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Volumn 6, Issue 8, 2003, Pages 758-772

Antagonists at the neurokinin receptors - Recent patent literature

Author keywords

Combined neurokinen receptor antagonists; NK1 receptor; NK2 receptor; NK3 receptor

Indexed keywords

3 (2 METHOXYBENZYLAMINO) 2 PHENYLPIPERIDINE; 3 [1 [2 [4 BENZOYL 2 (3,4 DIFLUOROPHENYL) 2 MORPHOLINYL]ETHYL] 4 PHENYL 4 PIPERIDINYL] 1,1 DIMETHYLUREA; 5 AMINOVALERYLSUBSTANCE P [7-11][9 PROLINE 10 (N METHYLLEUCINE)]; 6 MORPHOLINYL 4 TOLYLPYRIDINE DERIVATIVE; ANTIEMETIC AGENT; ANTINEOPLASTIC AGENT; APREPITANT; CASOPITANT; CISPLATIN; DIAZASPIROUNDECANONE DERIVATIVE; EZLOPITANT; NEPADUTANT; NEUROKININ 1 RECEPTOR ANTAGONIST; NEUROKININ 2 RECEPTOR ANTAGONIST; NEUROKININ 3 RECEPTOR ANTAGONIST; OSANETANT; PIPERIDINE DERIVATIVE; PYRIMIDINE DERIVATIVE; R 673; SAREDUTANT; SB 235375; SB 400238; SB 414240; SPIRO COMPOUND; SUBSTANCE P; SUBSTANCE P DERIVATIVE; TACHYKININ RECEPTOR ANTAGONIST; TAK 637; TALNETANT; UK 224671; UK 290795; UNCLASSIFIED DRUG; UNINDEXED DRUG; VESTIPITANT; VOFOPITANT; ZD 2249; ZD 4974; ZD 6021;

EID: 0043195904     PISSN: 13697056     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (33)

References (95)
  • 1
    • 0035207423 scopus 로고    scopus 로고
    • 1 receptor antagonists for the control of chemotherapy-induced nausea and vomiting
    • 1 receptor antagonists for the control of chemotherapy-induced nausea and vomiting. Exp Opin Ther Patents (2001) 11(12):1837-1847.
    • (2001) Exp Opin Ther Patents , vol.11 , Issue.12 , pp. 1837-1847
    • Gale, J.D.1    O'Neill, B.T.2    Humphrey, J.M.3
  • 4
    • 0036122109 scopus 로고    scopus 로고
    • Substance P and affective disorders: New treatment opportunities by neurokinin 1 receptor antagonists?
    • Lieb K, Treffurth Y, Berger M, Fiebich BL: Substance P and affective disorders: New treatment opportunities by neurokinin 1 receptor antagonists? Neuropsychobiology (2002) 45(Suppl 1):2-6.
    • (2002) Neuropsychobiology , vol.45 , Issue.SUPPL. 1 , pp. 2-6
    • Lieb, K.1    Treffurth, Y.2    Berger, M.3    Fiebich, B.L.4
  • 5
    • 0035042259 scopus 로고    scopus 로고
    • Neurokinin(1) receptor antagonists as potential antidepressants
    • Stout SC, Owens MJ, Nemeroff CB: Neurokinin(1) receptor antagonists as potential antidepressants. Annu Rev Pharmacol Toxicol (2001) 41:877-906.
    • (2001) Annu Rev Pharmacol Toxicol , vol.41 , pp. 877-906
    • Stout, S.C.1    Owens, M.J.2    Nemeroff, C.B.3
  • 7
    • 0042520295 scopus 로고    scopus 로고
    • December 2001 - Investor presentation
    • November 21
    • Roche Holding AG: December 2001 - Investor presentation. Company Presentation (2001) November 21.
    • (2001) Company Presentation
  • 8
    • 15144354434 scopus 로고    scopus 로고
    • Structural optimisation affording 2-(R)-(1-(R)-3,5-Bis(trifluoromethyl)phenylethoxy)-3-(S)-(4-fluoro)phenyl-4-(3-o xo-1,2,4-triazol-5-yl)methylmorpholine, a potent orally active, long-acting morpholine acetal human NK-1 receptor antagonist
    • note
    • Hale JH, Mills SG, MacCoss M, Finke PE, Cascieri MA, Sadowski S, Ber E, Chicchi GG, Kurtz M, Metzger J, Eiermann G et al. Structural optimisation affording 2-(R)-(1-(R)-3,5-Bis(trifluoromethyl)phenylethoxy)-3-(S)-(4-fluoro)phenyl-4-(3-o xo-1,2,4-triazol-5-yl)methylmorpholine, a potent orally active, long-acting morpholine acetal human NK-1 receptor antagonist. J Med Chem (1998) 41(23):4607-4614. This paper discloses aprepitant and its outstanding pharmacological profile that allowed Merck to enter it into clinical developmental for emesis and depression.
    • (1998) J Med Chem , vol.41 , Issue.23 , pp. 4607-4614
    • Hale, J.H.1    Mills, S.G.2    MacCoss, M.3    Finke, P.E.4    Cascieri, M.A.5    Sadowski, S.6    Ber, E.7    Chicchi, G.G.8    Kurtz, M.9    Metzger, J.10    Eiermann, G.11
  • 9
    • 0043021335 scopus 로고    scopus 로고
    • FDA grants Priority Review for EMEND, Merck's investigational medicine for prevention of chemotherapy-induced nausea and vomiting
    • December 09
    • Merck & Co Inc: FDA grants Priority Review for EMEND, Merck's investigational medicine for prevention of chemotherapy-induced nausea and vomiting. Press Release (2002) December 09.
    • (2002) Press Release
  • 10
    • 0036008323 scopus 로고    scopus 로고
    • 1 receptor antagonists on the viscerosensory response caused by colorectal distention in rabbits
    • 1 receptor antagonists on the viscerosensory response caused by colorectal distention in rabbits. J Pharmacol Exp Ther (2002) 300(3):925-931.
    • (2002) J Pharmacol Exp Ther , vol.300 , Issue.3 , pp. 925-931
    • Okano, S.1    Ikeura, Y.2    Inatomi, N.3
  • 11
    • 0042019432 scopus 로고    scopus 로고
    • Effects of TAK-637, a neurokinin-1 (NK) receptor antagonist, on stress-induced defecation in mongolian gerbils
    • Okano S, Nagaya H, Inatomi N: Effects of TAK-637, a neurokinin-1 (NK) receptor antagonist, on stress-induced defecation in mongolian gerbils. Jpn J Pharmacol (2001) 85:220.
    • (2001) Jpn J Pharmacol , vol.85 , pp. 220
    • Okano, S.1    Nagaya, H.2    Inatomi, N.3
  • 12
    • 0034057760 scopus 로고    scopus 로고
    • Pharmacological blockade or genetic deletion of substance P (NK-1) receptors attenuates neonatal vocalisation in guinea-pigs and mice
    • Rupniak NMJ, Carlson EC, Harrison T, Oates B, Seward E, Owen S, De Felipe C, Hunt S, Wheeldon A: Pharmacological blockade or genetic deletion of substance P (NK-1) receptors attenuates neonatal vocalisation in guinea-pigs and mice. Neuropharmacology (2000) 39(8):1413-1421.
    • (2000) Neuropharmacology , vol.39 , Issue.8 , pp. 1413-1421
    • Rupniak, N.M.J.1    Carlson, E.C.2    Harrison, T.3    Oates, B.4    Seward, E.5    Owen, S.6    De, F.C.7    Hunt, S.8    Wheeldon, A.9
  • 16
    • 0036089360 scopus 로고    scopus 로고
    • Irritable bowel syndrome neuropharmacology. A review of approved and investigational compounds
    • Callahan MJ: Irritable bowel syndrome neuropharmacology. A review of approved and investigational compounds. J Clin Gastroenterol (2002) 35(Suppl 1):58-67.
    • (2002) J Clin Gastroenterol , vol.35 , Issue.SUPPL. 1 , pp. 58-67
    • Callahan, M.J.1
  • 17
    • 24844445993 scopus 로고    scopus 로고
    • Research & development
    • Research & development: The Menarini Group, Pomezia, Italy. http://www.menarini.com/english/ricerca_sviluppo/nepadutant.htm
  • 19
    • 0042520293 scopus 로고    scopus 로고
    • Financial Analysts Meeting: Information meeting - 18 & 19 February, 2003
    • February 18-19
    • Sanofi-Synthélabo: Financial Analysts Meeting: Information meeting - 18 & 19 February, 2003. Company Presentation (2003) February 18-19.
    • (2003) Company Presentation
  • 20
    • 0041518450 scopus 로고    scopus 로고
    • Balancing potency and oral bioavailability. The design and profile of neurokinin-2-antagonists for the treatment of urinary urge incontinence
    • MEDI 137
    • Middleton D: Balancing potency and oral bioavailability. The design and profile of neurokinin-2-antagonists for the treatment of urinary urge incontinence. 223rd ACS Meeting, Orlando, FL, USA (2002):MEDI 137.
    • (2002) 223rd ACS Meeting, Orlando, FL, USA
    • Middleton, D.1
  • 21
    • 0033730609 scopus 로고    scopus 로고
    • The role of P-glycoprotein in determining the oral absorption and clearance of the NK-2 antagonist, UK-224671
    • Beaumont K, Harper A, Smith DA, Bennett J: The role of P-glycoprotein in determining the oral absorption and clearance of the NK-2 antagonist, UK-224671. Eur J Pharm Sci (2002) 12(1):41-50.
    • (2002) Eur J Pharm Sci , vol.12 , Issue.1 , pp. 41-50
    • Beaumont, K.1    Harper, A.2    Smith, D.A.3    Bennett, J.4
  • 22
    • 0042520294 scopus 로고    scopus 로고
    • Turning peptidic G-protein coupled receptor ligands into drugs
    • 30 June - 01 July
    • Beaumont K: Turning peptidic G-protein coupled receptor ligands into drugs. SMi Conf - G-Protein Coupled Receptors (2003) 30 30 June - 01 July.
    • (2003) SMi Conf - G-Protein Coupled Receptors
    • Beaumont, K.1
  • 28
    • 0033602522 scopus 로고    scopus 로고
    • Discovery of a novel class of selective non-peptide antagonists for the human neurokinin-3 receptor. 2. Identification of (S)-N-(1-phenylpropyl)-3-hydroxy-2-phenylquinoline-4-carboxamide (SB 223412)
    • Giardina GAM, Raveglia LF, Grugni M, Sarau HM, Farina C, Medhurst AD, Graziani D, Schmidt DB, Rigolio R, Luttmann M, Cavagnera S et al. Discovery of a novel class of selective non-peptide antagonists for the human neurokinin-3 receptor. 2. Identification of (S)-N-(1-phenylpropyl)-3-hydroxy-2-phenylquinoline-4-carboxamide (SB 223412). J Med Chem (1999) 42(6):1053-1065.
    • (1999) J Med Chem , vol.42 , Issue.6 , pp. 1053-1065
    • Giardina, G.A.M.1    Raveglia, L.F.2    Grugni, M.3    Sarau, H.M.4    Farina, C.5    Medhurst, A.D.6    Graziani, D.7    Schmidt, D.B.8    Rigolio, R.9    Luttmann, M.10    Cavagnera, S.11
  • 30
    • 0042019433 scopus 로고    scopus 로고
    • Product development pipeline
    • February 12
    • GlaxoSmithKline plc: Product development pipeline. Company Publication (2003) February 12.
    • (2003) Company Publication
  • 32
    • 18244395370 scopus 로고    scopus 로고
    • Nonpeptide tachykinin receptor antagonists. III. SB 235375, a low central nervous system-penetrant, potent and selective neurokinin-3 receptor antagonist, inhibits citric-acid-induced cough and airways hyperreactivity in guinea pigs
    • Hay DWP, Giardina GAM, Griswold DE, Underwood D, Kotzer C, Bush B, Potts W, Sandhu P, Lundberg D, Foley JJ, Schmidt DB et al: Nonpeptide tachykinin receptor antagonists. III. SB 235375, a low central nervous system-penetrant, potent and selective neurokinin-3 receptor antagonist, inhibits citric-acid-induced cough and airways hyperreactivity in guinea pigs. J Pharmacol Exp Ther (2002) 300(1):314-323.
    • (2002) J Pharmacol Exp Ther , vol.300 , Issue.1 , pp. 314-323
    • Hay, D.W.P.1    Giardina, G.A.M.2    Griswold, D.E.3    Underwood, D.4    Kotzer, C.5    Bush, B.6    Potts, W.7    Sandhu, P.8    Lundberg, D.9    Foley, J.J.10    Schmidt, D.B.11
  • 33
    • 0042019431 scopus 로고    scopus 로고
    • Methods of treatment comprising administration of substance P
    • WO-00243748
    • Milkhaus Laboratory Inc (Lieberman AD, McMichel J): Methods of treatment comprising administration of substance P. WO-00243748 (2002).
    • (2002)
    • Lieberman, A.D.1    McMichel, J.2
  • 34
    • 53749092696 scopus 로고    scopus 로고
    • Substance P analogs for the treatment of cancer
    • WO-00210194
    • Dabur Research Foundation (Burman AC, Prasad S, Mukherhee R, Jaggi M, Singh AT): Substance P analogs for the treatment of cancer. WO-00210194 (2002).
    • (2002)
    • Burman, A.C.1    Prasad, S.2    Mukherhee, R.3    Jaggi, M.4    Singh, A.T.5
  • 35
    • 4243376112 scopus 로고    scopus 로고
    • Pyrimidine derivatives
    • WO-00242280
    • F Hoffman-La Roche AG (Stadler H): Pyrimidine derivatives. WO-00242280 (2002).
    • (2002)
    • Stadler, H.1
  • 36
    • 0042520288 scopus 로고    scopus 로고
    • 4-Phenyl-pyridine derivatives as neurokinin-1 receptor antagonists
    • WO-00208232
    • F Hoffman-La Roche AG (Hoffmann, T, Schnider P, Stadler H): 4-Phenyl-pyridine derivatives as neurokinin-1 receptor antagonists. WO-00208232 (2002).
    • (2002)
    • Hoffmann, T.1    Schnider, P.2    Stadler, H.3
  • 37
    • 0042520288 scopus 로고    scopus 로고
    • 4-Phenyl-pyridine derivatives as neurokinin-1 receptor antagonists
    • WO-00216324
    • F Hoffman-La Roche AG (Godel T, Hoffmann T, Schnider P, Stadler H): 4-Phenyl-pyridine derivatives as neurokinin-1 receptor antagonists. WO-00216324 (2002).
    • (2002)
    • Godel, T.1    Hoffmann, T.2    Schnider, P.3    Stadler, H.4
  • 38
    • 4243724718 scopus 로고    scopus 로고
    • Process for the manufacture of phenylacetic acid derivatives
    • WO-02079134
    • F Hoffman-La Roche AG (Hoffmann-Emery F, Scalone M, Spurr P): Process for the manufacture of phenylacetic acid derivatives. WO-02079134 (2002).
    • (2002)
    • Hoffmann-Emery, F.1    Scalone, M.2    Spurr, P.3
  • 39
  • 40
    • 0043021334 scopus 로고    scopus 로고
    • Use of NK-1 receptor antagonists against benign prostatic hyperplasia
    • WO-02085458
    • F Hoffman-La Roche AG (Buser S, Ford APDW, Hoffmann T, Lenz B, Sleight AJ, Vankan P): Use of NK-1 receptor antagonists against benign prostatic hyperplasia. WO-02085458 (2002).
    • (2002)
    • Buser, S.1    Ford, A.P.D.W.2    Hoffmann, T.3    Lenz, B.4    Sleight, A.J.5    Vankan, P.6
  • 41
    • 24844446936 scopus 로고    scopus 로고
    • Self emulsifying lipid matrix (selm)
    • WO-00247663
    • F Hoffman-La Roche AG (Kuentz M, Roethlisberger D): Self emulsifying lipid matrix (selm). WO-00247663 (2002).
    • (2002)
    • Kuentz, M.1    Roethlisberger, D.2
  • 42
    • 24844436367 scopus 로고    scopus 로고
    • Piperidine derivatives as neurokinin 1 antagonists
    • WO-02062784
    • F Hoffman-La Roche AG (Kolczewski S, Roever S, Schnider P): Piperidine derivatives as neurokinin 1 antagonists. WO-02062784 (2002).
    • (2002)
    • Kolczewski, S.1    Roever, S.2    Schnider, P.3
  • 43
    • 0042520286 scopus 로고    scopus 로고
    • 1-Oxa-3,9-diaza-spiro[5.5]-undecan-2-ones derivatives and their use as antagonist of the neurokinin receptor
    • WO-02092604
    • F Hoffman-La Roche AG (Cai HY, Dillon MP, Galley G, Goergler A, Kolcewsky S, Muszynski-Barsy DM): 1-Oxa-3,9-diaza-spiro[5.5]-undecan-2-ones derivatives and their use as antagonist of the neurokinin receptor. WO-02092604 (2002).
    • (2002)
    • Cai, Y.1    Dillon, M.P.2    Galley, G.3    Goergler, A.4    Kolcewsky, S.5    Muszynski-Barsy, D.M.6
  • 45
    • 4243369884 scopus 로고    scopus 로고
    • Azabicyclic spiroether derivatives and their use as therapeutic agents
    • US-06479486
    • Merck Sharp & Dohme Ltd (Huscroft IT, Kulagowski JJ, Raubo PA): Azabicyclic spiroether derivatives and their use as therapeutic agents. US-06479486 (2002).
    • (2002)
    • Huscroft, I.T.1    Kulagowski, J.J.2    Raubo, P.A.3
  • 47
    • 24844479602 scopus 로고    scopus 로고
    • Tetrahydropyran derivatives as neurokinin receptor agonists
    • WO-02057250
    • Merck Sharp & Dohme Ltd (Castro Piniero JL, Rabuo PA, Swain CJ): Tetrahydropyran derivatives as neurokinin receptor agonists. WO-02057250 (2002).
    • (2002)
    • Castro Piniero, J.L.1    Rabuo, P.A.2    Swain, C.J.3
  • 48
    • 0043021331 scopus 로고    scopus 로고
    • Tetrahydrofuran derivatives and their use as NK-1 antagonists
    • WO-00224673
    • Merck Sharp & Dohme Ltd (Owen SN, Swain CJ, Williams BJ): Tetrahydrofuran derivatives and their use as NK-1 antagonists. WO-00224673 (2002).
    • (2002)
    • Owen, S.N.1    Swain, C.J.2    Williams, B.J.3
  • 49
    • 4244120115 scopus 로고    scopus 로고
    • Zwitterionic tachykinin receptor antagonists
    • WO-00224629
    • Merck & Co Inc (Finke PE, Meurer LC, Mills SG, Maccoss M, Qi H): Zwitterionic tachykinin receptor antagonists. WO-00224629 (2002).
    • (2002)
    • Finke, P.E.1    Meurer, L.C.2    Mills, S.G.3    Maccoss, M.4    Qi, H.5
  • 50
    • 4243486430 scopus 로고    scopus 로고
    • Mammalian metabolites of a tachykinin receptor antagonist
    • WO-00234699 (2002)
    • Merck & Co Inc (Huskey SW, Chiu SL): Mammalian metabolites of a tachykinin receptor antagonist. WO-00234699 (2002).
    • (2002)
    • Huskey, S.W.1    Chiu, S.L.2
  • 52
    • 4243812756 scopus 로고    scopus 로고
    • Preventives/remedies for emotional disorders
    • WO-00226260
    • Takeda Chemical Industries Ltd (Doi T, Ban T) Preventives/remedies for emotional disorders. WO-00226260 (2002).
    • (2002)
    • Doi, T.1    Ban, T.2
  • 53
    • 24844469916 scopus 로고    scopus 로고
    • Tricyclic heterocyclic compound, process for producing the same, and use
    • WO-02074771
    • Takeda Chemical Industries Ltd (Ikeura Y, Hashimoto T, Tarui N, Kamo I, Shirai J:) Tricyclic heterocyclic compound, process for producing the same, and use. WO-02074771 (2002).
    • (2002)
    • Ikeura, Y.1    Hashimoto, T.2    Tarui, N.3    Kamo, I.4    Shirai, J.5
  • 55
    • 0042019373 scopus 로고    scopus 로고
    • [1,4]-Diazepane-1-carboxylic acid derivatives process for their preparation and their use as tachykinin antagonists
    • WO-02081457
    • Glaxo Wellcome plc (Alvaro G:) [1,4]-Diazepane-1-carboxylic acid derivatives process for their preparation and their use as tachykinin antagonists. WO-02081457 (2002).
    • (2002)
    • Alvaro, G.1
  • 56
    • 4243419694 scopus 로고    scopus 로고
    • Piperazine derivatives as tachykinin antagonists
    • WO-02081461
    • Glaxo Wellcome plc (Pentassuglia G:) Piperazine derivatives as tachykinin antagonists. WO-02081461 (2002).
    • (2002)
    • Pentassuglia, G.1
  • 58
    • 0042019372 scopus 로고    scopus 로고
    • N-Triazolylmethyl-piperazine derivatives as neurokinin receptor-antagonists
    • EP-01176144
    • Solvay Pharmaceuticals GmbH (Jasserand D, Schon U, Sann H, Bruckner R, Eeckhout C:) N-Triazolylmethyl-piperazine derivatives as neurokinin receptor-antagonists. EP-01176144 (2002).
    • (2002)
    • Jasserand, D.1    Schon, U.2    Sann, H.3    Bruckner, R.4    Eeckhout, C.5
  • 59
    • 4243376111 scopus 로고    scopus 로고
    • Novel neurokinin antagonists, method for the production thereof and pharmaceutical compositions containing said compounds
    • WO-00232865
    • Boehringer Ingelheim Pharma KG (Dollinger H, Esser F, Jung B, Schromm K, Speck G:) Novel neurokinin antagonists, method for the production thereof and pharmaceutical compositions containing said compounds. WO-00232865 (2002).
    • (2002)
    • Dollinger, H.1    Esser, F.2    Jung, B.3    Schromm, K.4    Speck, G.5
  • 60
    • 0041518380 scopus 로고    scopus 로고
    • (4-Acylaminopiperidin-1-yl)acetamides as neurokinin antagonists
    • WO-00232866
    • Boehringer Ingelheim Pharma KG (Dollinger H, Esser F, Jung B, Schnorrenberg G, Schromm K, Speck G:) (4-Acylaminopiperidin-1-yl)acetamides as neurokinin antagonists. WO-00232866 (2002).
    • (2002)
    • Dollinger, H.1    Esser, F.2    Jung, B.3    Schnorrenberg, G.4    Schromm, K.5    Speck, G.6
  • 61
    • 24844453412 scopus 로고    scopus 로고
    • Novel aryl glycinamide derivatives, method of producing said derivatives and pharmaceutical compositions containing these compounds
    • WO-09732865
    • Boehringer Ingelheim Pharma KG (Esser F, Schnorrenberg G, Schromm K, Dollinger H, Jung B, Speck G:) Novel aryl glycinamide derivatives, method of producing said derivatives and pharmaceutical compositions containing these compounds. WO-09732865 (1997).
    • (1997)
    • Esser, F.1    Schnorrenberg, G.2    Schromm, K.3    Dollinger, H.4    Jung, B.5    Speck, G.6
  • 62
    • 4243529870 scopus 로고    scopus 로고
    • Aryl glycinamide derivatives, method of producing these substances and pharmaceutical compositions containing such compounds
    • WO-09632386
    • Boehringer Ingelheim Pharma KG (Schnorrenberg G, Dollinger H, Esser F, Briem H, Jung B, Speck G): Aryl glycinamide derivatives, method of producing these substances and pharmaceutical compositions containing such compounds. WO-09632386 (1996).
    • (1996)
    • Schnorrenberg, G.1    Dollinger, H.2    Esser, F.3    Briem, H.4    Jung, B.5    Speck, G.6
  • 63
    • 0041518374 scopus 로고    scopus 로고
    • Use of fluoroalkoxybenzylamino derivatives of nitrogen containing heterocycles as substance P receptor antagonists
    • EP-01172106
    • Pfizer Product Inc (Neill BT, Saltarelli MD:) Use of fluoroalkoxybenzylamino derivatives of nitrogen containing heterocycles as substance P receptor antagonists. EP-01172106 (2002).
    • (2002)
    • Neill, B.T.1    Saltarelli, M.D.2
  • 64
    • 24844473806 scopus 로고    scopus 로고
    • Basic compounds containing tertiary amides with activity on tachykinin receptors, and pharmaceutical compositions containing them
    • WO-00220437
    • Menarini Ricerche SpA (Guidi A. Pasqui F, Altamura M, Maggi CA:) Basic compounds containing tertiary amides with activity on tachykinin receptors, and pharmaceutical compositions containing them. WO-00220437 (2002).
    • (2002)
    • Guidi, A.1    Pasqui, F.2    Altamura, M.3    Maggi, C.A.4
  • 65
    • 4243946108 scopus 로고    scopus 로고
    • Novel naphthyridine derivatives or their pharmacologically acceptable salts
    • JP-14088081
    • Nippon Kayaku Co Ltd (Adzuma S, Yamamoto T, Amayama Y, Ishida A:) Novel naphthyridine derivatives or their pharmacologically acceptable salts. JP-14088081 (2002).
    • (2002)
    • Adzuma, S.1    Yamamoto, T.2    Amayama, Y.3    Ishida, A.4
  • 66
    • 4243724078 scopus 로고    scopus 로고
    • Process for producing novel naphthyridine derivatives
    • US-06433174
    • Nippon Kayaku Co Ltd (Satoh Y, Tsuda M, Nagai M, Yamazaki H:) Process for producing novel naphthyridine derivatives. US-06433174 (2002).
    • (2002)
    • Satoh, Y.1    Tsuda, M.2    Nagai, M.3    Yamazaki, H.4
  • 67
    • 24844434639 scopus 로고    scopus 로고
    • Cyclized benzamide neurokinin antagonists for use in therapy
    • WO-00226724
    • AstraZeneca AB (Bernstein P:) Cyclized benzamide neurokinin antagonists for use in therapy. WO-00226724 (2002).
    • (2002)
    • Bernstein, P.1
  • 68
    • 0042520226 scopus 로고    scopus 로고
    • Novel N-(2-phenyl-3-aminopropyl)naphthamides
    • WO-00212168
    • AstraZeneca AB (Bernstein P:) Novel N-(2-phenyl-3-aminopropyl)naphthamides. WO-00212168 (2002).
    • (2002)
    • Bernstein, P.1
  • 69
    • 0042520234 scopus 로고    scopus 로고
    • Compounds
    • WO-02051807
    • AstraZeneca AB (Shenvi AB:) Compounds. WO-02051807 (2002).
    • (2002)
    • Shenvi, A.B.1
  • 70
    • 24844480124 scopus 로고    scopus 로고
    • Novel piperidine carboxamide derivatives, method for preparing same and pharmaceutical compositions containing same
    • WO-02094821
    • Sanofi-Synthélabo (Emonds-Alt X, Proietto V:) Novel piperidine carboxamide derivatives, method for preparing same and pharmaceutical compositions containing same. WO-02094821 (2002).
    • (2002)
    • Emonds-Alt, X.1    Proietto, V.2
  • 72
    • 0043021274 scopus 로고    scopus 로고
    • Quinolone-4-carboxamide derivatives as NK-3 and NK-2 receptor antagonists
    • WO-00238548
    • GlaxoSmithKline SpA (Farina C, Giardina GAM, Grugni M, Nadler GMMG:) Quinolone-4-carboxamide derivatives as NK-3 and NK-2 receptor antagonists. WO-00238548 (2002).
    • (2002)
    • Farina, C.1    Giardina, G.A.M.2    Grugni, M.3    Nadler, G.M.M.G.4
  • 76
    • 0041517990 scopus 로고    scopus 로고
    • 3-Substituted quinoline-4-carboxamide derivatives as NK-3 and NK-2 receptor antagonists
    • WO-02083664
    • GlaxoSmithKline SpA (Farina C, Gagliardi S, Giardina GAM, Martinelli M:) 3-Substituted quinoline-4-carboxamide derivatives as NK-3 and NK-2 receptor antagonists. WO-02083664 (2002).
    • (2002)
    • Farina, C.1    Gagliardi, S.2    Giardina, G.A.M.3    Martinelli, M.4
  • 77
    • 0043021274 scopus 로고    scopus 로고
    • Quinoline-4-carboxamide derivatives as NK-3 and NK-2 receptor antagonists
    • WO-02083663
    • GlaxoSmithKline SpA (Farina C, Gagliardi S, Giardina GAM, Martinelli M:) Quinoline-4-carboxamide derivatives as NK-3 and NK-2 receptor antagonists. WO-02083663 (2002).
    • (2002)
    • Farina, C.1    Gagliardi, S.2    Giardina, G.A.M.3    Martinelli, M.4
  • 79
    • 0041518377 scopus 로고    scopus 로고
    • Quinoline 4-carboxamide derivatives as NK-2 and NK-3 receptor antagonists
    • WO-00031037
    • SmithKline Beecham SpA (Farina C, Giardina GAM, Grugni M:) Quinoline 4-carboxamide derivatives as NK-2 and NK-3 receptor antagonists. WO-00031037 (2000).
    • (2000)
    • Farina, C.1    Giardina, G.A.M.2    Grugni, M.3
  • 80
    • 0042019369 scopus 로고    scopus 로고
    • Quinoline derivatives as NK-2 and NK-3 receptor ligands
    • WO-0031038
    • SmithKline Beecham SpA/SmithKline Beecham Laboratoires Pharmaceutiques (Farina C, Giardina GAM, Grugni M, Nadler GMMG:) Quinoline derivatives as NK-2 and NK-3 receptor ligands. WO-0031038 (2000).
    • (2000)
    • Farina, C.1    Giardina, G.A.M.2    Grugni, M.3    Nadler, G.M.M.G.4
  • 82
    • 0041518378 scopus 로고    scopus 로고
    • 1-(2-Methoxybenzyl)-3-benzhydrylpiperazines as tachykinin antagonists
    • WO-02055518
    • Fujisawa Pharmaceutical Co Ltd (Take K, Kasahara C, Shigenaga S, Azami H, Eikyu Y, Nakai K, Morita M:) 1-(2-Methoxybenzyl)-3-benzhydrylpiperazines as tachykinin antagonists. WO-02055518 (2002).
    • (2002)
    • Take, K.1    Kasahara, C.2    Shigenaga, S.3    Azami, H.4    Eikyu, Y.5    Nakai, K.6    Morita, M.7
  • 83
    • 4243879053 scopus 로고    scopus 로고
    • Novel amidoalkyl-piperidine and amidoalkyl-piperazine derivatives useful for the treatment of nervous system disorders
    • WO-00240466
    • Ortho-McNeil Pharmaceutical Inc (Kordik CP, Reitz AB, Coats SJ, Luo C, Pan K, Parker MH:) Novel amidoalkyl-piperidine and amidoalkyl-piperazine derivatives useful for the treatment of nervous system disorders. WO-00240466 (2002).
    • (2002)
    • Kordik, C.P.1    Reitz, A.B.2    Coats, S.J.3    Luo, C.4    Pan, K.5    Parker, M.H.6
  • 84
    • 24844453948 scopus 로고    scopus 로고
    • Novel use
    • WO-00240023
    • SmithKline Beecham Corporation (Dillon SB, Tal-Singer R:) Novel use. WO-00240023 (2002).
    • (2002)
    • Dillon, S.B.1    Tal-Singer, R.2
  • 86
    • 4243247681 scopus 로고    scopus 로고
    • Novel pharmaceutical use of quinoline derivatives
    • WO-00213825
    • SmithKline Beecham plc (Machin P:) Novel pharmaceutical use of quinoline derivatives. WO-00213825 (2002).
    • (2002)
    • Machin, P.1
  • 87
    • 24844442578 scopus 로고    scopus 로고
    • Method for treating symptoms of hormonal variation, including hot flashes, using tachykinin receptor antagonist
    • WO-00195904
    • University of Rochester (Guttuso TJ:) Method for treating symptoms of hormonal variation, including hot flashes, using tachykinin receptor antagonist. WO-00195904 (2001).
    • (2001)
    • Guttuso, T.J.1
  • 89
    • 24844462315 scopus 로고    scopus 로고
    • Anti-androgens and methods for treating disease
    • WO-00043008
    • SmithKline Beecham Corporation (Murphy DJ, Wier PJ, Giardina GAM:) Anti-androgens and methods for treating disease. WO-00043008 (2000).
    • (2000)
    • Murphy, D.J.1    Wier, P.J.2    Giardina, G.A.M.3
  • 90
    • 84880169182 scopus 로고    scopus 로고
    • Novel solid dispersion compositions
    • WO-00195939
    • SmithKline Beecham Corporation (Koretke TW, Bhatt KH:) Novel solid dispersion compositions. WO-00195939 (2001).
    • (2001)
    • Koretke, T.W.1    Bhatt, K.H.2
  • 91
    • 24844460512 scopus 로고    scopus 로고
    • Combination drugs
    • WO-02051440
    • Takeda Chemical Industries Ltd (Doi T, Hashimoto T, Kamo I:) Combination drugs. WO-02051440 (2002).
    • (2002)
    • Doi, T.1    Hashimoto, T.2    Kamo, I.3
  • 93
    • 0042520229 scopus 로고    scopus 로고
    • Combination for treating depression and anxiety containing an NK-3 receptor antagonist and a CNS penetrant NK-1 receptor antagonist
    • EP-01192952
    • Pfizer Products Inc (Lowe JA, McLean S, Sobolov-Janes SB:) Combination for treating depression and anxiety containing an NK-3 receptor antagonist and a CNS penetrant NK-1 receptor antagonist. EP-01192952 (2002).
    • (2002)
    • Lowe, J.A.1    McLean, S.2    Sobolov-Janes, S.B.3
  • 94
    • 0043021273 scopus 로고    scopus 로고
    • 1 receptor antagonist and a CNS penetrant NK-1 receptor antagonist
    • EP-01186318
    • 1 receptor antagonist and a CNS penetrant NK-1 receptor antagonist. EP-01186318 (2002).
    • (2002)
    • Schimdt, C.J.1    Sobolov-Jaynes, S.B.2
  • 95
    • 0041518376 scopus 로고    scopus 로고
    • Oligonucleotides and other modulators of the NK-1 receptor pathway and therapeutic uses thereof
    • WO-00213799
    • McGill University (Henry JL, Cahill CM, Yashpal K:) Oligonucleotides and other modulators of the NK-1 receptor pathway and therapeutic uses thereof. WO-00213799 (2002).
    • (2002)
    • Henry, J.L.1    Cahill, C.M.2    Yashpal, K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.