)
    • Teshima, K.1    Ciccocioppo, R.2    Massi, M.3
  • 125
    • 28444485374 scopus 로고    scopus 로고
    • Nonphotic entrainment of the circadian body temperature rhythm by the selective ORL1 receptor agonist W-212393 in rats
    • Teshima K, Minoguchi M, Tounai S, Ashimori A, Eguchi J, Allen CN, Shibata S. Nonphotic entrainment of the circadian body temperature rhythm by the selective ORL1 receptor agonist W-212393 in rats. Br J Pharmacol 2005;146:33-40.
    • (2005) Br J Pharmacol , vol.146 , pp. 33-40
    • Teshima, K.1    Minoguchi, M.2    Tounai, S.3    Ashimori, A.4    Eguchi, J.5    Allen, C.N.6    Shibata, S.7
  • 126
    • 0346887162 scopus 로고    scopus 로고
    • The design and synthesis of a novel quinolizidine template for potent opioid and opioid receptor-like (ORL1, NOP) receptor ligands
    • Jong L, Zaveri N, Toll L. The design and synthesis of a novel quinolizidine template for potent opioid and opioid receptor-like (ORL1, NOP) receptor ligands. Bioorg Med Chem Lett 2004;14:181-185.
    • (2004) Bioorg Med Chem Lett , vol.14 , pp. 181-185
    • Jong, L.1    Zaveri, N.2    Toll, L.3
  • 127
    • 1242293874 scopus 로고    scopus 로고
    • Design and synthesis of novel small molecule N/OFQ receptor antagonists
    • Chen Z, Goehring RR, Valenzano KJ, Kyle DJ. Design and synthesis of novel small molecule N/OFQ receptor antagonists. Bioorg Med Chem Lett 2004;14:1347-1351.
    • (2004) Bioorg Med Chem Lett , vol.14 , pp. 1347-1351
    • Chen, Z.1    Goehring, R.R.2    Valenzano, K.J.3    Kyle, D.J.4
  • 128
    • 79959569426 scopus 로고    scopus 로고
    • Octahydrobenzimidazolone compounds as analgetics. Patent EP1975164 A2, Euro-Celtique S.A.
    • Goehring RR, Chen Z, Kyle D, Victory S. Octahydrobenzimidazolone compounds as analgetics. Patent EP1975164 A2, Euro-Celtique S.A., 2008.
    • (2008)
    • Goehring, R.R.1    Chen, Z.2    Kyle, D.3    Victory, S.4
  • 129
    • 41549119871 scopus 로고    scopus 로고
    • Pharmacological characterization of the newly syntesized nociceptin/orphanin FQ receptor agonist 1-[1-(1-methylcyclooctyl)-4-piperidinyl]-2-[(3R)-3-piperidinyl]-1H-benzimidazole as an anxyolitic agent
    • Hirao A, Imai A, Sugie Y, Yamada Y, Hayashi S, Toide K. Pharmacological characterization of the newly syntesized nociceptin/orphanin FQ receptor agonist 1-[1-(1-methylcyclooctyl)-4-piperidinyl]-2-[(3R)-3-piperidinyl]-1H-benzimidazole as an anxyolitic agent. J Pharmacol Sci 2008;106:361-368.
    • (2008) J Pharmacol Sci , vol.106 , pp. 361-368
    • Hirao, A.1    Imai, A.2    Sugie, Y.3    Yamada, Y.4    Hayashi, S.5    Toide, K.6
  • 130
    • 61449229868 scopus 로고    scopus 로고
    • Novel non-peptide nociceptin/orphanin FQ receptor agonist 1-[1-(1-methylcyclooctyl)-4-piperidinyl]-2-[(3R)-3-piperidinyl]-1H-benzimidazole: Design, synthesis and structure-activity relationship of oral receptor occupancy in the brain for orally potent antianxiety drug
    • Hayashi S, Hirao A, Imai A, Nakamura H, Murata Y, Ohashi K, Nakata E. Novel non-peptide nociceptin/orphanin FQ receptor agonist 1-[1-(1-methylcyclooctyl)-4-piperidinyl]-2-[(3R)-3-piperidinyl]-1H-benzimidazole: Design, synthesis and structure-activity relationship of oral receptor occupancy in the brain for orally potent antianxiety drug. J Med Chem 2009;52:610-625.
    • (2009) J Med Chem , vol.52 , pp. 610-625
    • Hayashi, S.1    Hirao, A.2    Imai, A.3    Nakamura, H.4    Murata, Y.5    Ohashi, K.6    Nakata, E.7
  • 131
    • 37549001046 scopus 로고    scopus 로고
    • Pharmacological properties of a novel nociceptin/orphanin FQ receptor agonist, 2-(3,5-dimethylpiperazin-1-yl)-1-[1-(1-methylcyclooctyl)piperidin-4-yl]-1H-benzimidazole, with anxiolytic potential
    • Hirao A, Imai A, Sugie Y, Tamura T, Shimokawa H, Toide K. Pharmacological properties of a novel nociceptin/orphanin FQ receptor agonist, 2-(3, 5-dimethylpiperazin-1-yl)-1-[1-(1-methylcyclooctyl)piperidin-4-yl]-1H-benzimidazole, with anxiolytic potential. Eur J Pharmacol 2008;579:189-195.
    • (2008) Eur J Pharmacol , vol.579 , pp. 189-195
    • Hirao, A.1    Imai, A.2    Sugie, Y.3    Tamura, T.4    Shimokawa, H.5    Toide, K.6
  • 132
    • 2542609191 scopus 로고    scopus 로고
    • A novel series of piperidin-4-yl-1,3-dihydroindol-2-ones as agonist and antagonist ligands at the nociceptin receptor
    • Zaveri NT, Jiang F, Olsen CM, Deschamps JR, Parrish D, Polgar W, Toll L. A novel series of piperidin-4-yl-1, 3-dihydroindol-2-ones as agonist and antagonist ligands at the nociceptin receptor. J Med Chem 2004;47:2973-2976.
    • (2004) J Med Chem , vol.47 , pp. 2973-2976
    • Zaveri, N.T.1    Jiang, F.2    Olsen, C.M.3    Deschamps, J.R.4    Parrish, D.5    Polgar, W.6    Toll, L.7
  • 133
    • 33846461154 scopus 로고    scopus 로고
    • SR 16435 [1-(1-bicyclo[3.3.1]nonan-9-yl)piperidin-4-yl)indolin-2-one], a novel mixed nociceptin/orphanin FQ/μ-opioid receptor partial agonist: Analgesic and rewarding properties in mice
    • Khroyan TV, Zaveri NT, Polgar WE, Orduna J, Olsen C, Jiang F, Toll L. SR 16435 [1-(1-bicyclo[3.3.1]nonan-9-yl)piperidin-4-yl)indolin-2-one], a novel mixed nociceptin/orphanin FQ/μ-opioid receptor partial agonist: Analgesic and rewarding properties in mice. J Pharmacol Exp Ther 2007;320:934-943.
    • (2007) J Pharmacol Exp Ther , vol.320 , pp. 934-943
    • Khroyan, T.V.1    Zaveri, N.T.2    Polgar, W.E.3    Orduna, J.4    Olsen, C.5    Jiang, F.6    Toll, L.7
  • 134
    • 30544437362 scopus 로고    scopus 로고
    • Small-molecule agonists and antagonists of the opioid receptor-like receptor (ORL1, NOP): Ligand-based analysis of structural factors influencing intrinsic activity at NOP
    • Zaveri N, Yiang F, Olsen C, Polgar W, Toll L. Small-molecule agonists and antagonists of the opioid receptor-like receptor (ORL1, NOP): Ligand-based analysis of structural factors influencing intrinsic activity at NOP. AAPS J 2005;7:E345-E352.
    • (2005) AAPS J , vol.7
    • Zaveri, N.1    Yiang, F.2    Olsen, C.3    Polgar, W.4    Toll, L.5
  • 138
    • 79959558452 scopus 로고    scopus 로고
    • Heterocyclic-substituted piperidine as ORL-1 ligands. Patent WO/2008/089201, Purdue Pharma L.P.and Shionogi & Co.Ltd
    • Baba Y, Brown KC, Goehring RR, Tsuno N. Heterocyclic-substituted piperidine as ORL-1 ligands. Patent WO/2008/089201, Purdue Pharma L.P.and Shionogi & Co.Ltd, 2008.
    • (2008)
    • Baba, Y.1    Brown, K.C.2    Goehring, R.R.3    Tsuno, N.4
  • 139
    • 79959555645 scopus 로고    scopus 로고
    • 1-(4-Piperidinyl)-1,3-dihydro-2H-benzoxazole-2-one derivatives and related compounds as nociceptin analogs and ORL1 ligands for the treatment of pain. Patent EP1598340 B1, Euro-Celtique S.A.
    • Sun Q, Goehring RR, Kyle D, Chen Z, Victory S, Whitehead J. 1-(4-Piperidinyl)-1, 3-dihydro-2H-benzoxazole-2-one derivatives and related compounds as nociceptin analogs and ORL1 ligands for the treatment of pain. Patent EP1598340 B1, Euro-Celtique S.A., 2009.
    • (2009)
    • Sun, Q.1    Goehring, R.R.2    Kyle, D.3    Chen, Z.4    Victory, S.5    Whitehead, J.6
  • 141
    • 79959566575 scopus 로고    scopus 로고
    • 4-Oxadiazolyl-piperidine compounds and use thereof. Patent US 2008/0319020; Purdue Pharma L.P.
    • Tafesse L. 4-Oxadiazolyl-piperidine compounds and use thereof. Patent US 2008/0319020; Purdue Pharma L.P., 2008.
    • (2008)
    • Tafesse, L.1
  • 143
    • 0033575662 scopus 로고    scopus 로고
    • 8-Acenaphthen-1-yl-1-phenyl-1,3,8-triaza-spiro[4.5]decan-4-one derivatives as orphanin FQ receptor agonists
    • Wichmann J, Adam G, Röver S, Cesura AM, Dautzenberg FM, Jenck F. 8-Acenaphthen-1-yl-1-phenyl-1, 3, 8-triaza-spiro[4.5]decan-4-one derivatives as orphanin FQ receptor agonists. Bioorg Med Chem Lett 1999;9:2343-2348.
    • (1999) Bioorg Med Chem Lett , vol.9 , pp. 2343-2348
    • Wichmann, J.1    Adam, G.2    Röver, S.3    Cesura, A.M.4    Dautzenberg, F.M.5    Jenck, F.6
  • 144
    • 0342313481 scopus 로고    scopus 로고
    • ORL1 receptor ligands: Structure-activity relationships of 8-cycloalkyl-1-phenyl-1,3,8-triaza-spiro[4.5]decan-4-ones
    • Röver S, Wichmann J, Jenck F, Adam G, Cesura AM. ORL1 receptor ligands: Structure-activity relationships of 8-cycloalkyl-1-phenyl-1, 3, 8-triaza-spiro[4.5]decan-4-ones. Bioorg Med Chem Lett 2000;10:831-834.
    • (2000) Bioorg Med Chem Lett , vol.10 , pp. 831-834
    • Röver, S.1    Wichmann, J.2    Jenck, F.3    Adam, G.4    Cesura, A.M.5
  • 145
    • 0033818484 scopus 로고    scopus 로고
    • Synthesis of (1S,3aS)-8-(2,3,3a,4,5,6-hexahydro-1H-phenalen-1-yl)-1-phenyl-1,3,8-triazaspiro[4.5]decan-4-one, a potent and selective orphanin FQ (OFQ) receptor agonist with anxiolytic-like properties
    • Wichmann J, Adam G, Röver S, Hennig M, Scalone M, Cesura AM, Dautzenberg FM, Jenck F. Synthesis of (1S, 3aS)-8-(2, 3, 3a, 4, 5, 6-hexahydro-1H-phenalen-1-yl)-1-phenyl-1, 3, 8-triazaspiro[4.5]decan-4-one, a potent and selective orphanin FQ (OFQ) receptor agonist with anxiolytic-like properties. Eur J Med Chem 2000;35:839-851.
    • (2000) Eur J Med Chem , vol.35 , pp. 839-851
    • Wichmann, J.1    Adam, G.2    Röver, S.3    Hennig, M.4    Scalone, M.5    Cesura, A.M.6    Dautzenberg, F.M.7    Jenck, F.8
  • 146
    • 34247866273 scopus 로고    scopus 로고
    • The pharmacology of Ro 64-6198, a systemically active, nonpeptide NOP receptor (opiate receptor-like 1, ORL-1) agonist with diverse preclinical therapeutic activity
    • Schoblock JR. The pharmacology of Ro 64-6198, a systemically active, nonpeptide NOP receptor (opiate receptor-like 1, ORL-1) agonist with diverse preclinical therapeutic activity. CNS Drug Rev 2007;13:107-136.
    • (2007) CNS Drug Rev , vol.13 , pp. 107-136
    • Schoblock, J.R.1
  • 149
    • 0033709561 scopus 로고    scopus 로고
    • 8-Naphthalen-1-ylmethyl-4-oxo-1-phenyl-1,3,8-triaza-spiro[4.5]dec-3-yl)acetic acid methyl ester (NNC 63-0532) is a novel potent nociceptin receptor agonist
    • Thomsen C, Hohlweg R. (8-Naphthalen-1-ylmethyl-4-oxo-1-phenyl-1, 3, 8-triaza-spiro[4.5]dec-3-yl)acetic acid methyl ester (NNC 63-0532) is a novel potent nociceptin receptor agonist. Br J Pharmacol 2000;131:903-908.
    • (2000) Br J Pharmacol , vol.131 , pp. 903-908
    • Thomsen, C.1    Hohlweg, R.2
  • 150
    • 79959563281 scopus 로고    scopus 로고
    • Novel triazaspirodecanones with high affinity for opioid receptor subtypes. Patent WO/2001/036418, Novo Nordisk A/s
    • Hohlweg R, Watson B, Pettersson I. Novel triazaspirodecanones with high affinity for opioid receptor subtypes. Patent WO/2001/036418, Novo Nordisk A/s, 2001.
    • (2001)
    • Hohlweg, R.1    Watson, B.2    Pettersson, I.3
  • 151
    • 79959568631 scopus 로고    scopus 로고
    • 1,3,8-Triazaspiro[4,5]decanone compounds as orl-1 receptor agonists. Patent EP0997464, Pfizer Inc.
    • Ito F, Ohashi Y. 1, 3, 8-Triazaspiro[4, 5]decanone compounds as orl-1 receptor agonists. Patent EP0997464, Pfizer Inc., 2005.
    • (2005)
    • Ito, F.1    Ohashi, Y.2
  • 152
    • 79959560777 scopus 로고    scopus 로고
    • 4-oxoimidazolidine-5-spiro-nitrogen containing heterocyclic compound. Patent JP 2000169476, Banyu Pharmaceutical Co.
    • Kawamoto H, Ozaki S, Ito Y, Iwazawa Z. 4-oxoimidazolidine-5-spiro-nitrogen containing heterocyclic compound. Patent JP 2000169476, Banyu Pharmaceutical Co., 2000.
    • (2000)
    • Kawamoto, H.1    Ozaki, S.2    Ito, Y.3    Iwazawa, Z.4
  • 153
    • 79959564129 scopus 로고    scopus 로고
    • Hydroxy alkyl substituted 1,3,8-triazaspiro[4.5]decan-4-one derivatives useful for the treatment of ORL-1 receptor mediated disorders. Patent US2009/0124614, Johnson & Johnson
    • Battista K, Bignan G, Connolly PJ, Reitz AB, Ross TM, Scott M, Middleton SA, Orsini M. Hydroxy alkyl substituted 1, 3, 8-triazaspiro[4.5]decan-4-one derivatives useful for the treatment of ORL-1 receptor mediated disorders. Patent US2009/0124614, Johnson & Johnson, 2009.
    • (2009)
    • Battista, K.1    Bignan, G.2    Connolly, P.J.3    Reitz, A.B.4    Ross, T.M.5    Scott, M.6    Middleton, S.A.7    Orsini, M.8
  • 155
    • 33947585045 scopus 로고    scopus 로고
    • Synthesis and structure-activity relationships of N-substituted spiropiperidines as nociceptin receptor ligands
    • Caldwell JP, Matasi JJ, Zhang H, Fawzi A, Tulshian DB. Synthesis and structure-activity relationships of N-substituted spiropiperidines as nociceptin receptor ligands. Bioorg Med Chem Lett 2007;17:2281-2284.
    • (2007) Bioorg Med Chem Lett , vol.17 , pp. 2281-2284
    • Caldwell, J.P.1    Matasi, J.J.2    Zhang, H.3    Fawzi, A.4    Tulshian, D.B.5
  • 156
  • 157
    • 79959565580 scopus 로고    scopus 로고
    • Triazaspiro compounds useful for treating or preventing pain. Patent US7414062, Purdue Pharma L.P.
    • Chen Z, Victory S. Triazaspiro compounds useful for treating or preventing pain. Patent US7414062, Purdue Pharma L.P., 2008.
    • (2008)
    • Chen, Z.1    Victory, S.2
  • 158
    • 79959539954 scopus 로고    scopus 로고
    • 1,3,8-trisubstituted-1,3,8-triaza-spiro[4.5]decan-4-one derivatives as ligands of the ORL-1 receptor. Patent US2008/0249122, Johnson & Johnson
    • Bignan GC, Hlasta DJ, Ryan RR. 1, 3, 8-trisubstituted-1, 3, 8-triaza-spiro[4.5]decan-4-one derivatives as ligands of the ORL-1 receptor. Patent US2008/0249122, Johnson & Johnson, 2008.
    • (2008)
    • Bignan, G.C.1    Hlasta, D.J.2    Ryan, R.R.3
  • 159
    • 79959549053 scopus 로고    scopus 로고
    • Nociceptin analogues and uses thereof. Patent US20080287478 A1, Clark & Elbing LLP
    • Hansen LBL, Larsen BD, Thorkildsen C, Knudsen CB. Nociceptin analogues and uses thereof. Patent US20080287478 A1, Clark & Elbing LLP, 2008.
    • (2008)
    • Hansen, L.B.L.1    Larsen, B.D.2    Thorkildsen, C.3    Knudsen, C.B.4
  • 160
    • 3042687618 scopus 로고    scopus 로고
    • Nonpeptide/peptide chimeric ligands for the nociceptin/orphanin FQ receptor: Design, synthesis and in vitro pharmacological activity
    • Guerrini R, Carrà G, Calò G, Trapella C, Marzola E, Rizzi D, Regoli D, Salvadori S. Nonpeptide/peptide chimeric ligands for the nociceptin/orphanin FQ receptor: Design, synthesis and in vitro pharmacological activity. J Pept Res 2004;63:477-484.
    • (2004) J Pept Res , vol.63 , pp. 477-484
    • Guerrini, R.1    Carrà, G.2    Calò, G.3    Trapella, C.4    Marzola, E.5    Rizzi, D.6    Regoli, D.7    Salvadori, S.8
  • 161
    • 79959570980 scopus 로고    scopus 로고
    • 4-oxoimidazolidine-2-spiro-nitrogenous heterocycle compounds. Patent WO/2001/96337, Banyu Pharmaceutical Co.
    • Satoh A, Kato T, Ooi N, Iwasawa Y. 4-oxoimidazolidine-2-spiro-nitrogenous heterocycle compounds. Patent WO/2001/96337, Banyu Pharmaceutical Co., 2001.
    • (2001)
    • Satoh, A.1    Kato, T.2    Ooi, N.3    Iwasawa, Y.4
  • 162
    • 79959557827 scopus 로고    scopus 로고
    • 4-oxoimidazolidine-2-spiropiperidine derivative. Patent EP1420020, Banyu Pharmaceutical Co.
    • Hashimoto M, Okamoto O, Ozaki S, Ohta H. 4-oxoimidazolidine-2-spiropiperidine derivative. Patent EP1420020, Banyu Pharmaceutical Co., 2008.
    • (2008)
    • Hashimoto, M.1    Okamoto, O.2    Ozaki, S.3    Ohta, H.4
  • 167
    • 44849137530 scopus 로고    scopus 로고
    • Design, synthesis, and structure-activity relationship study of a novel class of ORL1 receptor antagonists based on N-biarylmethylspiropiperidine
    • Yoshizumi T, Miyazoe H, Ito H, Tsujita T, Takahashi H, Asai M, Ozaki S, Ohta H, Okamoto O. Design, synthesis, and structure-activity relationship study of a novel class of ORL1 receptor antagonists based on N-biarylmethylspiropiperidine. Bioorg Med Chem Lett 2008;18:3778-3782.
    • (2008) Bioorg Med Chem Lett , vol.18 , pp. 3778-3782
    • Yoshizumi, T.1    Miyazoe, H.2    Ito, H.3    Tsujita, T.4    Takahashi, H.5    Asai, M.6    Ozaki, S.7    Ohta, H.8    Okamoto, O.9
  • 168
    • 79959555238 scopus 로고    scopus 로고
    • Spiroindene and spiroindane compounds. EP 2033644, Euro-Celtique S.A.
    • Goehring RR, Kyle DJ, Victory SF. Spiroindene and spiroindane compounds. EP 2033644, Euro-Celtique S.A., 2009.
    • (2009)
    • Goehring, R.R.1    Kyle, D.J.2    Victory, S.F.3
  • 170
    • 79959562459 scopus 로고    scopus 로고
    • Novel 3-spirocyclic indolyl derivatives useful as ORL-1 receptor modulators. Patent US 2007/0112016, Johnson & Johnson
    • Battista KA, Bignan GC, Connolly PJ, Liu JJ, Middleton SA, Orsini MJ. Novel 3-spirocyclic indolyl derivatives useful as ORL-1 receptor modulators. Patent US 2007/0112016, Johnson & Johnson, 2007.
    • (2007)
    • Battista, K.A.1    Bignan, G.C.2    Connolly, P.J.3    Liu, J.J.4    Middleton, S.A.5    Orsini, M.J.6
  • 172
    • 39749191240 scopus 로고    scopus 로고
    • Synthesis and pharmacological evaluation of 1,2-dihydrospiro[isoquinoline-4(3H),4'-piperidin]-3-ones as nociceptin receptor agonists
    • Mustazza C, Borioni A, Sestili I, Sbraccia M, Rodomonte A, Del Giudice MR. Synthesis and pharmacological evaluation of 1, 2-dihydrospiro[isoquinoline-4(3H), 4'-piperidin]-3-ones as nociceptin receptor agonists. J Med Chem 2008;51:1058-1062.
    • (2008) J Med Chem , vol.51 , pp. 1058-1062
    • Mustazza, C.1    Borioni, A.2    Sestili, I.3    Sbraccia, M.4    Rodomonte, A.5    Del Giudice, M.R.6
  • 173
    • 33646416774 scopus 로고    scopus 로고
    • Synthesis and evaluation as NOP ligands of some spiro[piperidine-4,2'(1'H)-quinazolin]-4'(3'H)-ones and spiro[piperidine-4,5'(6'H)-[1,2,4]triazolo[1,5-c]quinazolines]
    • Mustazza C, Borioni A, Sestili I, Sbraccia M, Rodomonte A, Ferretti R, Del Giudice MR. Synthesis and evaluation as NOP ligands of some spiro[piperidine-4, 2'(1'H)-quinazolin]-4'(3'H)-ones and spiro[piperidine-4, 5'(6'H)-[1, 2, 4]triazolo[1, 5-c]quinazolines]. Chem Pharm Bull (Tokyo) 2006;54:611-622.
    • (2006) Chem Pharm Bull (Tokyo) , vol.54 , pp. 611-622
    • Mustazza, C.1    Borioni, A.2    Sestili, I.3    Sbraccia, M.4    Rodomonte, A.5    Ferretti, R.6    Del Giudice, M.R.7
  • 174
    • 79959536341 scopus 로고    scopus 로고
    • Alpha aryl or heteroaryl methyl beta piperidino propanamide compounds as ORL1 receptor antagonists. Patent US7354925, Pfizer Inc.
    • Hashizume Y, Hirota M, Mihara S, Nakamura H, Koike H, Matsumoto Y. Alpha aryl or heteroaryl methyl beta piperidino propanamide compounds as ORL1 receptor antagonists. Patent US7354925, Pfizer Inc., 2008.
    • (2008)
    • Hashizume, Y.1    Hirota, M.2    Mihara, S.3    Nakamura, H.4    Koike, H.5    Matsumoto, Y.6
  • 175
    • 79959572379 scopus 로고    scopus 로고
    • Alpha-(aryl- or heteroaryl-methyl)-beta-piperidinopropanoic acid compounds as Orl-1 receptor antagonists. Patent US20080207665, Pfizer Inc.
    • Hashizume Y, Hirota M, Mihara S, Nakamura H, Koike H, Matsumoto Y. Alpha-(aryl- or heteroaryl-methyl)-beta-piperidinopropanoic acid compounds as Orl-1 receptor antagonists. Patent US20080207665, Pfizer Inc., 2008.
    • (2008)
    • Hashizume, Y.1    Hirota, M.2    Mihara, S.3    Nakamura, H.4    Koike, H.5    Matsumoto, Y.6
  • 176
    • 79959560776 scopus 로고    scopus 로고
    • Alpha (aryl- or heteroaryl-methyl)-beta-piperidino propanamide compounds as Orl-1 receptor antagonists, Patent US20080200490, Pfizer Inc.
    • Hashizume Y, Hirota M, Mihara S, Nakamura H, Koike H, Matsumoto Y. Alpha (aryl- or heteroaryl-methyl)-beta-piperidino propanamide compounds as Orl-1 receptor antagonists, Patent US20080200490, Pfizer Inc., 2008.
    • (2008)
    • Hashizume, Y.1    Hirota, M.2    Mihara, S.3    Nakamura, H.4    Koike, H.5    Matsumoto, Y.6
  • 177
    • 0034736150 scopus 로고    scopus 로고
    • 4-Aminoquinolines: Novel nociceptin antagonists with analgesic activity
    • Shinkai H, Ito T, Iida T, Kitao Y, Yamada H, Uchida I. 4-Aminoquinolines: Novel nociceptin antagonists with analgesic activity. J Med Chem 2000;43:4667-4677.
    • (2000) J Med Chem , vol.43 , pp. 4667-4677
    • Shinkai, H.1    Ito, T.2    Iida, T.3    Kitao, Y.4    Yamada, H.5    Uchida, I.6
  • 179
    • 84962343524 scopus 로고    scopus 로고
    • A new synthetic approach of N-(4-amino-2-methylquinolin-6-yl)-2-(4-ethylphenoxymethyl)benzamide (JTC-801) and its analogues and their pharmacological evaluation as nociceptin receptor (NOP) antagonists
    • Sestili I, Borioni A, Mustazza C, Rodomonte A, Turchetto L, Sbraccia M, Riitano D, Del Giudice MR. A new synthetic approach of N-(4-amino-2-methylquinolin-6-yl)-2-(4-ethylphenoxymethyl)benzamide (JTC-801) and its analogues and their pharmacological evaluation as nociceptin receptor (NOP) antagonists. Eur J Med Chem 2004;39:1047-1057.
    • (2004) Eur J Med Chem , vol.39 , pp. 1047-1057
    • Sestili, I.1    Borioni, A.2    Mustazza, C.3    Rodomonte, A.4    Turchetto, L.5    Sbraccia, M.6    Riitano, D.7    Del Giudice, M.R.8
  • 180
    • 79959562654 scopus 로고    scopus 로고
    • Amide derivatives and nociceptin antagonists. Patent US20060030565; Japan Tobacco Inc.
    • Shinkai H, Ito T, Yamada H. Amide derivatives and nociceptin antagonists. Patent US20060030565; Japan Tobacco Inc., 2006.
    • (2006)
    • Shinkai, H.1    Ito, T.2    Yamada, H.3
  • 181
    • 79959554414 scopus 로고    scopus 로고
    • Antipruritics. Patent US20080103163, Dreier LLP
    • Oyama T, Sakano K. Antipruritics. Patent US20080103163, Dreier LLP, 2008.
    • (2008)
    • Oyama, T.1    Sakano, K.2
  • 182
    • 79959535711 scopus 로고    scopus 로고
    • Quinazoline derivatives and drugs. Patent EP1340748, Nippon Shinyaku Co. Ltd.
    • Okano M, Mori K. Quinazoline derivatives and drugs. Patent EP1340748, Nippon Shinyaku Co. Ltd., 2008.
    • (2008)
    • Okano, M.1    Mori, K.2
  • 183
    • 57649183705 scopus 로고    scopus 로고
    • Discovery and structure-activity relationships of 4-aminoquinazoline derivatives, a novel class of opioid receptor-like 1 (ORL1) antagonists
    • Okano M, Mito J, Maruyama Y, Masuda H, Niwa T, Nakagawa S, Nakamura Y, Matsuura A. Discovery and structure-activity relationships of 4-aminoquinazoline derivatives, a novel class of opioid receptor-like 1 (ORL1) antagonists. Bioorg Med Chem 2009;17:119-132.
    • (2009) Bioorg Med Chem , vol.17 , pp. 119-132
    • Okano, M.1    Mito, J.2    Maruyama, Y.3    Masuda, H.4    Niwa, T.5    Nakagawa, S.6    Nakamura, Y.7    Matsuura, A.8
  • 186
    • 33646849246 scopus 로고    scopus 로고
    • Design, synthesis and biological evaluation of indole derivatives as novel nociceptin/orphanin FQ (N/OFQ) receptor antagonists
    • Sugimoto Y, Shimizu A, Kato T, Satoh A, Ozaki S, Ohta H, Okamoto O. Design, synthesis and biological evaluation of indole derivatives as novel nociceptin/orphanin FQ (N/OFQ) receptor antagonists. Bioorg Med Chem Lett 2006;16:3569-3573.
    • (2006) Bioorg Med Chem Lett , vol.16 , pp. 3569-3573
    • Sugimoto, Y.1    Shimizu, A.2    Kato, T.3    Satoh, A.4    Ozaki, S.5    Ohta, H.6    Okamoto, O.7
  • 187
    • 79959569247 scopus 로고    scopus 로고
    • 4-Aminomethyl-1-aryl-cyclohexylamine compounds. Patent US7173045, Gruenenthal GmbH
    • Sundermann B, Schick H, Hinze C. 4-Aminomethyl-1-aryl-cyclohexylamine compounds. Patent US7173045, Gruenenthal GmbH, 2007.
    • (2007)
    • Sundermann, B.1    Schick, H.2    Hinze, C.3
  • 188
    • 79959568221 scopus 로고    scopus 로고
    • 4-Hydroxymethyl-1-aryl-cyclohexylamine compounds. Patent US7232847, Gruenenthal GmbH
    • Sundermann B, Schick H, Hinze C. 4-Hydroxymethyl-1-aryl-cyclohexylamine compounds. Patent US7232847, Gruenenthal GmbH, 2007.
    • (2007)
    • Sundermann, B.1    Schick, H.2    Hinze, C.3
  • 189
    • 79959559650 scopus 로고    scopus 로고
    • Cyclohexylacetic acid compounds. Patent US20070129347, Gruenenthal GmbH
    • Hinze C, Sundermann B, Schick H, Henkel B. Cyclohexylacetic acid compounds. Patent US20070129347, Gruenenthal GmbH, 2007.
    • (2007)
    • Hinze, C.1    Sundermann, B.2    Schick, H.3    Henkel, B.4
  • 190
    • 79959549481 scopus 로고    scopus 로고
    • Cyclohexylurea compounds. Patent US7348354, Gruenenthal GmbH
    • Hinze C, Schick H. Cyclohexylurea compounds. Patent US7348354, Gruenenthal GmbH, 2008.
    • (2008)
    • Hinze, C.1    Schick, H.2
  • 191
    • 79959568423 scopus 로고    scopus 로고
    • 4-Alkyl-/4-alkenyl/4-alkynyl methyl-/1-aryl-cyclohexylamine compounds. Patent US7507758, Gruenenthal GmbH
    • Sundermann B, Schick H. 4-Alkyl-/4-alkenyl/4-alkynyl methyl-/1-aryl-cyclohexylamine compounds. Patent US7507758, Gruenenthal GmbH, 2009.
    • (2009)
    • Sundermann, B.1    Schick, H.2
  • 192
    • 79959545187 scopus 로고    scopus 로고
    • Substituted 4-aminocyclohexanols. Patent US7211694, Gruenenthal GmbH
    • Sundermann B, Hennies HH, Englberger W, Koegel BY. Substituted 4-aminocyclohexanols. Patent US7211694, Gruenenthal GmbH, 2007.
    • (2007)
    • Sundermann, B.1    Hennies, H.H.2    Englberger, W.3    Koegel, B.Y.4
  • 193
    • 79959535508 scopus 로고    scopus 로고
    • Substituted 2-pyridine-cyclohexane-1,4-diamine derivatives. Patent EP1385825, Gruenenthal GmbH
    • Sundermann B, Maul C, Buschmann H, Heller B. Substituted 2-pyridine-cyclohexane-1, 4-diamine derivatives. Patent EP1385825, Gruenenthal GmbH, 2007.
    • (2007)
    • Sundermann, B.1    Maul, C.2    Buschmann, H.3    Heller, B.4
  • 194
    • 79959565997 scopus 로고    scopus 로고
    • Substituted cyclohexane-1,4-diamine compounds. Patent US7276518, Gruenenthal GmbH
    • Sundermann B, Hennies HH, Englberger W, Koegel BY. Substituted cyclohexane-1, 4-diamine compounds. Patent US7276518, Gruenenthal GmbH, 2007.
    • (2007)
    • Sundermann, B.1    Hennies, H.H.2    Englberger, W.3    Koegel, B.Y.4
  • 195
    • 79959568019 scopus 로고    scopus 로고
    • Cyclohexyl-1,4-diamine compounds. Patent US7439394, Gruenenthal GmbH
    • Sundermann C, Sundermann B. Cyclohexyl-1, 4-diamine compounds. Patent US7439394, Gruenenthal GmbH, 2008.
    • (2008)
    • Sundermann, C.1    Sundermann, B.2
  • 197
    • 84857112845 scopus 로고    scopus 로고
    • Spirocyclic cyclohexane compounds useful to treat substance dependency. Patent US 20080221141, Gruenenthal GmbH
    • Friderichs E, Kögel BY, Linz K. Spirocyclic cyclohexane compounds useful to treat substance dependency. Patent US 20080221141, Gruenenthal GmbH, 2008.
    • (2008)
    • Friderichs, E.1    Kögel, B.Y.2    Linz, K.3
  • 198
    • 84857108778 scopus 로고    scopus 로고
    • Mixed ORL1/mu agonists for the treatment of pain. Patent US 2008/0125475; Gruenenthal GmbH
    • Linz K, Kögel BY, Schröder W, Christoph T, De Vry J, Friderichs E. Mixed ORL1/mu agonists for the treatment of pain. Patent US 2008/0125475; Gruenenthal GmbH, 2008.
    • (2008)
    • Linz, K.1    Kögel, B.Y.2    Schröder, W.3    Christoph, T.4    De Vry, J.5    Friderichs, E.6
  • 200
    • 79959570171 scopus 로고    scopus 로고
    • Phenylpropionamide compounds and the use thereof. Patent WO/2008/053352, Purdue Pharma L.P.
    • Zhou X. Phenylpropionamide compounds and the use thereof. Patent WO/2008/053352, Purdue Pharma L.P., 2008.
    • (2008)
    • Zhou, X.1
  • 201
    • 0037020755 scopus 로고    scopus 로고
    • Synthesis and structure-activity relationships of aminoalkylazetidines as ORL1 receptor ligands
    • Wu WL, Caplen MA, Domalski MS, Zhang H, Fawzi A, Burnett DA. Synthesis and structure-activity relationships of aminoalkylazetidines as ORL1 receptor ligands. Bioorg Med Chem Lett 2002;12:3157-3160.
    • (2002) Bioorg Med Chem Lett , vol.12 , pp. 3157-3160
    • Wu, W.L.1    Caplen, M.A.2    Domalski, M.S.3    Zhang, H.4    Fawzi, A.5    Burnett, D.A.6
  • 203
    • 79959539332 scopus 로고    scopus 로고
    • Aryl-substituted nitrogen-containing heterocyclic compound. Patent EP1935881, Banyu Pharmaceutical Co. Ltd.
    • Okamoto O, Kobayashi K, Ito H, Tsujita T, Ozaki S, Ohta H. Aryl-substituted nitrogen-containing heterocyclic compound. Patent EP1935881, Banyu Pharmaceutical Co. Ltd., 2008.
    • (2008)
    • Okamoto, O.1    Kobayashi, K.2    Ito, H.3    Tsujita, T.4    Ozaki, S.5    Ohta, H.6


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