메뉴 건너뛰기




Volumn 18, Issue 10, 2008, Pages 1127-1139

PDE7 inhibitors as new drugs for neurological and inflammatory disorders

Author keywords

Dual PDE7 PDE4 inhibitors; Inflammatory diseases; Neurological diseases; PDE7 inhibitors

Indexed keywords

2 [4 [6,7 DIETHOXY 2,3 BIS(HYDROXYMETHYL) 1 NAPHTHYL] 2 PYRIDYL] 4 (3 PYRIDYL) 1(2H) PHTHALAZINONE; 2 METHYL 5 NITROBENZENESULFONIC ACID DIMETHYLAMIDE; AZO COMPOUND; HETEROCYCLIC COMPOUND; PHOSPHODIESTERASE INHIBITOR; PHOSPHODIESTERASE IV INHIBITOR; PHOSPHODIESTERASE VII INHIBITOR; PHTALAZINONE DERIVATIVE; PURINE ANTAGONIST; PYRIMIDINE ANTAGONIST; SPIROQUINOZOLINONE DERIVATIVE; UNCLASSIFIED DRUG; YM 393059;

EID: 56349091430     PISSN: 13543776     EISSN: None     Source Type: Journal    
DOI: 10.1517/13543776.18.10.1127     Document Type: Review
Times cited : (43)

References (82)
  • 1
    • 31144433061 scopus 로고    scopus 로고
    • Cyclic nucleotide phosphodiesterase (PDE) superfamily: A new target for the development of specific therapeutic agents
    • Lugnier C. Cyclic nucleotide phosphodiesterase (PDE) superfamily: a new target for the development of specific therapeutic agents. Pharmacol Ther 2006;109:366-98
    • (2006) Pharmacol Ther , vol.109 , pp. 366-398
    • Lugnier, C.1
  • 2
    • 0029062054 scopus 로고
    • Theophylline and selective phosphodiesterase inhibitors as anti-inflammatory drugs in the treatment of bronchial asthma
    • Banner KH, Page CP. Theophylline and selective phosphodiesterase inhibitors as anti-inflammatory drugs in the treatment of bronchial asthma. Eur Respir J 1995;8:996-1000
    • (1995) Eur Respir J , vol.8 , pp. 996-1000
    • Banner, K.H.1    Page, C.P.2
  • 3
    • 0032899660 scopus 로고    scopus 로고
    • Cyclic nucleotide phosphodiesterase (PDE) inhibitors and immunomo-dulation
    • Essayan DM. Cyclic nucleotide phosphodiesterase (PDE) inhibitors and immunomo-dulation. Biochem Pharmacol 1999;57:965-73
    • (1999) Biochem Pharmacol , vol.57 , pp. 965-973
    • Essayan, D.M.1
  • 4
    • 36749058569 scopus 로고    scopus 로고
    • Cilostazol: A new drug in die treatment intermittent claudication
    • Kumar M, Bhattacharya. V. Cilostazol: a new drug in die treatment intermittent claudication. Recent Patents Cardiovasc Drug Discov 2007;2:181-5
    • (2007) Recent Patents Cardiovasc Drug Discov , vol.2 , pp. 181-185
    • Kumar, M.1    Bhattacharya, V.2
  • 6
    • 38449113123 scopus 로고    scopus 로고
    • Hatzimouratidis K. Sildenafil in the treatment of erectile dysfunction: an overview of the clinical evidence. Clin Interv Aging 2006;1:403-14
    • Hatzimouratidis K. Sildenafil in the treatment of erectile dysfunction: an overview of the clinical evidence. Clin Interv Aging 2006;1:403-14
  • 7
    • 33746629480 scopus 로고    scopus 로고
    • Menniti FS, Faraci WS, Schmidt CJ. Phosphodiesterases in the CNS: targets for drug development. Nat Rev Drug Discov 2006;5:660-70
    • Menniti FS, Faraci WS, Schmidt CJ. Phosphodiesterases in the CNS: targets for drug development. Nat Rev Drug Discov 2006;5:660-70
  • 8
    • 35948933492 scopus 로고    scopus 로고
    • Potential CNS applications for PDEs inhibitors
    • Brandon NJ, Rotella DP. Potential CNS applications for PDEs inhibitors. Ann Rep Med Chem 2007;42:3-12
    • (2007) Ann Rep Med Chem , vol.42 , pp. 3-12
    • Brandon, N.J.1    Rotella, D.P.2
  • 9
    • 35148895860 scopus 로고    scopus 로고
    • PDE inhibitors in psychiatry-future options for dementia, depression and schizophrenia?
    • Halene TB, Siegel SJ. PDE inhibitors in psychiatry-future options for dementia, depression and schizophrenia? Drug Discov Today 2007;12:870-8
    • (2007) Drug Discov Today , vol.12 , pp. 870-878
    • Halene, T.B.1    Siegel, S.J.2
  • 10
    • 24944520099 scopus 로고    scopus 로고
    • Phosphodiesterase inhibitors for cognitive enhancement
    • Rose GM, Hopper A, De Vivo M, Tehim A. Phosphodiesterase inhibitors for cognitive enhancement. Curr Pharm Des 2005;11:3329-33
    • (2005) Curr Pharm Des , vol.11 , pp. 3329-3333
    • Rose, G.M.1    Hopper, A.2    De Vivo, M.3    Tehim, A.4
  • 11
    • 33846376947 scopus 로고    scopus 로고
    • Cilostazol, a phosphodiesterase 3 inhibitor, protects mice against acute and late ischemic brain injuries
    • Ye YL, Shi WZ, Zhang WP, et al. Cilostazol, a phosphodiesterase 3 inhibitor, protects mice against acute and late ischemic brain injuries. Eur J Pharmacol 2007;557:23-31
    • (2007) Eur J Pharmacol , vol.557 , pp. 23-31
    • Ye, Y.L.1    Shi, W.Z.2    Zhang, W.P.3
  • 12
    • 41949137657 scopus 로고    scopus 로고
    • Cilostazol promotes survival of axotomized retinal ganglion cells in adult rats
    • Kashimoto R, Kurimoto T, Miyoshi T, et al. Cilostazol promotes survival of axotomized retinal ganglion cells in adult rats. Neurosci Lett 2008;436:116-19
    • (2008) Neurosci Lett , vol.436 , pp. 116-119
    • Kashimoto, R.1    Kurimoto, T.2    Miyoshi, T.3
  • 13
    • 34247368526 scopus 로고    scopus 로고
    • Sildenafil citrate attenuates a complex maze impairment induced by intracerebroventricular infusion of the NOS inhibitor N Ω-nitro-L-arginine methyl ester
    • Devan BD, Pistell PJ, Daffin LW Jr, et al. Sildenafil citrate attenuates a complex maze impairment induced by intracerebroventricular infusion of the NOS inhibitor N Ω-nitro-L-arginine methyl ester. Eur J Pharmacol 2007;563:134-40
    • (2007) Eur J Pharmacol , vol.563 , pp. 134-140
    • Devan, B.D.1    Pistell, P.J.2    Daffin Jr, L.W.3
  • 14
    • 42449099422 scopus 로고    scopus 로고
    • Preclinical characterization of selective phosphodiesterase 10A inhibitors: A new therapeutic approach to the treatment of schizophrenia
    • Schmidt CJ, Chapin DS, Cianfrogna J, et al. Preclinical characterization of selective phosphodiesterase 10A inhibitors: a new therapeutic approach to the treatment of schizophrenia. J Pharmacol Exp Ther 2008;325:681-90
    • (2008) J Pharmacol Exp Ther , vol.325 , pp. 681-690
    • Schmidt, C.J.1    Chapin, D.S.2    Cianfrogna, J.3
  • 15
    • 33645229167 scopus 로고    scopus 로고
    • Selective phosphodiesterase (PDE)-4 inhibitors: A novel approach to treating memory deficit?
    • Ghavami A, Hirst WD, Novak TJ. Selective phosphodiesterase (PDE)-4 inhibitors: a novel approach to treating memory deficit? Drugs R D 2006;7:63-71
    • (2006) Drugs R D , vol.7 , pp. 63-71
    • Ghavami, A.1    Hirst, W.D.2    Novak, T.J.3
  • 16
    • 56349100011 scopus 로고    scopus 로고
    • Available from
    • Available from: http://www.memorypharma.com/p_MEM1414.html
  • 17
    • 0041695221 scopus 로고    scopus 로고
    • Alterations on phosphodiesterase type 7 and 8 isozyme mRNA expression in Alzheimer's disease brains examined by in situ hybridization
    • Pérez-Torres S, Cortés R, Tolnay M, et al. Alterations on phosphodiesterase type 7 and 8 isozyme mRNA expression in Alzheimer's disease brains examined by in situ hybridization. Exp Neurol 2003;182:322-34
    • (2003) Exp Neurol , vol.182 , pp. 322-334
    • Pérez-Torres, S.1    Cortés, R.2    Tolnay, M.3
  • 18
    • 0033524977 scopus 로고    scopus 로고
    • CD3- and CD28-dependent induction of PDE7 required for T cell activation
    • Li L, Yee C, Beavo JA. CD3- and CD28-dependent induction of PDE7 required for T cell activation. Science 1999;283:848-51
    • (1999) Science , vol.283 , pp. 848-851
    • Li, L.1    Yee, C.2    Beavo, J.A.3
  • 19
    • 33748529283 scopus 로고    scopus 로고
    • Phosphodiesterase 7A: A new therapeutic target for alleviating chronic inflammation?
    • Giembycz MA, Smith SJ. Phosphodiesterase 7A: a new therapeutic target for alleviating chronic inflammation? Curr Pharm. Des 2006;12:3207-20
    • (2006) Curr Pharm. Des , vol.12 , pp. 3207-3220
    • Giembycz, M.A.1    Smith, S.J.2
  • 20
    • 33646798806 scopus 로고    scopus 로고
    • Phosphodiesterase 7 (PDE7) as a therapeutic target
    • Giembycz MA, Smith SJ. Phosphodiesterase 7 (PDE7) as a therapeutic target. Drugs Fut 2006;31:207-29
    • (2006) Drugs Fut , vol.31 , pp. 207-229
    • Giembycz, M.A.1    Smith, S.J.2
  • 21
    • 0037308172 scopus 로고    scopus 로고
    • Ubiquitous expression of phosphodiesterase 7A in human proinflammatory and immune cells
    • Smith SJ, Brookes-Fazakerley S, et al. Ubiquitous expression of phosphodiesterase 7A in human proinflammatory and immune cells. Am J Physiol Lung Cell Mol Physiol 2003;284:L279-89
    • (2003) Am J Physiol Lung Cell Mol Physiol , vol.284
    • Smith, S.J.1    Brookes-Fazakerley, S.2
  • 22
    • 0034720463 scopus 로고    scopus 로고
    • Cloning and characterization of the human and mouse PDE7B, a novel cAMP-specific cyclic nucleotide phosphodiesterase
    • Gardner C, Robas N, Cawkill D, Fidock M. Cloning and characterization of the human and mouse PDE7B, a novel cAMP-specific cyclic nucleotide phosphodiesterase. Biochem Biophys Res Commun 2000;272:186-92
    • (2000) Biochem Biophys Res Commun , vol.272 , pp. 186-192
    • Gardner, C.1    Robas, N.2    Cawkill, D.3    Fidock, M.4
  • 23
    • 0035372036 scopus 로고    scopus 로고
    • Differential distribution of cAMP-specific phosphodiesterase 7A mRNA in rat brain and peripheral organs
    • Miró X, Pérez-Torres S, Palacios JM, et al. Differential distribution of cAMP-specific phosphodiesterase 7A mRNA in rat brain and peripheral organs. Synapse 2001;40:201-14
    • (2001) Synapse , vol.40 , pp. 201-214
    • Miró, X.1    Pérez-Torres, S.2    Palacios, J.M.3
  • 24
    • 18044376227 scopus 로고    scopus 로고
    • Neuronal expression of cAMP-specific phosphodiesterase 7B mRNA in the rat brain
    • Reyes-Irisarri E, Pérez-Torres S, Mengod G. Neuronal expression of cAMP-specific phosphodiesterase 7B mRNA in the rat brain. Neuroscience 2005;132:1173-85
    • (2005) Neuroscience , vol.132 , pp. 1173-1185
    • Reyes-Irisarri, E.1    Pérez-Torres, S.2    Mengod, G.3
  • 25
    • 0346996880 scopus 로고    scopus 로고
    • Phosphodiesterase 7A-deficient mice have functional T cells
    • Yang G, McIntyre KW, Townsend RM, et al. Phosphodiesterase 7A-deficient mice have functional T cells. J Immunol 2003;171:6414-20
    • (2003) J Immunol , vol.171 , pp. 6414-6420
    • Yang, G.1    McIntyre, K.W.2    Townsend, R.M.3
  • 26
    • 0036277784 scopus 로고    scopus 로고
    • Potential role of phosphodiesterase 7 in human T cell function: Comparative effects of two phosphodiesterase inhibitors
    • Nakata A, Ogawa K. Sasaki T, et al. Potential role of phosphodiesterase 7 in human T cell function: comparative effects of two phosphodiesterase inhibitors. Clin Exp Immunol 2002;128:460-6
    • (2002) Clin Exp Immunol , vol.128 , pp. 460-466
    • Nakata, A.1    Ogawa, K.2    Sasaki, T.3
  • 27
    • 33646454098 scopus 로고    scopus 로고
    • PDE7 inhibitors: Chemistry and potential therapeutic utilities
    • Vergne F, Bernardelli P, Chevalier E. PDE7 inhibitors: chemistry and potential therapeutic utilities. Ann Rep Med Chem 2005;40:227-41
    • (2005) Ann Rep Med Chem , vol.40 , pp. 227-241
    • Vergne, F.1    Bernardelli, P.2    Chevalier, E.3
  • 28
    • 37249092594 scopus 로고    scopus 로고
    • Cloning, stable expression of human phosphodiesterase 7A and development of an assay for screening of PDE7 selective inhibitors
    • Malik R, Bora RS, Gupta D, et al. Cloning, stable expression of human phosphodiesterase 7A and development of an assay for screening of PDE7 selective inhibitors. Appl Microbiol Biotechnol 2008;77:1167-73
    • (2008) Appl Microbiol Biotechnol , vol.77 , pp. 1167-1173
    • Malik, R.1    Bora, R.S.2    Gupta, D.3
  • 29
    • 33847689816 scopus 로고    scopus 로고
    • Crystal structures of phosphodiesterases and implications on substrate specificity and inhibitor selectivity
    • Ke H, Wang H. Crystal structures of phosphodiesterases and implications on substrate specificity and inhibitor selectivity. Curr Top Med Chem 2007;7:391-403
    • (2007) Curr Top Med Chem , vol.7 , pp. 391-403
    • Ke, H.1    Wang, H.2
  • 30
    • 0343986277 scopus 로고    scopus 로고
    • Benzyl derivatives of 2,1,3-benzo- and benzothieno[3,2-a]thiadiazine 2,2-dioxides: First phosphodiesterase 7 inhibitors
    • Martínez A. Castro A, Gil C, et al. Benzyl derivatives of 2,1,3-benzo- and benzothieno[3,2-a]thiadiazine 2,2-dioxides: first phosphodiesterase 7 inhibitors. J Med Chem 2000;43:683-9
    • (2000) J Med Chem , vol.43 , pp. 683-689
    • Martínez, A.1    Castro, A.2    Gil, C.3
  • 31
    • 14544272401 scopus 로고    scopus 로고
    • Cyclic nucleotide phosphodiesterases and their role in immunomodulatory responses: Advances in the development of specific phosphodiesterase inhibitors
    • Castro A, Jerez MJ, Gil C, Martinez A. Cyclic nucleotide phosphodiesterases and their role in immunomodulatory responses: advances in the development of specific phosphodiesterase inhibitors. Med Res Rev 2005;25:229-44
    • (2005) Med Res Rev , vol.25 , pp. 229-244
    • Castro, A.1    Jerez, M.J.2    Gil, C.3    Martinez, A.4
  • 32
    • 0036151438 scopus 로고    scopus 로고
    • PDE7A is expressed in human B-lymphocytes and is up-regulated by elevation of intracellular cAMP
    • Lee R, Wolda S, Moon E, et al. PDE7A is expressed in human B-lymphocytes and is up-regulated by elevation of intracellular cAMP. Cell Signal 2002;14:277-84
    • (2002) Cell Signal , vol.14 , pp. 277-284
    • Lee, R.1    Wolda, S.2    Moon, E.3
  • 33
    • 9444228283 scopus 로고    scopus 로고
    • Discovery of BRL 50481 [3-(N,N-dimethylsulfonamido)-4-methylnitrobenzene], a selective inhibitor of phosphodiesterase 7: In vitro studies in human monocytes, lung macrophages, and CD8+T-lymphocytes
    • Smith SJ, Cieslinski LB, Newton R, et al. Discovery of BRL 50481 [3-(N,N-dimethylsulfonamido)-4-methylnitrobenzene], a selective inhibitor of phosphodiesterase 7: in vitro studies in human monocytes, lung macrophages, and CD8+T-lymphocytes. Mol Pharmacol 2004;66:1679-89
    • (2004) Mol Pharmacol , vol.66 , pp. 1679-1689
    • Smith, S.J.1    Cieslinski, L.B.2    Newton, R.3
  • 34
    • 18744393466 scopus 로고    scopus 로고
    • Life after PDE4: Overcoming adverse events with dual-specificity phosphodiesterase inhibitors
    • Giembycz MA. Life after PDE4: overcoming adverse events with dual-specificity phosphodiesterase inhibitors. Curr Opin Pharmacol 2005;5:238-44
    • (2005) Curr Opin Pharmacol , vol.5 , pp. 238-244
    • Giembycz, M.A.1
  • 35
    • 33847109728 scopus 로고    scopus 로고
    • Amelioration of collagen-induced arthritis in mice by a novel phosphodiesterase 7 and 4 dual inhibitor, YM-393059
    • Yamamoto S, Sugahara S, Ikeda K, Shimizu Y. Amelioration of collagen-induced arthritis in mice by a novel phosphodiesterase 7 and 4 dual inhibitor, YM-393059. Eur J Pharmacol 2007;559:219-26
    • (2007) Eur J Pharmacol , vol.559 , pp. 219-226
    • Yamamoto, S.1    Sugahara, S.2    Ikeda, K.3    Shimizu, Y.4
  • 36
    • 2342516888 scopus 로고    scopus 로고
    • Identification of purine inhibitors of phosphodiesterase 7 (PDE7)
    • Pitts WJ, Vaccaro W, Huynh T, et al. Identification of purine inhibitors of phosphodiesterase 7 (PDE7). Bioorg Med Chem Lett 2004;14:2955-8
    • (2004) Bioorg Med Chem Lett , vol.14 , pp. 2955-2958
    • Pitts, W.J.1    Vaccaro, W.2    Huynh, T.3
  • 37
    • 20144366973 scopus 로고    scopus 로고
    • Fused pyrimidine based inhibitors of phosphodiesterase 7 (PDE7): Synthesis and initial structure-activity relationships
    • Kempson J, Pitts WJ, Barbosa J, et al. Fused pyrimidine based inhibitors of phosphodiesterase 7 (PDE7): synthesis and initial structure-activity relationships. Bioorg Med Chem Lett 2005;15:1829-33
    • (2005) Bioorg Med Chem Lett , vol.15 , pp. 1829-1833
    • Kempson, J.1    Pitts, W.J.2    Barbosa, J.3
  • 38
    • 0035938422 scopus 로고    scopus 로고
    • Synthesis and structure-activity relationships of guanine analogues as phosphodiesterase 7 (PDE7) inhibitors
    • Barnes MJ, Cooper N, Davenport RJ, et al. Synthesis and structure-activity relationships of guanine analogues as phosphodiesterase 7 (PDE7) inhibitors. Bioorg Med Chem Lett 2001;11:1081-3
    • (2001) Bioorg Med Chem Lett , vol.11 , pp. 1081-1083
    • Barnes, M.J.1    Cooper, N.2    Davenport, R.J.3
  • 39
    • 56349155496 scopus 로고    scopus 로고
    • Darwin Discovery Limited. 9-(1,2,3,4-Tetrahydronaphthalen-1-yl)-1,9-dihydropurin-6-one derivatives as PDE7 inhibitors. WO0068230; 2000
    • Darwin Discovery Limited. 9-(1,2,3,4-Tetrahydronaphthalen-1-yl)-1,9-dihydropurin-6-one derivatives as PDE7 inhibitors. WO0068230; 2000
  • 40
    • 56349167431 scopus 로고    scopus 로고
    • Bristol-Myers Squibb. Fused heterocyclic inhibitors of phosphodiesterase (PDE) 7. WO02087513; 2002
    • Bristol-Myers Squibb. Fused heterocyclic inhibitors of phosphodiesterase (PDE) 7. WO02087513; 2002
  • 41
    • 56349117077 scopus 로고    scopus 로고
    • Bristol-Myers Squibb. Purine inhibitors of phosphodiesterase (PDE) 7. WO02102314; 2002
    • Bristol-Myers Squibb. Purine inhibitors of phosphodiesterase (PDE) 7. WO02102314; 2002
  • 42
    • 56349168795 scopus 로고    scopus 로고
    • Bristol-Myers Squibb. Pyrimidine inhibitors of phosphodiesterase (PDE) 7. WO02102313; 2002
    • Bristol-Myers Squibb. Pyrimidine inhibitors of phosphodiesterase (PDE) 7. WO02102313; 2002
  • 43
    • 56349083117 scopus 로고    scopus 로고
    • Pharma. 1,3,5-Trisubstituted-5-phenyl and 5-pyridyl pyrazolopyrimidinone derivatives having PDE7 inhibiting action
    • US007268128;
    • Ausbio Pharma. 1,3,5-Trisubstituted-5-phenyl and 5-pyridyl pyrazolopyrimidinone derivatives having PDE7 inhibiting action. US007268128; 2007
    • (2007)
    • Ausbio1
  • 44
    • 56349143153 scopus 로고    scopus 로고
    • Bristol-Myers Squibb. Quinazoline and pyrido[2,3-D]pyrimidine inhibitors of phosphodiesterase (PDE) 7. US007022849B2; 2006
    • Bristol-Myers Squibb. Quinazoline and pyrido[2,3-D]pyrimidine inhibitors of phosphodiesterase (PDE) 7. US007022849B2; 2006
  • 45
    • 56349141875 scopus 로고    scopus 로고
    • Bristol-Myers Squibb. Quinazoline and pyrido[2,3-D]pyrimidine inhibitors of phosphodiesterase (PDE) 7. US20060116516A1; 2006
    • Bristol-Myers Squibb. Quinazoline and pyrido[2,3-D]pyrimidine inhibitors of phosphodiesterase (PDE) 7. US20060116516A1; 2006
  • 46
    • 56349154791 scopus 로고    scopus 로고
    • Celltech Chiroscience Ltd. Heterobiarylsulphonamides and their use as PDE7 inhibitors. WO0174786; 2001
    • Celltech Chiroscience Ltd. Heterobiarylsulphonamides and their use as PDE7 inhibitors. WO0174786; 2001
  • 47
    • 56349140476 scopus 로고    scopus 로고
    • Celltech Chiroscience Ltd. Sulphonamide derivatives. WO0198274; 2001
    • Celltech Chiroscience Ltd. Sulphonamide derivatives. WO0198274; 2001
  • 48
    • 56349120994 scopus 로고    scopus 로고
    • Compounds and their use as PDE inhibitors
    • US0020156064;
    • Smithkline Beecham Corp. Compounds and their use as PDE inhibitors. US0020156064; 2002
    • (2002)
    • Beecham Corp, S.1
  • 49
    • 56349125974 scopus 로고    scopus 로고
    • BYK Gulden Lomberg Chemische Fabrik GMBH. Dihydroisoquinolines as novel phosphodiesterase inhibitors. WO0240449; 2002
    • BYK Gulden Lomberg Chemische Fabrik GMBH. Dihydroisoquinolines as novel phosphodiesterase inhibitors. WO0240449; 2002
  • 50
    • 56349111317 scopus 로고    scopus 로고
    • BYK Gulden Lomberg; Chemische Fabrik GMBH. (Dihydro)isoquinolines derivatives as phosphodiesterase inhibitors. WO0240450; 2002
    • BYK Gulden Lomberg; Chemische Fabrik GMBH. (Dihydro)isoquinolines derivatives as phosphodiesterase inhibitors. WO0240450; 2002
  • 51
    • 44949224387 scopus 로고    scopus 로고
    • Effects of phosphodiesterase 7 inhibition by RNA interference on the gene expression and differentiation of human mesenchymal stem cell-derived osteoblasts
    • Pekkinen M, Ahlström MEB, Riehle U, et al. Effects of phosphodiesterase 7 inhibition by RNA interference on the gene expression and differentiation of human mesenchymal stem cell-derived osteoblasts. Bone 2008;43:84-91
    • (2008) Bone , vol.43 , pp. 84-91
    • Pekkinen, M.1    Ahlström, M.E.B.2    Riehle, U.3
  • 52
    • 47549093542 scopus 로고    scopus 로고
    • Stereoelectronic properties of spiroquinazolinones in differential PDE7 inhibitory activity
    • Daga PR, Doerksen RJ. Stereoelectronic properties of spiroquinazolinones in differential PDE7 inhibitory activity. J Comput Chem 2008;29:1945-54
    • (2008) J Comput Chem , vol.29 , pp. 1945-1954
    • Daga, P.R.1    Doerksen, R.J.2
  • 53
    • 8544276586 scopus 로고    scopus 로고
    • Spiroquinazolinones as novel, potent, and selective PDE7 inhibitors. Part 1
    • Lorthiois E, Bernardelli P, Vergne F, et al. Spiroquinazolinones as novel, potent, and selective PDE7 inhibitors. Part 1. Bioorg Med Chem Lett 2004;14:4623-6
    • (2004) Bioorg Med Chem Lett , vol.14 , pp. 4623-4626
    • Lorthiois, E.1    Bernardelli, P.2    Vergne, F.3
  • 54
    • 8544260347 scopus 로고    scopus 로고
    • Spiroquinazolinones as novel, potent, and selective PDE7 inhibitors. Part 2: Optimization of 5,8-disubstituted derivatives
    • Bernardelli P, Lorthiois E, Vergne F, et al. Spiroquinazolinones as novel, potent, and selective PDE7 inhibitors. Part 2: Optimization of 5,8-disubstituted derivatives. Bioorg Med Chem Lett 2004;14:4627-31
    • (2004) Bioorg Med Chem Lett , vol.14 , pp. 4627-4631
    • Bernardelli, P.1    Lorthiois, E.2    Vergne, F.3
  • 55
    • 56349108413 scopus 로고    scopus 로고
    • Pfizer Ltd. Spirocyclic derivatives. WO2007063391; 2007
    • Pfizer Ltd. Spirocyclic derivatives. WO2007063391; 2007
  • 56
    • 56349126739 scopus 로고    scopus 로고
    • Warner-Lambert. New spirocondensed quinazolinones and their use as phosphodiesterase inhibitors. WO2004/026818; 2004
    • Warner-Lambert. New spirocondensed quinazolinones and their use as phosphodiesterase inhibitors. WO2004/026818; 2004
  • 57
    • 56349095062 scopus 로고    scopus 로고
    • Warner-Lambert. New spirotricyclic derivatives and their use as phosphodiesterase-7 inhibitors. WO02/076953A1; 2002
    • Warner-Lambert. New spirotricyclic derivatives and their use as phosphodiesterase-7 inhibitors. WO02/076953A1; 2002
  • 58
    • 56349160442 scopus 로고    scopus 로고
    • Warner-Lambert. New spirotricyclic derivatives and their use as phosphodiesterase-7 inhibitors. WO02074754; 2002
    • Warner-Lambert. New spirotricyclic derivatives and their use as phosphodiesterase-7 inhibitors. WO02074754; 2002
  • 59
    • 56349111741 scopus 로고    scopus 로고
    • Warner-Lambert. Spirotricyclic derivatives and their use as phosphodiesterase-7 inhibitors. US2002/0198198A1; 2002
    • Warner-Lambert. Spirotricyclic derivatives and their use as phosphodiesterase-7 inhibitors. US2002/0198198A1; 2002
  • 60
    • 56349140049 scopus 로고    scopus 로고
    • Pfizer Ltd. Use of PDE7 inhibitors for the treatment of neuropathic pain. WO2006092691; 2006
    • Pfizer Ltd. Use of PDE7 inhibitors for the treatment of neuropathic pain. WO2006092691; 2006
  • 61
    • 56349171100 scopus 로고    scopus 로고
    • Patent GMBH. Imidazole derivatives as phosphodiesterase VII inhibitors
    • WO0129049;
    • Merck Patent GMBH. Imidazole derivatives as phosphodiesterase VII inhibitors. WO0129049; 2001
    • (2001)
    • Merck1
  • 62
    • 56349171100 scopus 로고    scopus 로고
    • Patent GMBH. Isoxazole derivatives to be used as phosphodiesterase VII inhibitors
    • WO0132175;
    • Merck Patent GMBH. Isoxazole derivatives to be used as phosphodiesterase VII inhibitors. WO0132175; 2001
    • (2001)
    • Merck1
  • 63
    • 56349171100 scopus 로고    scopus 로고
    • Patent GMBH. Pyrrole derivatives as phosphodiesterase VII inhibitors
    • WO0132618;
    • Merck Patent GMBH. Pyrrole derivatives as phosphodiesterase VII inhibitors. WO0132618; 2001
    • (2001)
    • Merck1
  • 64
    • 56349171100 scopus 로고    scopus 로고
    • Patent GMBH. Imidazopyridine derivatives as phosphodiesterase VII inhibitors
    • WO0134601;
    • Merck Patent GMBH. Imidazopyridine derivatives as phosphodiesterase VII inhibitors. WO0134601; 2001
    • (2001)
    • Merck1
  • 65
    • 56349171100 scopus 로고    scopus 로고
    • Patent GMBH. Imidazole compounds used as phosphodiesterase VII inhibitors
    • WO0136425;
    • Merck Patent GMBH. Imidazole compounds used as phosphodiesterase VII inhibitors. WO0136425; 2001
    • (2001)
    • Merck1
  • 66
    • 8544250603 scopus 로고    scopus 로고
    • Discovery of thiadiazoles as a novel structural class of potent and selective PDE7 inhibitors. Part 1: Design, synthesis and structure-activity relationship studies
    • Vergne F, Bernardelli P. Lorthiois E, et al. Discovery of thiadiazoles as a novel structural class of potent and selective PDE7 inhibitors. Part 1: design, synthesis and structure-activity relationship studies. Bioorg Med Chem Lett 2004;14:4607-13
    • (2004) Bioorg Med Chem Lett , vol.14 , pp. 4607-4613
    • Vergne, F.1    Bernardelli, P.2    Lorthiois, E.3
  • 67
    • 8544256308 scopus 로고    scopus 로고
    • Discovery of thiadiazoles as a novel structural class of potent and selective PDE7 inhibitors. Part 2: Metabolism-directed optimization studies towards orally bioavailable derivatives
    • Vergne F, Bernardelli P, Lorthiois E, et al. Discovery of thiadiazoles as a novel structural class of potent and selective PDE7 inhibitors. Part 2: metabolism-directed optimization studies towards orally bioavailable derivatives. Bioorg Med Chem Lett 2004;14:4615-21
    • (2004) Bioorg Med Chem Lett , vol.14 , pp. 4615-4621
    • Vergne, F.1    Bernardelli, P.2    Lorthiois, E.3
  • 68
    • 33751043887 scopus 로고    scopus 로고
    • Phosphodiesterase (PDE) 7 in inflammatory cells from patients with asthma and COPD
    • Jones NA, Leport M, Holand T, et al. Phosphodiesterase (PDE) 7 in inflammatory cells from patients with asthma and COPD. Pulm. Pharmacol Ther 2007;20:60-8
    • (2007) Pulm. Pharmacol Ther , vol.20 , pp. 60-68
    • Jones, N.A.1    Leport, M.2    Holand, T.3
  • 69
    • 56349110736 scopus 로고    scopus 로고
    • Warner-Lambert. New thiadiazoles and their use as phosphodiesterase7-inhibitors. EP1193261A1; 2000
    • Warner-Lambert. New thiadiazoles and their use as phosphodiesterase7-inhibitors. EP1193261A1; 2000
  • 70
    • 56349135247 scopus 로고    scopus 로고
    • Warner-Lambert. (4,2-disubstituted-thiazol-5-yl)amine compounds as PDE7 inhibitors. WO03082839; 2003
    • Warner-Lambert. (4,2-disubstituted-thiazol-5-yl)amine compounds as PDE7 inhibitors. WO03082839; 2003
  • 71
    • 56349084479 scopus 로고    scopus 로고
    • Almirall Prodesfarma. 4-Aminothieno[2,3-d] pyrimidine-6-carbonitrile derivatives as PDE7 inhibitors. WO2004065391; 2004
    • Almirall Prodesfarma. 4-Aminothieno[2,3-d] pyrimidine-6-carbonitrile derivatives as PDE7 inhibitors. WO2004065391; 2004
  • 72
    • 35248887662 scopus 로고    scopus 로고
    • Small-molecule inhibitors of PDE-IV and - VII in the treatment of respiratory diseases and chronic inflammation
    • Vijayakrishnan L, Rudra S, Eapen MS, et al. Small-molecule inhibitors of PDE-IV and - VII in the treatment of respiratory diseases and chronic inflammation. Expert Opin Investig Drugs 2007;16:1585-99
    • (2007) Expert Opin Investig Drugs , vol.16 , pp. 1585-1599
    • Vijayakrishnan, L.1    Rudra, S.2    Eapen, M.S.3
  • 73
    • 0033602531 scopus 로고    scopus 로고
    • Novel, potent, and selective phosphodiesterase-4 inhibitors as antiasthmatic agents: Synthesis and biological activities of a series of 1-pyridylnaphthalene derivatives
    • Ukita T, Sugahara M, Terakawa Y, et al. Novel, potent, and selective phosphodiesterase-4 inhibitors as antiasthmatic agents: synthesis and biological activities of a series of 1-pyridylnaphthalene derivatives. J Med Chem 1999;42:1088-99
    • (1999) J Med Chem , vol.42 , pp. 1088-1099
    • Ukita, T.1    Sugahara, M.2    Terakawa, Y.3
  • 74
    • 33745137468 scopus 로고    scopus 로고
    • The effects of a novel phosphodiesterase 7A and -4 dual inhibitor, YM-393059, on T-cell-related cytokine production in vitro and in vivo
    • Yamamoto S, Sugahara. S, Naito R, et al. The effects of a novel phosphodiesterase 7A and -4 dual inhibitor, YM-393059, on T-cell-related cytokine production in vitro and in vivo. Eur J Pharmacol 2006;541:106-14
    • (2006) Eur J Pharmacol , vol.541 , pp. 106-114
    • Yamamoto, S.1    Sugahara, S.2    Naito, R.3
  • 75
    • 33749986292 scopus 로고    scopus 로고
    • Pharmacological profile of a novel phosphodiesterase inhibitor, YM-393059, on acute and chronic inflammation models
    • Yamamoto S, Sugahara S, Ikeda K, Shimizu, Y. Pharmacological profile of a novel phosphodiesterase inhibitor, YM-393059, on acute and chronic inflammation models. Eur J Pharmacol 2006;550:166-72
    • (2006) Eur J Pharmacol , vol.550 , pp. 166-172
    • Yamamoto, S.1    Sugahara, S.2    Ikeda, K.3    Shimizu, Y.4
  • 76
    • 56349093709 scopus 로고    scopus 로고
    • Bristol-Myers Squibb. Dual inhibitors of PDE7 and PDE4. WO02088079; 2002
    • Bristol-Myers Squibb. Dual inhibitors of PDE7 and PDE4. WO02088079; 2002
  • 77
    • 56349120526 scopus 로고    scopus 로고
    • Bristol-Myers Squibb. Dual inhibitors of PDE7 and PDE4. WO02088080; 2002
    • Bristol-Myers Squibb. Dual inhibitors of PDE7 and PDE4. WO02088080; 2002
  • 78
    • 56349140475 scopus 로고    scopus 로고
    • Dual inhibitors of PDE7 and PDE4
    • US 20030104974;
    • Bristol-Myers Squibb. Dual inhibitors of PDE7 and PDE4. US 20030104974; 2003
    • (2003)
    • Squibb, B.-M.1
  • 79
    • 56349136236 scopus 로고    scopus 로고
    • Altana Pharma AG. Novel phthalazinones. WO02085906; 2002
    • Altana Pharma AG. Novel phthalazinones. WO02085906; 2002
  • 80
    • 45949101641 scopus 로고    scopus 로고
    • CODES, a novel procedure for ligand-based virtual screening: PDE7 inhibitors as an application example
    • Castro A, Jerez MJ, Gil C, et al. CODES, a novel procedure for ligand-based virtual screening: PDE7 inhibitors as an application example. Eur J Med Chem 2008;43:1349-59
    • (2008) Eur J Med Chem , vol.43 , pp. 1349-1359
    • Castro, A.1    Jerez, M.J.2    Gil, C.3
  • 81
    • 56349154790 scopus 로고    scopus 로고
    • Consejo Superior de Investigaciones Científicas and Instituto de Salud Carlos III. Compuesto inhibidor dual de las enzimas PDE7 y/o PDE4, composiciones farmacéuticas y sus aplicaciones. EP200700762; 2007
    • Consejo Superior de Investigaciones Científicas and Instituto de Salud Carlos III. Compuesto inhibidor dual de las enzimas PDE7 y/o PDE4, composiciones farmacéuticas y sus aplicaciones. EP200700762; 2007
  • 82
    • 0036225637 scopus 로고    scopus 로고
    • PDE7 inhibitors
    • Celltech Chiroscience Ltd. WO0174786
    • Celltech Chiroscience Ltd. WO0174786. PDE7 inhibitors. Expert Opin Ther Patents 2002;12:601-3
    • (2002) Expert Opin Ther Patents , vol.12 , pp. 601-603


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.