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Volumn 23, Issue 1, 2013, Pages 31-45

Phosphodiesterase 10A inhibitors: A 2009 - 2012 patent update

Author keywords

Antipsychotic; Basal ganglia; Huntington's disease; Medium spiny neuron; Negative symptom; PDE10A; Phosphodiesterase 10A; Pro cognitive; Schizophrenia; Striatum

Indexed keywords

2 [4 [1 METHYL 4 (4 PYRIDINYL) 3 PYRAZOLYL]PHENOXYMETHYL]QUINOLINE; MP-10; PHOSPHODIESTERASE 10A INHIBITOR; PHOSPHODIESTERASE INHIBITOR; RADIOLIGAND; TAK 063; UNCLASSIFIED DRUG;

EID: 84871523977     PISSN: 13543776     EISSN: 17447674     Source Type: Journal    
DOI: 10.1517/13543776.2012.739157     Document Type: Review
Times cited : (33)

References (95)
  • 1
    • 84857080656 scopus 로고    scopus 로고
    • Cyclic nucleotide phosphodiesterase (PDE) isozymes as targets of the intracellular signalling network: Benefits of PDE inhibitors in various diseases and perspectives for future therapeutic developments
    • Keravis T, Lugnier C. Cyclic nucleotide phosphodiesterase (PDE) isozymes as targets of the intracellular signalling network: benefits of PDE inhibitors in various diseases and perspectives for future therapeutic developments. Br J Pharmacol 2012;165:1288-305
    • (2012) Br J Pharmacol , vol.165 , pp. 1288-1305
    • Keravis, T.1    Lugnier, C.2
  • 2
    • 79955664087 scopus 로고    scopus 로고
    • Mammalian cyclic nucleotide phosphodiesterases: Molecular mechanisms and physiological functions
    • Francis SH, Blount MA, Corbin JD. Mammalian cyclic nucleotide phosphodiesterases: molecular mechanisms and physiological functions. Physiol Rev 2011;91:651-90
    • (2011) Physiol Rev , vol.91 , pp. 651-690
    • Francis, S.H.1    Blount, M.A.2    Corbin, J.D.3
  • 3
    • 79953296930 scopus 로고    scopus 로고
    • PDE10A inhibitors: Novel therapeutic drugs for schizophrenia
    • Kehler J, Nielsen J. PDE10A inhibitors: novel therapeutic drugs for schizophrenia. Curr Pharm Des 2011;17:137-50
    • (2011) Curr Pharm des , vol.17 , pp. 137-150
    • Kehler, J.1    Nielsen, J.2
  • 4
    • 84866336121 scopus 로고    scopus 로고
    • Current Landscape of Phosphodiesterase 10A (PDE10A) Inhibition
    • Chappie TA, Helal CJ, Hou X. Current Landscape of Phosphodiesterase 10A (PDE10A) Inhibition. J Med Chem 2012;55(17):7299-331
    • (2012) J Med Chem , vol.55 , Issue.17 , pp. 7299-7331
    • Chappie, T.A.1    Helal, C.J.2    Hou, X.3
  • 6
    • 33847022578 scopus 로고    scopus 로고
    • The potential therapeutic use of phosphodiesterase 10 inhibitors
    • Kehler Jan, Ritzen A, Greve DR. The potential therapeutic use of phosphodiesterase 10 inhibitors. Expert Opin Ther Patents 2007;17:147-58
    • (2007) Expert Opin Ther Patents , vol.17 , pp. 147-158
    • Jan, K.1    Ritzen, A.2    Greve, D.R.3
  • 15
    • 78650751009 scopus 로고    scopus 로고
    • Synthesis and SAR study of new phenylimidazole-pyrazolo[1,5-c] quinazolines as potent phosphodiesterase 10A inhibitors
    • Asproni B, Murineddu G, Pau A. Synthesis and SAR study of new phenylimidazole-pyrazolo[1,5-c] quinazolines as potent phosphodiesterase 10A inhibitors. Bioorg Med Chem 2011;19:642-9
    • (2011) Bioorg Med Chem , Issue.19 , pp. 642-649
    • Asproni, B.1    Murineddu, G.2    Pau, A.3
  • 16
    • 79957805368 scopus 로고    scopus 로고
    • Triazoloquinazolines as a novel class of phosphodiesterase 10A (PDE10A) inhibitors
    • Kehler J, Ritzen A, Langgard M. Triazoloquinazolines as a novel class of phosphodiesterase 10A (PDE10A) inhibitors. Bioorg Med Chem Lett 2011;21:3738-42
    • (2011) Bioorg Med Chem Lett , Issue.21 , pp. 3738-3742
    • Kehler, J.1    Ritzen, A.2    Langgard, M.3
  • 19
    • 84865451685 scopus 로고    scopus 로고
    • Discovery of tetrahydropyridopyrimidine phosphodiesterase 10A inhibitors for the treatment of schizophrenia
    • Raheem IT, Breslin MJ, Fandozzi C, et al. Discovery of tetrahydropyridopyrimidine phosphodiesterase 10A inhibitors for the treatment of schizophrenia. Bioorg Med Chem Lett 2012;22(18):5903-8
    • (2012) Bioorg Med Chem Lett , vol.22 , Issue.18 , pp. 5903-5908
    • Raheem, I.T.1    Breslin, M.J.2    Fandozzi, C.3
  • 20
    • 84866379713 scopus 로고    scopus 로고
    • The novel phosphodiesterase 10a inhibitor thpp-1has antipsychotic-like effects in rat and improves cognition in rat and rhesus monkey
    • Smith SM, Uslanerb JM, Cox CD, et al. The novel phosphodiesterase 10A inhibitor THPP-1has antipsychotic-like effects in rat and improves cognition in rat and rhesus monkey. Neuropharmacology 2013;64(1):215-23
    • (2013) Neuropharmacology , vol.64 , Issue.1 , pp. 215-223
    • Smith, S.M.1    Uslanerb, J.M.2    Cox, C.D.3
  • 21
    • 84871528548 scopus 로고    scopus 로고
    • Merck. WO2011022213; 2011
    • Merck. WO2011022213; 2011
  • 22
    • 84871524337 scopus 로고    scopus 로고
    • Merck. WO2010138585; 2010
    • Merck. WO2010138585; 2010
  • 23
    • 84871509656 scopus 로고    scopus 로고
    • Merck. WO2011053559; 2011
    • Merck. WO2011053559; 2011
  • 24
    • 84871521194 scopus 로고    scopus 로고
    • Merck. WO2012044561; 2012
    • Merck. WO2012044561; 2012
  • 25
    • 84871504227 scopus 로고    scopus 로고
    • Merck. WO2012044562; 2012
    • Merck. WO2012044562; 2012
  • 26
    • 84871483357 scopus 로고    scopus 로고
    • Merck. WO2012054366; 2012
    • Merck. WO2012054366; 2012
  • 27
    • 84871493105 scopus 로고    scopus 로고
    • Merck. WO2012058133; 2012
    • Merck. WO2012058133; 2012
  • 28
    • 84871486929 scopus 로고    scopus 로고
    • Merck (Schering Corp.). WO2010062559; 2010
    • Merck (Schering Corp.). WO2010062559; 2010
  • 29
    • 84856211546 scopus 로고    scopus 로고
    • Pyrazoloquinolines as PDE10A inhibitors: Discovery of a tool compound
    • McElroy WT, Tan Z, Basu K, et al. Pyrazoloquinolines as PDE10A inhibitors: discovery of a tool compound. Bioorg Med Chem Lett 2012;22:1335-9
    • (2012) Bioorg Med Chem Lett , Issue.22 , pp. 1335-1339
    • McElroy, W.T.1    Tan, Z.2    Basu, K.3
  • 30
    • 84855681654 scopus 로고    scopus 로고
    • The discovery of potent, selective, and orally active pyrazoloquinolines as PDE10A inhibitors for the treatment of Schizophrenia
    • Ho GD, Yang S-W, Smotryski J, et al. The discovery of potent, selective, and orally active pyrazoloquinolines as PDE10A inhibitors for the treatment of Schizophrenia. Bioorg Med Chem Lett 2012;22:1019-22
    • (2012) Bioorg Med Chem Lett , Issue.22 , pp. 1019-1022
    • Ho, G.D.1    Yang, S.-W.2    Smotryski, J.3
  • 31
    • 84655170136 scopus 로고    scopus 로고
    • Discovery of orally active pyrazoloquinolines as potent PDE10 inhibitors for the management of schizophrenia
    • Yang S-W, Smotryski J, McElroy WT, et al. Discovery of orally active pyrazoloquinolines as potent PDE10 inhibitors for the management of schizophrenia. Bioorg Med Chem Lett 2012;22:235-9
    • (2012) Bioorg Med Chem Lett , Issue.22 , pp. 235-239
    • Yang, S.-W.1    Smotryski, J.2    McElroy, W.T.3
  • 34
    • 84862826287 scopus 로고    scopus 로고
    • The SAR development of dihydroimidazoisoquinoline derivatives as phosphodiesterase 10A inhibitors for the treatment of schizophrenia
    • Ho GD, Seganish MW, Bercovici A, et al. The SAR development of dihydroimidazoisoquinoline derivatives as phosphodiesterase 10A inhibitors for the treatment of schizophrenia. Bioorg Med Chem Lett 2012;22: 2585-9
    • (2012) Bioorg Med Chem Lett , Issue.22 , pp. 2585-2589
    • Ho, G.D.1    Seganish, M.W.2    Bercovici, A.3
  • 35
    • 84871505159 scopus 로고    scopus 로고
    • WO2009143178
    • Omeros Corp. WO2009143178; 2009
    • (2009) Omeros Corp
  • 36
    • 84871504041 scopus 로고    scopus 로고
    • WO2010017236
    • Omeros Corp. WO2010017236; 2010
    • (2010) Omeros Corp
  • 38
    • 84865133568 scopus 로고    scopus 로고
    • Novel 2-methoxyacylhydrazones as potent, selective PDE10A inhibitors with activity in animal models of schizophrenia
    • Cutshall NS, Onrust R, Rohde A, et al. Novel 2-methoxyacylhydrazones as potent, selective PDE10A inhibitors with activity in animal models of schizophrenia. Bioorg Med Chem Lett 2012;22:5595-9
    • (2012) Bioorg Med Chem Lett , Issue.22 , pp. 5595-5599
    • Cutshall, N.S.1    Onrust, R.2    Rohde, A.3
  • 39
    • 84871523288 scopus 로고    scopus 로고
    • Omeros Corp. WO2011112828; 2011
    • Omeros Corp. WO2011112828; 2011
  • 40
    • 84871525888 scopus 로고    scopus 로고
    • Envivo Pharmaceuticals, Inc. WO2009158473; 2009
    • Envivo Pharmaceuticals, Inc. WO2009158473; 2009
  • 41
    • 84871494165 scopus 로고    scopus 로고
    • Envivo Pharmaceuticals, Inc. WO2009158393; 2009
    • Envivo Pharmaceuticals, Inc. WO2009158393; 2009
  • 42
    • 84871526735 scopus 로고    scopus 로고
    • Envivo Pharmaceuticals, Inc. WO2009158467; 2009
    • Envivo Pharmaceuticals, Inc. WO2009158467; 2009
  • 43
    • 84871476555 scopus 로고    scopus 로고
    • Envivo Pharmaceuticals, Inc. WO2010006130; 2010
    • Envivo Pharmaceuticals, Inc. WO2010006130; 2010
  • 44
    • 84871522981 scopus 로고    scopus 로고
    • F. Hoffmann-La Roche AG. WO2010063610; 2010
    • F. Hoffmann-La Roche AG. WO2010063610; 2010
  • 45
    • 84871499432 scopus 로고    scopus 로고
    • F. Hoffmann-La Roche AG. WO2010094762; 2010
    • F. Hoffmann-La Roche AG. WO2010094762; 2010
  • 46
    • 84871510169 scopus 로고    scopus 로고
    • F. Hoffmann-La Roche AG. US20110071128; 2011
    • F. Hoffmann-La Roche AG. US20110071128; 2011
  • 47
    • 84871475933 scopus 로고    scopus 로고
    • F. Hoffmann-La Roche AG. WO2011117264; 2011
    • F. Hoffmann-La Roche AG. WO2011117264; 2011
  • 48
    • 84871517775 scopus 로고    scopus 로고
    • F. Hoffmann-La Roche AG. US20120142665; 2012
    • F. Hoffmann-La Roche AG. US20120142665; 2012
  • 49
    • 84871488982 scopus 로고    scopus 로고
    • AG. WO2011089132
    • F. Hoffmann-La Roche AG. WO2011089132; 2011
    • (2011)
    • Hoffmann-La, F.1
  • 50
    • 84871530280 scopus 로고    scopus 로고
    • F. Hoffmann-La Roche AG. WO2011154327; 2011
    • F. Hoffmann-La Roche AG. WO2011154327; 2011
  • 51
    • 84871528102 scopus 로고    scopus 로고
    • WO2010138833
    • Biotie/Wyeth. WO2010138833; 2010
    • (2010)
    • Wyeth, B.1
  • 52
    • 80455140545 scopus 로고    scopus 로고
    • Highly potent, selective, and orally active phosphodiesterase 10A inhibitors
    • Malamas MS, Ni Y, Erdei J, et al. Highly potent, selective, and orally active phosphodiesterase 10A inhibitors. J Med Chem 2011;54:7621-38
    • (2011) J Med Chem , Issue.54 , pp. 7621-7638
    • Malamas, M.S.1    Ni, Y.2    Erdei, J.3
  • 53
    • 84871525458 scopus 로고    scopus 로고
    • Biotie/Wyeth. WO2010054260; 2010
    • Biotie/Wyeth. WO2010054260; 2010
  • 54
    • 84871525769 scopus 로고    scopus 로고
    • Biotie/Wyeth. WO2010054253; 2010
    • Biotie/Wyeth. WO2010054253; 2010
  • 55
    • 77953206436 scopus 로고    scopus 로고
    • Discovery of Imidazo [1,5-A]pyrido[3,2-e] pyrazines as a new class ofphosphodiesterase 10A inhibitors
    • Hofgen N, Stange H, Schindler R, et al. Discovery of Imidazo[1,5-a] pyrido[3,2-e] pyrazines as a new class ofphosphodiesterase 10A inhibitors. J Med Chem 2010;5: 4399-411
    • (2010) J Med Chem , vol.5 , pp. 4399-4411
    • Hofgen, N.1    Stange, H.2    Schindler, R.3
  • 56
    • 84871512260 scopus 로고    scopus 로고
    • Biocrea/Boehringer Ingelheim. WO2012104293; 2012
    • Biocrea/Boehringer Ingelheim. WO2012104293; 2012
  • 57
    • 84871498213 scopus 로고    scopus 로고
    • Glenmark Pharmaceuticals Ltd WO2011132048 2011
    • Glenmark Pharmaceuticals Ltd. WO2011132048; 2011
  • 58
    • 84871509212 scopus 로고    scopus 로고
    • Glenmark Pharmaceuticals Ltd WO2011138657, 2011
    • Glenmark Pharmaceuticals Ltd. WO2011138657; 2011
  • 59
    • 84871520843 scopus 로고    scopus 로고
    • Glenmark Pharmaceuticals Ltd WO2011132051 2011
    • Glenmark Pharmaceuticals Ltd. WO2011132051; 2011
  • 60
    • 84871505348 scopus 로고    scopus 로고
    • Glenmark Pharmaceuticals Ltd IN2009MU03042 2012
    • Glenmark Pharmaceuticals Ltd. IN2009MU03042; 2012
  • 61
    • 84871476586 scopus 로고    scopus 로고
    • Takeda Pharmaceutical Co. Ltd. US20100197651, 2010
    • Takeda Pharmaceutical Co. Ltd. US20100197651; 2010
  • 62
    • 84871517680 scopus 로고    scopus 로고
    • Takeda Pharmaceutical Co. Ltd. WO2012018059; 2012
    • Takeda Pharmaceutical Co. Ltd. WO2012018059; 2012
  • 63
    • 84871497095 scopus 로고    scopus 로고
    • Takeda Pharmaceutical Co. Ltd. WO2012018058; 2012
    • Takeda Pharmaceutical Co. Ltd. WO2012018058; 2012
  • 64
    • 84871527975 scopus 로고    scopus 로고
    • Takeda Pharmaceutical Co. Ltd. WO2012020780; 2012
    • Takeda Pharmaceutical Co. Ltd. WO2012020780; 2012
  • 65
    • 84871529575 scopus 로고    scopus 로고
    • Takeda Pharmaceutical Co. Ltd. WO2011163355; 2011
    • Takeda Pharmaceutical Co. Ltd. WO2011163355; 2011
  • 66
    • 84871515722 scopus 로고    scopus 로고
    • Takeda Pharmaceutical Co. Ltd. WO2012018909; 2012
    • Takeda Pharmaceutical Co. Ltd. WO2012018909; 2012
  • 67
    • 84871498735 scopus 로고    scopus 로고
    • Janssen Pharmaceutica NV BELG. WO2011051342; 2011
    • Janssen Pharmaceutica NV, BELG. WO2011051342; 2011
  • 68
    • 84871507049 scopus 로고    scopus 로고
    • Janssen Pharmaceutica NV BELG. WO2011110545; 2011
    • Janssen Pharmaceutica NV, BELG. WO2011110545; 2011
  • 69
    • 84871499037 scopus 로고    scopus 로고
    • Sunovion Pharmaceuticals, Inc. WO2011150156; 2011
    • Sunovion Pharmaceuticals, Inc. WO2011150156; 2011
  • 70
    • 84871526984 scopus 로고    scopus 로고
    • Sunovion Pharmaceuticals, Inc. US20120178748; 2012
    • Sunovion Pharmaceuticals, Inc. US20120178748; 2012
  • 71
    • 84871518876 scopus 로고    scopus 로고
    • Mitsubishi Tanabe Pharma Corp. WO2010027097; 2010
    • Mitsubishi Tanabe Pharma Corp. WO2010027097; 2010
  • 72
    • 84871495189 scopus 로고    scopus 로고
    • Mitsubishi Tanabe Pharma Corp. WO2010030027; 2010
    • Mitsubishi Tanabe Pharma Corp. WO2010030027; 2010
  • 73
    • 84871502962 scopus 로고    scopus 로고
    • Mitsubishi Tanabe Pharma Corp. WO2011105628; 2011
    • Mitsubishi Tanabe Pharma Corp. WO2011105628; 2011
  • 74
    • 68349137530 scopus 로고    scopus 로고
    • Cross-linking of protein crystals as an aid in the generation of binary protein-ligand crystal complexes, exemplified by the human PDE10a-papaverine structure
    • Andersen OA, Schoenfeld DL, Toogood-Johnson I, et al. Cross-linking of protein crystals as an aid in the generation of binary protein-ligand crystal complexes, exemplified by the human PDE10a-papaverine structure. Acta Crystallogr D Biol Crystallogr 2009;D65(8):872-4
    • (2009) Acta Crystallogr D Biol Crystallogr , vol.65 , Issue.8 , pp. 872-874
    • Andersen, O.A.1    Schoenfeld, D.L.2    Toogood-Johnson, I.3
  • 75
    • 67650951150 scopus 로고    scopus 로고
    • The multiple roles of computational chemistry in fragment-based drug design
    • Law R, Barker O, Barker JJ, et al. The multiple roles of computational chemistry in fragment-based drug design. J Comput Aided Mol Des 2009;23:459-73
    • (2009) J Comput Aided Mol des , vol.23 , pp. 459-473
    • Law, R.1    Barker, O.2    Barker, J.J.3
  • 76
    • 84871499679 scopus 로고    scopus 로고
    • Evotec (UK) Ltd. WO2012019954; 2012
    • Evotec (UK) Ltd. WO2012019954; 2012
  • 77
    • 84871499054 scopus 로고    scopus 로고
    • Amgen, Inc. WO2010057126; 2010
    • Amgen, Inc. WO2010057126; 2010
  • 78
    • 84871494713 scopus 로고    scopus 로고
    • Amgen, Inc. WO2010057121; 2010
    • Amgen, Inc. WO2010057121; 2010
  • 79
    • 84871501616 scopus 로고    scopus 로고
    • Amgen, Inc. US20100160280; 2010
    • Amgen, Inc. US20100160280; 2010
  • 80
    • 84871503488 scopus 로고    scopus 로고
    • Amgen, Inc. WO2011143365; 2011
    • Amgen, Inc. WO2011143365; 2011
  • 81
    • 84871491355 scopus 로고    scopus 로고
    • Amgen, Inc. WO2011143366; 2011
    • Amgen, Inc. WO2011143366; 2011
  • 82
    • 84871478321 scopus 로고    scopus 로고
    • Amgen, Inc. WO2011143495; 2011
    • Amgen, Inc. WO2011143495; 2011
  • 83
    • 84871529650 scopus 로고    scopus 로고
    • Amgen, Inc. WO2011143129; 2011
    • Amgen, Inc. WO2011143129; 2011
  • 84
    • 84871514295 scopus 로고    scopus 로고
    • Janssen Pharmaceutica NV. WO2010097367; 2010
    • Janssen Pharmaceutica NV. WO2010097367; 2010
  • 85
    • 84871522799 scopus 로고    scopus 로고
    • Janssen Pharmaceutica NV. WO2011051324; 2011
    • Janssen Pharmaceutica NV. WO2011051324; 2011
  • 86
    • 79851490485 scopus 로고    scopus 로고
    • Preclinical evaluation of 18F-JNJ41510417 as a radioligand for PET imaging of phosphodiesterase-10A in the brain
    • Celen S, Koole M, De AM, et al. Preclinical evaluation of 18F-JNJ41510417 as a radioligand for PET imaging of phosphodiesterase-10A in the brain. J Nucl Med 2010;51:1584-91
    • (2010) J Nucl Med , vol.51 , pp. 1584-1591
    • Celen, S.1    Koole, M.2    De, A.M.3
  • 87
    • 80051897157 scopus 로고    scopus 로고
    • Synthesis, in vivo occupancy, and radiolabeling of potent phosphodiesterase subtype-10inhibitors as candidates for positron emission tomography imaging
    • Andres J-I, Angelis MD, Alcazar J, et al. Synthesis, in vivo occupancy, and radiolabeling of potent phosphodiesterase subtype-10inhibitors as candidates for positron emission tomography imaging. J Med Chem 2011;54:5820-35
    • (2011) J Med Chem , vol.54 , pp. 5820-5835
    • Andres, J.-I.1    Angelis, M.D.2    Alcazar, J.3
  • 88
    • 84871522196 scopus 로고    scopus 로고
    • Merck Sharp & Dohme Corp. WO2010138577; 2010
    • Merck Sharp & Dohme Corp. WO2010138577; 2010
  • 89
    • 84871504241 scopus 로고    scopus 로고
    • H. Lundbeck A/S. WO2012062319; 2012
    • H. Lundbeck A/S. WO2012062319; 2012
  • 90
    • 77952551015 scopus 로고    scopus 로고
    • Carbon-11 labeled papaverine as a pet tracer for imaging pde10a: Radiosyn thesis in vitro and in vivo evaluation
    • Tu Z, Xu J, Jones LA, et al. Carbon-11 labeled papaverine as a PET tracer for imaging PDE10A: radiosynthesis, in vitro and in vivo evaluation. Nucl Med Biol 2010;37:509-16
    • (2010) Nucl Med Biol , vol.37 , pp. 509-516
    • Tu, Z.1    Xu, J.2    Jones, L.A.3
  • 91
    • 79952186381 scopus 로고    scopus 로고
    • Radiosynthesis and in vivo evaluation of [11C] MP-10 as a PET probe for imaging PDE10A in rodent and non-human primate brain
    • Tu Z, Fan J, Li S, et al. Radiosynthesis and in vivo evaluation of [11C]MP-10 as a PET probe for imaging PDE10A in rodent and non-human primate brain. Bioorg Med Chem 2011;19:1666-73
    • (2011) Bioorg Med Chem , vol.19 , pp. 1666-1673
    • Tu, Z.1    Fan, J.2    Li, S.3
  • 92
    • 84857677917 scopus 로고    scopus 로고
    • Radiosynthesis and radiotracer properties of a 7-(2-[18f] fluoroethoxy)-6- methoxypyrrolidinylquinazoline for imaging of phosphodiesterase 10a with pet
    • Funke U, Deuther-Conrad W, Schwan G, et al. Radiosynthesis and radiotracer properties of a 7-(2-[18F] Fluoroethoxy)-6- methoxypyrrolidinylquinazoline for imaging of phosphodiesterase 10A with PET. Pharmaceuticals 2012;5:169-88
    • (2012) Pharmaceuticals , vol.5 , pp. 169-188
    • Funke, U.1    Deuther-Conrad, W.2    Schwan, G.3
  • 93
    • 84861491053 scopus 로고    scopus 로고
    • Rapid identification of a novel small molecule phosphodiesterase 10A (PDE10A) tracer
    • Hu E, Ma J, Biorn C, et al. Rapid identification of a novel small molecule phosphodiesterase 10A (PDE10A) tracer. J Med Chem 2012;5:4776-87
    • (2012) J Med Chem , Issue.5 , pp. 4776-4787
    • Hu, E.1    Ma, J.2    Biorn, C.3
  • 94
    • 84857355907 scopus 로고    scopus 로고
    • Discovery of 4-hydroxy-1, 6-naphthyridine-3-carbonitrile derivatives as novel PDE10A inhibitors
    • AstraZeneca. Bauer U, Giordanetto F, Bauer M. Discovery of 4-hydroxy-1, 6-naphthyridine-3-carbonitrile derivatives as novel PDE10A inhibitors. Bioorg Med Chem Lett 2012;22:1944-8
    • (2012) Bioorg Med Chem Lett , pp. 22
    • Astrazeneca, B.U.1    Giordanetto, F.2    Bauer, M.3


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