메뉴 건너뛰기




Volumn 23, Issue 8, 2013, Pages 1057-1068

Corticotropin-releasing factor 1 receptor antagonists: A patent review

Author keywords

Adrenocorticotropic hormone; Corticotropin releasing factor; CRF1 antagonist; Stress

Indexed keywords

2 THIENYL; 3 (6 DIMETHYLAMINO 4 METHYL 3 PYRIDINYL) 7 DIPROPYLAMINO 2,5 DIMETHYLPYRAZOLO[1,5 A]PYRIMIDINE; 5 THIAZOLYL; 5,5 BICYCLIC IMIDAZO[4,5 C]PYRAZOLE; 5,5 BICYCLIC PYRAZOLO[3,2 B ][1,3]OXAZOLE; CORTICOTROPIN RELEASING FACTOR ANTAGONIST; CORTICOTROPIN RELEASING FACTOR RECEPTOR 1; CP 316 311; CP 3160311; HORMONE RECEPTOR BLOCKING AGENT; IMIDAZO[1,2 B]PYRIDAZINE; IMIDAZOPYRIDINE DERIVATIVE; NBI 34041; PEXACERFONT; PYRAZOLE DERIVATIVE; PYRAZOLO[3,2 B][1,3]THIAZOLE; PYRAZOLONE; PYRAZOLOPYRIMIDINE DERIVATIVE; SR 125543; THIAZOLE DERIVATIVE; UNCLASSIFIED DRUG; VERUCERFONT;

EID: 84880684989     PISSN: 13543776     EISSN: 17447674     Source Type: Journal    
DOI: 10.1517/13543776.2013.795545     Document Type: Review
Times cited : (16)

References (77)
  • 1
    • 0019782980 scopus 로고
    • Characterization of a 41-residue ovine hypothalamic peptide that stimulates secretion of corticotropin and beta-endorphin
    • Vale WW, Spiess J, Rivier C, Rivier J Characterization of a 41-residue ovine hypothalamic peptide that stimulates secretion of corticotropin and beta-endorphin Science 1981;213:1394-7
    • (1981) Science , vol.213 , pp. 1394-1397
    • Vale, W.W.1    Spiess, J.2    Rivier, C.3    Rivier, J.4
  • 2
    • 0027489208 scopus 로고
    • Expression cloning of a human corticotropin-releasing factor receptor
    • Chen R, Lewis KA, Perrin MH, Vale WW Expression cloning of a human corticotropin-releasing factor receptor Proc Natl Acad Sci USA 1993;90:8967-71
    • (1993) Proc Natl Acad Sci USA , vol.90 , pp. 8967-8971
    • Chen, R.1    Lewis, K.A.2    Perrin, M.H.3    Vale, W.W.4
  • 3
    • 0028800601 scopus 로고
    • Cloning and characterization of a functionally distinct corticotropin-releasing factor receptor subtype from rat brain
    • Lovenberg TW, Liaw CW, Grigoriadis DE, et al Cloning and characterization of a functionally distinct corticotropin-releasing factor receptor subtype from rat brain Proc Natl Acad Sci USA 1995;92:836-40
    • (1995) Proc Natl Acad Sci USA , vol.92 , pp. 836-840
    • Lovenberg, T.W.1    Liaw, C.W.2    Grigoriadis, D.E.3
  • 4
    • 0029981998 scopus 로고    scopus 로고
    • Cloning and characterization of human urocortin
    • Donaldson C J, Sutton SW, Perrin MH, et al Cloning and characterization of human urocortin Endrocrinology 1996;137:2167-70
    • (1996) Endrocrinology , vol.137 , pp. 2167-2170
    • Donaldson, C.J.1    Sutton, S.W.2    Perrin, M.H.3
  • 5
    • 0035956938 scopus 로고    scopus 로고
    • Urocortin II: A member of the corticotropin-releasing factor (CRF) neuropeptide family that is selectively bound by type 2 CRF receptors
    • Reyes TM, Lewis K, Perrin MH, et al Urocortin II: a member of the corticotropin-releasing factor (CRF) neuropeptide family that is selectively bound by type 2 CRF receptors Proc Natl Acad Sci USA 2001;98:2843-8
    • (2001) Proc Natl Acad Sci USA , vol.98 , pp. 2843-2848
    • Reyes, T.M.1    Lewis, K.2    Perrin, M.H.3
  • 6
    • 0035912712 scopus 로고    scopus 로고
    • Identification of urocortin III, an additional member of the corticotropin-releasing factor (CRF) family with high affinity for the CRF2 receptor
    • Lewis K, Perrin MH, Blount A, et al Identification of urocortin III, an additional member of the corticotropin-releasing factor (CRF) family with high affinity for the CRF2 receptor Proc Natl Acad Sci USA 2001;98:7570-5
    • (2001) Proc Natl Acad Sci USA , vol.98 , pp. 7570-7575
    • Lewis, K.1    Perrin, M.H.2    Blount, A.3
  • 7
    • 77952549409 scopus 로고    scopus 로고
    • Progress in corticotropin-releasing factor-1 antagonist development
    • Zorrilla EP, Koob GF Progress in corticotropin-releasing factor-1 antagonist development Drug Discov Today 2010;15:371-83
    • (2010) Drug Discov Today , vol.15 , pp. 371-383
    • Zorrilla, E.P.1    Koob, G.F.2
  • 8
    • 65649144676 scopus 로고    scopus 로고
    • Corticotropin-releasing factor receptor antagonists
    • Gilligan PJ Corticotropin-releasing factor receptor antagonists Expert Opin Ther Patents 2006;16:913-24
    • (2006) Expert Opin Ther Patents , vol.16 , pp. 913-924
    • Gilligan, P.J.1
  • 9
    • 53049106905 scopus 로고    scopus 로고
    • Recent advances in corticotropin-releasing factor receptor antagonists
    • Dzierba CD, Hartz RA, Bronson JJ Recent advances in corticotropin- releasing factor receptor antagonists Annu Rep Med Chem 2008;43:3-19
    • (2008) Annu Rep Med Chem , vol.43 , pp. 3-19
    • Dzierba, C.D.1    Hartz, R.A.2    Bronson, J.J.3
  • 11
    • 0034193881 scopus 로고    scopus 로고
    • Effects of the high-affinity corticotropinreleasing hormone receptor 1 antagonist R121919 in major depression: The first 20 patients treated
    • Zobel AW, Nickel T, Kunzel HE, et al Effects of the high-affinity corticotropinreleasing hormone receptor 1 antagonist R121919 in major depression: the first 20 patients treated J Psychiatr Res 2000;34:171-81
    • (2000) J Psychiatr Res , vol.34 , pp. 171-181
    • Zobel, A.W.1    Nickel, T.2    Kunzel, H.E.3
  • 12
    • 34547907098 scopus 로고    scopus 로고
    • High-affinity CRF (1) receptor antagonist NBI-34041: Preclinical and clinical data suggest safety and efficacy in attenuating elevated stress response
    • Ising M, Zimmerman US, Kunzel HE, et al High-affinity CRF (1) receptor antagonist NBI-34041: preclinical and clinical data suggest safety and efficacy in attenuating elevated stress response Neuropsychopharmacology 2007;32:1941-9
    • (2007) Neuropsychopharmacology , vol.32 , pp. 1941-1949
    • Ising, M.1    Zimmerman, U.S.2    Kunzel, H.E.3
  • 13
    • 43949134527 scopus 로고    scopus 로고
    • A 6-week randomized, placebo-controlled trial of CP-316,311 (a selective CRH1 antagonist) in the treatment ofmajor depression
    • Binneman B, Feltner D, Kolluri S, et al A 6-week randomized, placebo-controlled trial of CP-316,311 (a selective CRH1 antagonist) in the treatment ofmajor depression Am J Pyschiatry 2008;165:617-20
    • (2008) Am J Pyschiatry , vol.165 , pp. 617-620
    • Binneman, B.1    Feltner, D.2    Kolluri, S.3
  • 14
    • 84880668509 scopus 로고    scopus 로고
    • Neurocrine Announces Top-Line Results of Corticotropin Releasing Factor Antagonist GSK561679 for Treatment of Major Depressive Disorder[Last accessed 22 February 2013]
    • Neurocrine Announces Top-Line Results of Corticotropin Releasing Factor Antagonist GSK561679 for Treatment of Major Depressive Disorder Neurocrine Biosciences press release 2010 Available from: www.neurocrine com [Last accessed 22 February 2013]
    • (2010) Neurocrine Biosciences Press Release
  • 15
    • 77953525393 scopus 로고    scopus 로고
    • Multicenter, randomized, double-blind, active comparator and placebo-controlled trial of a corticotropin-releasing factor receptor-1 antagonist in generalized anxiety disorder
    • Coric V, Feldman HH, Oren DA, et al Multicenter, randomized, double-blind, active comparator and placebo-controlled trial of a corticotropin-releasing factor receptor-1 antagonist in generalized anxiety disorder Depress Anxiety 2010;27:417-25
    • (2010) Depress Anxiety , vol.27 , pp. 417-425
    • Coric, V.1    Feldman, H.H.2    Oren, D.A.3
  • 16
    • 84880666475 scopus 로고    scopus 로고
    • Evaluation of GSK561679 in Women with Post-Traumatic Stress Disorder [Last accessed 22 February 2013] Clincaltrials.gov Identifier NCT01018992
    • Evaluation of GSK561679 in Women with Post-Traumatic Stress Disorder Clincaltrials.gov identifier NCT01018992 Available from: clinicaltrials.gov [Last accessed 22 February 2013]
  • 18
    • 84880651636 scopus 로고    scopus 로고
    • Pexacerfont for Stress-induced Food Craving[Last accessed 22 February Identifier NCT01656577
    • Pexacerfont for Stress-induced Food Craving Clincaltrials.gov identifier NCT01656577 Available from: clinicaltrials.gov [Last accessed 22 February 2013]
    • (2013) Clincaltrials.gov
  • 19
    • 84878227722 scopus 로고    scopus 로고
    • Pexacerfont to Rduce Stress-induced Tobacco Craving.,Last accessed 22 February
    • Pexacerfont to Reduce Stress-induced Tobacco Craving Clinicaltrials.gov identifier NCT01557556 Available from: clinicaltrials.gov [Last accessed 22 February 2013]
    • (2013) Clinicaltrials.gov Identifier NCT01557556
  • 20
    • 84878227722 scopus 로고    scopus 로고
    • Corticotropin-Releasing Hormone Receptor 1 (CRH1) Antagonism in Anxious Alcoholics[Last accessed 22 February
    • Corticotropin-Releasing Hormone Receptor 1 (CRH1) Antagonism in Anxious Alcoholics Clinicaltrials.gov identifier NCT01227980 Available from: clinicaltrials.gov [Last accessed 22 February 2013]
    • (2013) Clinicaltrials.gov Identifier NCT01227980
  • 21
    • 0033168446 scopus 로고    scopus 로고
    • Pharmacophore development for corticotropin-releasing hormone: New insights into inhibitor activity
    • Keller PA, Bowman M, Dang KH, et al Pharmacophore development for corticotropin-releasing hormone: new insights into inhibitor activity J Med Chem 1999;42:2351-7
    • (1999) J Med Chem , vol.42 , pp. 2351-2357
    • Keller, P.A.1    Bowman, M.2    Dang, K.H.3
  • 22
    • 24744435144 scopus 로고    scopus 로고
    • Design and synthesis of tricyclic corticotropin-releasing factor-1 antagonists
    • Gross RS, Guo Z, Dyck B, et al Design and synthesis of tricyclic corticotropin-releasing factor-1 antagonists J Med Chem 2005;48:5780-93
    • (2005) J Med Chem , vol.48 , pp. 5780-5793
    • Gross, R.S.1    Guo, Z.2    Dyck, B.3
  • 27
    • 80052921582 scopus 로고    scopus 로고
    • Discovery of potent, metabolically stable purine CRF-1 antagonists with differentiated binding kinetic profiles
    • Miller DC, Klute W, Brown AD Discovery of potent, metabolically stable purine CRF-1 antagonists with differentiated binding kinetic profiles Bioorg Med Chem Lett 2011;21:6108-11
    • (2011) Bioorg Med Chem Lett , vol.21 , pp. 6108-6111
    • Miller, D.C.1    Klute, W.2    Brown, A.D.3
  • 28
    • 84859956726 scopus 로고    scopus 로고
    • Binding kinetics redefine the antagonist pharmacology of the corticotropin-releasing factor type 1 receptor
    • Fleck BA, Hoare SRJ, Pick RR, et al Binding kinetics redefine the antagonist pharmacology of the corticotropin-releasing factor type 1 receptor J Pharmacol Exp Ther 2012;341:518-31
    • (2012) J Pharmacol Exp Ther , vol.341 , pp. 518-531
    • Fleck, B.A.1    Hoare, S.R.J.2    Pick, R.R.3
  • 31
    • 84880654652 scopus 로고    scopus 로고
    • SB Pharmaco Puerto Rico, Inc Neurocrine Biosciences, Inc WO2006044821
    • SB Pharmaco Puerto Rico, Inc Neurocrine Biosciences, Inc CRF receptor antagonists and methods relating thereto WO2006044821; 2006
    • (2006) CRF Receptor Antagonists and Methods Relating Thereto
  • 34
    • 33847772007 scopus 로고    scopus 로고
    • 3-(4-Chloro-2-morpholin-4-ylthiazol-5-yl)-8-(1-ethylpropyl)-2, 6-dimethyl-imidazo[1,2-b]pyridizine: A novel brain-penetrant, orally available corticotropin-releasing factor receptor 1 antagonist with efficacy in animal models of alcoholism
    • Gehlert DR, Cippitelli A, Thorsell A, et al 3-(4-Chloro-2-morpholin-4- ylthiazol-5-yl)-8-(1-ethylpropyl)-2,6-dimethyl-imidazo[1,2-b]pyridizine: a novel brain-penetrant, orally available corticotropin-releasing factor receptor 1 antagonist with efficacy in animal models of alcoholism J Neurosci 2007;27:2718-26
    • (2007) J Neurosci , vol.27 , pp. 2718-2726
    • Gehlert, D.R.1    Cippitelli, A.2    Thorsell, A.3
  • 36
    • 84880655960 scopus 로고    scopus 로고
    • Eisai R&D Management Co WO2011043387
    • Eisai R&D Management Co Pyrazoloxazole compound WO2011043387; 2011
    • (2011) Pyrazoloxazole Compound
  • 39
    • 84880670652 scopus 로고    scopus 로고
    • Eisai R&D Management Co WO2011043381
    • Eisai R&D Management Co Pyrazolothiazole compound WO2011043381; 2011
    • (2011) Pyrazolothiazole Compound
  • 41
    • 84867378507 scopus 로고    scopus 로고
    • Design, synthesis, and structure-activity relationships of novel pyrazolo[5,1-b]thiazole derivatives as potent and orally active corticotropin-releasing factor 1 receptor antagonists
    • Takahashi Y, Hashizume M, Shin K, et al Design, synthesis, and structure-activity relationships of novel pyrazolo[5,1-b]thiazole derivatives as potent and orally active corticotropin-releasing factor 1 receptor antagonists J Med Chem 2012;55:8450-63
    • (2012) J Med Chem , vol.55 , pp. 8450-8463
    • Takahashi, Y.1    Hashizume, M.2    Shin, K.3
  • 44
    • 72249097682 scopus 로고    scopus 로고
    • A strategy to minimize reactive metabolite formation: Discovery of (S)-4-(1-cyclopropyl-2-methoxyethyl)-6-[6-(difluoromethoxy)-2, 5-dimethylpyridin-3-ylamino]-5-oxo-4,5-dihydropyrazine-2-carbonitrile as a potent, orally bioavailable corticotropin-releasing factor-1 receptor antagonist
    • Hartz RA, Ahuja VT, Zhuo X, et al A strategy to minimize reactive metabolite formation: discovery of (S)-4-(1-cyclopropyl-2-methoxyethyl)-6-[6- (difluoromethoxy)-2,5-dimethylpyridin-3-ylamino]-5-oxo-4,5-dihydropyrazine-2- carbonitrile as a potent, orally bioavailable corticotropin-releasing factor-1 receptor antagonist J Med Chem 2009;52:7653-68
    • (2009) J Med Chem , vol.52 , pp. 7653-7668
    • Hartz, R.A.1    Ahuja, V.T.2    Zhuo, X.3
  • 46
    • 0029862077 scopus 로고    scopus 로고
    • Rapid microscale synthesis, a new method for lead optimization using robotics and solution phase chemistry: Application to the synthesis and optimization of corticotropin-releasingfactor1 receptor antagonists
    • Whitten JP, Xie YF, Erickson PE, et al Rapid microscale synthesis, a new method for lead optimization using robotics and solution phase chemistry: application to the synthesis and optimization of corticotropin-releasingfactor1 receptor antagonists J Med Chem 1996;39:4354-7
    • (1996) J Med Chem , vol.39 , pp. 4354-4357
    • Whitten, J.P.1    Xie, Y.F.2    Erickson, P.E.3
  • 47
    • 80052600644 scopus 로고    scopus 로고
    • 6-7-Dihydro-5H-cyclopenta[d]pyrazolo[1,5-A] pyrimidines and their derivatives as novel corticotropin-releasing factor 1 receptor antagonists
    • Saito T, Obitsu T, Kondo T, et al 6-7-Dihydro-5H-cyclopenta[d]pyrazolo[1, 5-A] pyrimidines and their derivatives as novel corticotropin-releasing factor 1 receptor antagonists Bioorg Med Chem 2011;19:5432-45
    • (2011) Bioorg Med Chem , vol.19 , pp. 5432-5445
    • Saito, T.1    Obitsu, T.2    Kondo, T.3
  • 48
    • 80053242747 scopus 로고    scopus 로고
    • Pyrazolo[1,5-A]pyrimidines, triazolo[1,5-A]pyrimidines and their tricyclic derivatives as corticotropin-releasing factor 1 (CRF1) receptor antagonists
    • Saito T, Obitsu T, Minamoto C, et al Pyrazolo[1,5-A]pyrimidines, triazolo[1,5-A]pyrimidines and their tricyclic derivatives as corticotropin-releasing factor 1 (CRF1) receptor antagonists Bioorg Med Chem 2011;19:5955-66
    • (2011) Bioorg Med Chem , vol.19 , pp. 5955-5966
    • Saito, T.1    Obitsu, T.2    Minamoto, C.3
  • 49
  • 50
    • 84880658615 scopus 로고    scopus 로고
    • Takeda Pharmaceutical Co Ltd US20090186879
    • Takeda Pharmaceutical Co Ltd Tricyclic compounds and use thereof US20090186879; 2009
    • (2009) Tricyclic Compounds and Use Thereof
  • 51
    • 84880648573 scopus 로고    scopus 로고
    • Takeda Pharmaceutical Co Ltd. WO2006116412
    • Takeda Pharmaceutical Co Ltd Fused heterocyclic compounds WO2006116412; 2006
    • (2006) Fused Heterocyclic Compounds
  • 52
    • 84863483160 scopus 로고    scopus 로고
    • Design, synthesis and structure-activity relationships of 5-alkylaminolquinolines as a novel series of CRF1 receptor antagonists
    • Takeda K, Terauchi T, Shin K, et al Design, synthesis and structure-activity relationships of 5-alkylaminolquinolines as a novel series of CRF1 receptor antagonists Bioorg Med Chem Lett 2012;22:4756-61
    • (2012) Bioorg Med Chem Lett , vol.22 , pp. 4756-4761
    • Takeda, K.1    Terauchi, T.2    Shin, K.3
  • 53
    • 84930251481 scopus 로고    scopus 로고
    • Takeda Pharmaceutical Co Ltd. WO2008051533
    • Takeda Pharmaceutical Co Ltd Benzimidazole compounds WO2008051533; 2008
    • (2008) Benzimidazole Compounds
  • 56
    • 84880650331 scopus 로고    scopus 로고
    • A trial evaluating the efficacy and tolerability of SSR125543 in outpatients with major depressive disorder (AGATE) [Last accessed 22 February
    • A trial evaluating the efficacy and tolerability of SSR125543 in outpatients with major depressive disorder (AGATE) Clincaltrials.gov identifier NCT01034995 Available from: clinicaltrials.gov [Last accessed 22 February 2013]
    • (2013) Clincaltrials.gov Identifier NCT01034995
  • 57
    • 48649099526 scopus 로고    scopus 로고
    • 2-Arylpyrimidines: Novel CRF1 receptor antagonists
    • Yoon T, De Lombaert S, Brodbeck R, et al 2-Arylpyrimidines: novel CRF1 receptor antagonists Bioorg Med Chem Lett 2008;18:4486-90
    • (2008) Bioorg Med Chem Lett , vol.18 , pp. 4486-4490
    • Yoon, T.1    De Lombaert, S.2    Brodbeck, R.3
  • 58
    • 84880666133 scopus 로고    scopus 로고
    • Ono Pharmaceutical Co WO2007069565
    • Ono Pharmaceutical Co Bicyclic heterocyclic compound WO2007069565; 2007
    • (2007) Bicyclic Heterocyclic Compound
  • 59
    • 84880666133 scopus 로고    scopus 로고
    • Ono Pharmaceutical Co WO2007069671
    • Ono Pharmaceutical Co Bicyclic heterocyclic compound WO2007069671; 2007
    • (2007) Bicyclic Heterocyclic Compound
  • 60
    • 84880672666 scopus 로고    scopus 로고
    • Ono Pharmaceutical Co WO2008136377
    • Ono Pharmaceutical Co Bicyclic heterocyclic compound WO2008136377; 2008
    • (2008) Bicyclic Heterocyclic Compound
  • 61
    • 84865128033 scopus 로고    scopus 로고
    • Design, synthesis and structure-activity relationships of a series of 2-Ar-8-methyl-5-alkylaminoquinolines as novel CRF1 receptor antagonists
    • Takeda K, Teruachi T, Hashizume M, et al Design, synthesis and structure-activity relationships of a series of 2-Ar-8-methyl-5- alkylaminoquinolines as novel CRF1 receptor antagonists Bioorg Med Chem Lett 2012;22:5372-8
    • (2012) Bioorg Med Chem Lett , vol.22 , pp. 5372-5378
    • Takeda, K.1    Teruachi, T.2    Hashizume, M.3
  • 63
    • 84855809718 scopus 로고    scopus 로고
    • Pyrrolo[1,2-b]pyridazines, pyrrolo[2,1-f] triazine-(3H)-ones, and related compounds as novel corticotropin-releasing factor 1 (CRF1) receptor antagonists
    • Saito T, Obitsu T, Kohno H, et al Pyrrolo[1,2-b]pyridazines, pyrrolo[2,1-f] triazine-(3H)-ones, and related compounds as novel corticotropin-releasing factor 1 (CRF1) receptor antagonists Bioorg Med Chem 2012;20:1122-38
    • (2012) Bioorg Med Chem , vol.20 , pp. 1122-1138
    • Saito, T.1    Obitsu, T.2    Kohno, H.3
  • 66
    • 0037161584 scopus 로고    scopus 로고
    • Arylamidrazones as novel corticotropin releasing factor receptor antagonists
    • Wilson DM, Termin AP, Mao L, et al Arylamidrazones as novel corticotropin releasing factor receptor antagonists J Med Chem 2002;45:2123-6
    • (2002) J Med Chem , vol.45 , pp. 2123-2126
    • Wilson, D.M.1    Termin, A.P.2    Mao, L.3
  • 67
    • 2342557320 scopus 로고    scopus 로고
    • N-Phenylphenylglycines as novel corticotropin releasing factor receptor antagonists
    • Molteni V, Penzotti J, Wilson DM, et al N-Phenylphenylglycines as novel corticotropin releasing factor receptor antagonists J Med Chem 2004;47:2426-9
    • (2004) J Med Chem , vol.47 , pp. 2426-2429
    • Molteni, V.1    Penzotti, J.2    Wilson, D.M.3
  • 68
    • 27744493219 scopus 로고    scopus 로고
    • Corticotropin-releasing hormone receptor 1 antagonist blocks brain-gut activation induced by colonic distension in rats
    • Saito K, Kasai T, Nagura Y, et al Corticotropin-releasing hormone receptor 1 antagonist blocks brain-gut activation induced by colonic distension in rats Gastroenterology 2005;129:1533-43
    • (2005) Gastroenterology , vol.129 , pp. 1533-1543
    • Saito, K.1    Kasai, T.2    Nagura, Y.3
  • 72
    • 79952636158 scopus 로고    scopus 로고
    • Corticotropin releasing factor receptor antagonists for major depressive disorder
    • Paez-Pareda M, Hausch F, Holsboer F Corticotropin releasing factor receptor antagonists for major depressive disorder Expert Opin Investig Drugs 2011;20:519-35
    • (2011) Expert Opin Investig Drugs , vol.20 , pp. 519-535
    • Paez-Pareda, M.1    Hausch, F.2    Holsboer, F.3
  • 73
    • 84856105751 scopus 로고    scopus 로고
    • Update on corticotropin-releasing factor pharmacotherapy for psychiatric disorders: A revisionist view
    • Koob G, Zorrilla EP Update on corticotropin-releasing factor pharmacotherapy for psychiatric disorders: a revisionist view Neuropsychopharmacology 2012;37:308-9
    • (2012) Neuropsychopharmacology , vol.37 , pp. 308-309
    • Koob, G.1    Zorrilla, E.P.2
  • 74
    • 16244383540 scopus 로고    scopus 로고
    • Mechanisms of peptide and nonpeptide ligand binding to class B G-protein-coupled receptors
    • Hoare SRJ Mechanisms of peptide and nonpeptide ligand binding to class B G-protein-coupled receptors Drug Discov Today 2005;10:417-27
    • (2005) Drug Discov Today , vol.10 , pp. 417-427
    • Srj, H.1
  • 75
    • 0034127008 scopus 로고    scopus 로고
    • Mice deficient for corticotropin-releasing hormone receptor-2 display anxiety-like behaviour and are hypersensitive to stress
    • Bale TL, Contarino A, Smith GW, et al Mice deficient for corticotropin-releasing hormone receptor-2 display anxiety-like behaviour and are hypersensitive to stress Nat Genet 2000;24:410-14
    • (2000) Nat Genet , vol.24 , pp. 410-414
    • Bale, T.L.1    Contarino, A.2    Smith, G.W.3
  • 76
    • 17944379995 scopus 로고    scopus 로고
    • Regulation of the hypothalamic-pituitary-adrenocortical system in mice deficient for CRH receptors 1 and2
    • Preil J, Muller MB, Gesing A, et al Regulation of the hypothalamic-pituitary-adrenocortical system in mice deficient for CRH receptors 1 and2 Endocrinology 2001;142:4946-55
    • (2001) Endocrinology , vol.142 , pp. 4946-4955
    • Preil, J.1    Muller, M.B.2    Gesing, A.3
  • 77
    • 84873095820 scopus 로고    scopus 로고
    • Something's got to give: Psychiatric disease on the rise and novel drug development on the decline
    • Chandler DJ Something's got to give: psychiatric disease on the rise and novel drug development on the decline Drug Discov Today 2013;18:202-6
    • (2013) Drug Discov Today , vol.18 , pp. 202-206
    • Chandler, D.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.