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Volumn 16, Issue 10, 2007, Pages 1585-1599

Small-molecule inhibitors of PDE-IV and -VII in the treatment of respiratory diseases and chronic inflammation

Author keywords

Asthma; COPD; PDE IV; PDE VII; Respiratory diseases

Indexed keywords

2 METHYL 5 NITROBENZENESULFONIC ACID DIMETHYLAMIDE; BENZOTHIADIAZINE DERIVATIVE; BMS 586853; CC 10004; CILOMILAST; GABAPENTIN; N (3,5 DICHLORO 4 PYRIDYL) [1 (4 FLUOROBENZYL) 5 HYDROXY 3 INDOLYL]GLYOXYLIC ACID AMIDE; OGLEMILAST; ONO 6126; PHOSPHODIESTERASE INHIBITOR; PHOSPHODIESTERASE IV; PHOSPHODIESTERASE IV INHIBITOR; PHOSPHODIESTERASE VII; PHOSPHODIESTERASE VII INHIBITOR; PURINE NUCLEOTIDE; PURINE NUCLEOTIDE DERIVATIVE; PYRIMIDINE NUCLEOTIDE; PYRIMIDINE NUCLEOTIDE DERIVATIVE; PYRROLOPYRIMIDINE DERIVATIVE; QUINAZOLINONE DERIVATIVE; ROFLUMILAST; ROLIPRAM; SPIROQUINAZOLINONE DERIVATIVE; SULFONAMIDE; THEOPHYLLINE; THIADIAZOLE DERIVATIVE; TOFIMILAST; TPI 1100; UNCLASSIFIED DRUG; UNINDEXED DRUG; YM 393059; 3',5' CYCLIC NUCLEOTIDE PHOSPHODIESTERASE; CYCLIC NUCLEOTIDE PHOSPHODIESTERASES, TYPE 4; PHOSPHODIESTERASE-7;

EID: 35248887662     PISSN: 13543784     EISSN: None     Source Type: Journal    
DOI: 10.1517/13543784.16.10.1585     Document Type: Review
Times cited : (21)

References (53)
  • 1
    • 0034024182 scopus 로고    scopus 로고
    • Phosphodiesterase 4 inhibitors and the treatment of asthma; where we are now and where do we go from here?
    • GIEMBYCZ MA: Phosphodiesterase 4 inhibitors and the treatment of asthma; where we are now and where do we go from here? Drugs (2000) 59:193-212.
    • (2000) Drugs , vol.59 , pp. 193-212
    • GIEMBYCZ, M.A.1
  • 2
    • 14244270585 scopus 로고    scopus 로고
    • Development status of second-generation PDE4 inhibitors forasthma and COPD: The story so far?
    • GIEMBYCZ MA: Development status of second-generation PDE4 inhibitors forasthma and COPD: the story so far? Monaldi. Arch. Chest Dis. (2002) 57:48-64.
    • (2002) Monaldi. Arch. Chest Dis , vol.57 , pp. 48-64
    • GIEMBYCZ, M.A.1
  • 4
    • 2542487257 scopus 로고    scopus 로고
    • the toxicity of SCH 351591, a novel phosphodiesterase 4B inhibitor, in cynomolgus monkeys
    • LOSCO PE, EVANS EW, BARAT SA et al.: the toxicity of SCH 351591, a novel phosphodiesterase 4B inhibitor, in cynomolgus monkeys. Toxicol. Pathol. (2004) 32(3):295-308.
    • (2004) Toxicol. Pathol , vol.32 , Issue.3 , pp. 295-308
    • LOSCO, P.E.1    EVANS, E.W.2    BARAT, S.A.3
  • 5
    • 33644824002 scopus 로고    scopus 로고
    • Mesentritis precedes vasculitis in the rat mesentry after subacute administration of a phosphodiesterase type 4 inhibitor
    • MECKLENBERG L, HEUSER A, JUENGLING T et al.: Mesentritis precedes vasculitis in the rat mesentry after subacute administration of a phosphodiesterase type 4 inhibitor. Toxicol. Lett. (2006) 163(1):54-64.
    • (2006) Toxicol. Lett , vol.163 , Issue.1 , pp. 54-64
    • MECKLENBERG, L.1    HEUSER, A.2    JUENGLING, T.3
  • 6
    • 21744438149 scopus 로고    scopus 로고
    • Identification and characterization of PDE4A11, a novel, widely expressed long isoform encoded by the human PDE4A cAMP phosphodiesterases gene
    • WALLACE DA, JOHNSTON LA, HUSTON E et al.: Identification and characterization of PDE4A11, a novel, widely expressed long isoform encoded by the human PDE4A cAMP phosphodiesterases gene. Mol. Pharmacol. (2005) 67:1920-1934.
    • (2005) Mol. Pharmacol , vol.67 , pp. 1920-1934
    • WALLACE, D.A.1    JOHNSTON, L.A.2    HUSTON, E.3
  • 7
    • 0030697068 scopus 로고    scopus 로고
    • Molecular cloning and transient expression in COS cells of a novel human PDE4B cAMP specific phosphodiesterase HSPDE4B3
    • HUSTON E, LUMB S, RUSSELL A et a;.: Molecular cloning and transient expression in COS cells of a novel human PDE4B cAMP specific phosphodiesterase HSPDE4B3. Biochem. J. (1997) 328(Part 2):549-558.
    • (1997) Biochem. J , vol.328 , Issue.PART 2 , pp. 549-558
    • HUSTON, E.1    LUMB, S.2    RUSSELL, A.3    et a4
  • 8
    • 0035030692 scopus 로고    scopus 로고
    • Molecular cloning, genomic positioning, promoter identification and characterization of the novel cAMP specific phosphodiesterase PDE4A10
    • RENA G, BEGG F, ROSS A et al.: Molecular cloning, genomic positioning, promoter identification and characterization of the novel cAMP specific phosphodiesterase PDE4A10. Mol. Pharmacol. (2001) 59:995-1011.
    • (2001) Mol. Pharmacol , vol.59 , pp. 995-1011
    • RENA, G.1    BEGG, F.2    ROSS, A.3
  • 9
    • 0037188511 scopus 로고    scopus 로고
    • Induction of the cyclic nucleotide phosphodiesterase PDE4B is essential for LPS-activated TNF-α responses
    • JIN SL, CONTI M: Induction of the cyclic nucleotide phosphodiesterase PDE4B is essential for LPS-activated TNF-α responses. Proc. Natl. Acad. Sci. USA (2002) 99(11):7628-7633.
    • (2002) Proc. Natl. Acad. Sci. USA , vol.99 , Issue.11 , pp. 7628-7633
    • JIN, S.L.1    CONTI, M.2
  • 10
    • 11844267183 scopus 로고    scopus 로고
    • Phosphodiesterase-4 inhibitors for asthma and chronic obstructive pulmonary disease
    • LIPWORTH BJ: Phosphodiesterase-4 inhibitors for asthma and chronic obstructive pulmonary disease. Lancet (2005) 365(9454):167-175.
    • (2005) Lancet , vol.365 , Issue.9454 , pp. 167-175
    • LIPWORTH, B.J.1
  • 11
    • 0030702945 scopus 로고    scopus 로고
    • Human recombinant phosphodiesterase 4B2B binds (R) - rolipram at a single site with two affinities
    • ROCQUE WJ, TAIN J, WISEMAN JS et al.: Human recombinant phosphodiesterase 4B2B binds (R) - rolipram at a single site with two affinities. Biochemistry (1997) 36(46):14250-14261.
    • (1997) Biochemistry , vol.36 , Issue.46 , pp. 14250-14261
    • ROCQUE, W.J.1    TAIN, J.2    WISEMAN, J.S.3
  • 12
    • 0029939872 scopus 로고    scopus 로고
    • Association of the anti-inflammatory activity of phosphodiesterase 4 (PDE4) inhibitors with either inhibition of PDE4 catalytic activity or competetion for [3H] rolipram. binding
    • BARNETTE MS, BARTUS JO, BURMAN M et al.: Association of the anti-inflammatory activity of phosphodiesterase 4 (PDE4) inhibitors with either inhibition of PDE4 catalytic activity or competetion for [3H] rolipram. binding. J. Biochem. Pharmacol. (1996) 51(7):949-956.
    • (1996) J. Biochem. Pharmacol , vol.51 , Issue.7 , pp. 949-956
    • BARNETTE, M.S.1    BARTUS, J.O.2    BURMAN, M.3
  • 13
    • 0036790480 scopus 로고    scopus 로고
    • Deletion of phoshodiesterase 4D in mice shortens α(2)-adrenoceptor mediated anesthesia, a behavioural correlate of emesis
    • ROBICHAUD A, STAMATIOU PB, JIN SL et al.: Deletion of phoshodiesterase 4D in mice shortens α(2)-adrenoceptor mediated anesthesia, a behavioural correlate of emesis. J. Clin. Invest. (2002) 110(7):1045-1052.
    • (2002) J. Clin. Invest , vol.110 , Issue.7 , pp. 1045-1052
    • ROBICHAUD, A.1    STAMATIOU, P.B.2    JIN, S.L.3
  • 14
    • 26244467287 scopus 로고    scopus 로고
    • Phoshodiesterase 4D deficiency in the ryanodine receptor complex promotes heart failure and arrhythmias
    • LENHART SE, WEHRENS XHT, REIKEN S et al.: Phoshodiesterase 4D deficiency in the ryanodine receptor complex promotes heart failure and arrhythmias. Cell (2005) 123:25-35.
    • (2005) Cell , vol.123 , pp. 25-35
    • LENHART, S.E.1    WEHRENS, X.H.T.2    REIKEN, S.3
  • 15
    • 27644589238 scopus 로고    scopus 로고
    • Phosphodiesterase-4 selective and dual-specificity inhibitors for the therapy of chronic obstructive pulmonary disease
    • GIEMBYCZ MA: Phosphodiesterase-4 selective and dual-specificity inhibitors for the therapy of chronic obstructive pulmonary disease. Proc. Am. Thorac. Soc. (2005) 2:333-336.
    • (2005) Proc. Am. Thorac. Soc , vol.2 , pp. 333-336
    • GIEMBYCZ, M.A.1
  • 16
    • 23744451716 scopus 로고    scopus 로고
    • Roflumilast - an oral anti-inflammatory treatment for chronic obstructive pulmonary disease: A randomized controlled trial
    • RABE KF, BATEMAN ED, O'DONNEL D, WITTE S, BREDEBBROKER D, BETHKE TD: Roflumilast - an oral anti-inflammatory treatment for chronic obstructive pulmonary disease: A randomized controlled trial. Lancet (2005) 366(9485):563-571.
    • (2005) Lancet , vol.366 , Issue.9485 , pp. 563-571
    • RABE, K.F.1    BATEMAN, E.D.2    O'DONNEL, D.3    WITTE, S.4    BREDEBBROKER, D.5    BETHKE, T.D.6
  • 17
    • 33646847170 scopus 로고    scopus 로고
    • Roflumilast for the treatment of chronic obstructive pulmonary disease
    • SABINA AA. Roflumilast for the treatment of chronic obstructive pulmonary disease. Curr. Opin. Investig. Drugs (2006) 7(5):412-417.
    • (2006) Curr. Opin. Investig. Drugs , vol.7 , Issue.5 , pp. 412-417
    • SABINA, A.A.1
  • 18
    • 35649010747 scopus 로고    scopus 로고
    • LEICHTL S, SCHMID-WIRLITSCH C, BREDENBROKER D et al.: Dose-related efficacy of once-daily roflumilast, a new orally active, selective phosphodiesterase 4 inhibitor, in asthma. Am. J. Respir. Crit. Care Med. (2002) 165(8)-A185.
    • LEICHTL S, SCHMID-WIRLITSCH C, BREDENBROKER D et al.: Dose-related efficacy of once-daily roflumilast, a new orally active, selective phosphodiesterase 4 inhibitor, in asthma. Am. J. Respir. Crit. Care Med. (2002) 165(8)-A185.
  • 19
    • 23244467556 scopus 로고    scopus 로고
    • Roflumilast, an oral, once-daily phosphodiesterase 4 inhibitor, attenuates allergen-induced asthmatic reactions
    • VAN SCHALKWYK E, STRYDOM K, WILLIAMS Z et al.: Roflumilast, an oral, once-daily phosphodiesterase 4 inhibitor, attenuates allergen-induced asthmatic reactions. J. Allergy Clin. Immunol. (2005) 116:292-298.
    • (2005) J. Allergy Clin. Immunol , vol.116 , pp. 292-298
    • VAN SCHALKWYK, E.1    STRYDOM, K.2    WILLIAMS, Z.3
  • 20
    • 14444268769 scopus 로고    scopus 로고
    • 1,4-Cyclohcxanecarboxylates: Potent and selective inhibitors of phosophodiesterasc 4 for the treatment of asthma
    • CHRISTENSEN SB, GUIDER A, FORSTER CJ et al.: 1,4-Cyclohcxanecarboxylates: potent and selective inhibitors of phosophodiesterasc 4 for the treatment of asthma. J. Med. Chem. (1998) 41(6):821-835.
    • (1998) J. Med. Chem , vol.41 , Issue.6 , pp. 821-835
    • CHRISTENSEN, S.B.1    GUIDER, A.2    FORSTER, C.J.3
  • 21
    • 0035963952 scopus 로고    scopus 로고
    • Cilomilast a selective PDE4 inhibitor for the treatment of patients with chronic obstructive pulmonary disease: A randomized dose ranging study
    • COMPTON CH, CUBB J, NEIMAN R et al.: Cilomilast a selective PDE4 inhibitor for the treatment of patients with chronic obstructive pulmonary disease: a randomized dose ranging study. Lancet (2001) 358:265-270.
    • (2001) Lancet , vol.358 , pp. 265-270
    • COMPTON, C.H.1    CUBB, J.2    NEIMAN, R.3
  • 22
    • 28844444678 scopus 로고    scopus 로고
    • Cilomast (Ariflo) 15 mg bid safety in a 6-month clinical trial program
    • San Francisco, USA 18, 23 May
    • COMPTON C, EDELSON J, CEDAR E et al.: Cilomast (Ariflo) 15 mg bid safety in a 6-month clinical trial program. 97th American Thoracic Society Meeting. San Francisco, USA (18 - 23 May 2001).
    • (2001) 97th American Thoracic Society Meeting
    • COMPTON, C.1    EDELSON, J.2    CEDAR, E.3
  • 23
    • 33748267734 scopus 로고    scopus 로고
    • An update and appraisal of the cilomilast Phase III clinical development programme for chronic obstructive pulmonary disease
    • GEIMBYCZ MA: An update and appraisal of the cilomilast Phase III clinical development programme for chronic obstructive pulmonary disease. Br. J. Clin. Pharmacol. (2006):1-15.
    • (2006) Br. J. Clin. Pharmacol , pp. 1-15
    • GEIMBYCZ, M.A.1
  • 24
    • 18144409360 scopus 로고    scopus 로고
    • CC-10004: A novel PDE4 inhibitor with an improved therapeutic index
    • London, UK 10-11 March
    • SCHAFER P: CC-10004: a novel PDE4 inhibitor with an improved therapeutic index. SMI Conference - Chronic Obstructive Pulmonary Disorders. London, UK (10-11 March 2004).
    • (2004) SMI Conference - Chronic Obstructive Pulmonary Disorders
    • SCHAFER, P.1
  • 25
    • 28844448922 scopus 로고    scopus 로고
    • A novel PDE4 inhibitory agent with endothelial cell specific activity
    • Abstract 2372
    • ROSEN J, MILLER W, HE M et al.: A novel PDE4 inhibitory agent with endothelial cell specific activity. Proc. Am. Assoc. Cancer Res. (2004) 45:(Abstract 2372).
    • (2004) Proc. Am. Assoc. Cancer Res , vol.45
    • ROSEN, J.1    MILLER, W.2    HE, M.3
  • 26
    • 18144409148 scopus 로고    scopus 로고
    • KHOBZAOUI M, GUTKE HJ, BURNET M: Cc-10004. Curr. Opin. Investig. Drugs (2005) 6(5):518-525.
    • KHOBZAOUI M, GUTKE HJ, BURNET M: Cc-10004. Curr. Opin. Investig. Drugs (2005) 6(5):518-525.
  • 27
    • 22744449499 scopus 로고    scopus 로고
    • Pharmacological profile of Ono-6126, a novel phosphodiesterase 4 (PDE4) inhibitor
    • Atlanta, USA 17-22 May
    • TAKEDA H, AL E: Pharmacological profile of Ono-6126, a novel phosphodiesterase 4 (PDE4) inhibitor. 98th International Conference of the American Thoracic Society. Atlanta, USA (17-22 May 2002).
    • (2002) 98th International Conference of the American Thoracic Society
    • TAKEDA, H.1    AL, E.2
  • 28
    • 0345821007 scopus 로고    scopus 로고
    • Suppressive effect of novel phosphodiesterase 4 (PDE4) inhibitor Ono-6126 on TNF-α release was increased after repeated oral administration in healthy Japanese subjects
    • Abstract 2557
    • FURUIE H, NAKAGAWA S, KAWASHIMA M, AL E: Suppressive effect of novel phosphodiesterase 4 (PDE4) inhibitor Ono-6126 on TNF-α release was increased after repeated oral administration in healthy Japanese subjects. Eur. Respir J. (2003) (Suppl. 45):(Abstract 2557).
    • (2003) Eur. Respir J , Issue.SUPPL. 45
    • FURUIE, H.1    NAKAGAWA, S.2    KAWASHIMA, M.3    AL, E.4
  • 29
    • 28844481149 scopus 로고    scopus 로고
    • The pharmacological and safety profile of the PDE4 inhibitor GRC-3886
    • Glasgow, UK 4-8 September
    • VAKKALANKA S: The pharmacological and safety profile of the PDE4 inhibitor GRC-3886. 14th Annual European Respiratory Society Congress. Glasgow, UK (4-8 September 2004).
    • (2004) 14th Annual European Respiratory Society Congress
    • VAKKALANKA, S.1
  • 30
    • 33846455467 scopus 로고    scopus 로고
    • SAR of a series of 5,6-dihydro-(9H)-pyrazolo[3,4-c]- 1,2,4-triazolo[4,3-α]pyridines as potent inhibitors of human eosinophil phosphodiesterase
    • DUPLANTIER AJ, BACHERT EL, CHENG CB et al.: SAR of a series of 5,6-dihydro-(9H)-pyrazolo[3,4-c]- 1,2,4-triazolo[4,3-α]pyridines as potent inhibitors of human eosinophil phosphodiesterase. J. Med. Chem. (2007) 50(2):344-349.
    • (2007) J. Med. Chem , vol.50 , Issue.2 , pp. 344-349
    • DUPLANTIER, A.J.1    BACHERT, E.L.2    CHENG, C.B.3
  • 31
    • 1242268903 scopus 로고    scopus 로고
    • Anti-inflammatory potential of the selective phosphodiesterase 4 inhibitor N-(3,5-dichloro-pyrid-4-yl)-[1-(4-fluorobenzyl) -5-hydroxy-indole-3-yl]- glyoxylic acid amide (AWD 12-281), in human cell preparations
    • DRAHEIM R, EGERLAND U, RUNDFELDT C: Anti-inflammatory potential of the selective phosphodiesterase 4 inhibitor N-(3,5-dichloro-pyrid-4-yl)-[1-(4-fluorobenzyl) -5-hydroxy-indole-3-yl]- glyoxylic acid amide (AWD 12-281), in human cell preparations. J. Pbarmacol. Exp. Ther. (2004) 308(2):555-563.
    • (2004) J. Pbarmacol. Exp. Ther , vol.308 , Issue.2 , pp. 555-563
    • DRAHEIM, R.1    EGERLAND, U.2    RUNDFELDT, C.3
  • 33
    • 0027164208 scopus 로고
    • Isolation and characterizaton of a previously undetected cAMP specific phosphodiesterase by complcmentation of a cAMP phosphodiesterase deficient Saccharomyces cerevisiae
    • MICHAELI T, BLOOM TG, MARTINS T et al.: Isolation and characterizaton of a previously undetected cAMP specific phosphodiesterase by complcmentation of a cAMP phosphodiesterase deficient Saccharomyces cerevisiae. J. Biol. Chem. (1993) 268:12925-12932.
    • (1993) J. Biol. Chem , vol.268 , pp. 12925-12932
    • MICHAELI, T.1    BLOOM, T.G.2    MARTINS, T.3
  • 34
    • 0030971045 scopus 로고    scopus 로고
    • Alternative splicing of the high affinity cAMP specific phosphodiesterase (PDE7A) mRNA in human skeletal muscle and heart
    • HAN P, ZHU XY, MICHAELI T: Alternative splicing of the high affinity cAMP specific phosphodiesterase (PDE7A) mRNA in human skeletal muscle and heart. J. Biol. Chem. (1997). 272:16152-16157.
    • (1997) J. Biol. Chem , vol.272 , pp. 16152-16157
    • HAN, P.1    ZHU, X.Y.2    MICHAELI, T.3
  • 36
    • 0029833842 scopus 로고    scopus 로고
    • Identification of cyclic AMP phosphodiesterases 3, 4 and 7 in human CD4 and CD8 T-lymphocytes: Role in regulating proliferation and the biosynthesis of interleukin-2
    • GIEMBYCZ MA, CORRIGAN CJ, SEYBOLD J, NEWTON R, BARNES PJ: Identification of cyclic AMP phosphodiesterases 3, 4 and 7 in human CD4 and CD8 T-lymphocytes: role in regulating proliferation and the biosynthesis of interleukin-2. Br. J. Pharmacol. (1996) 118:1945-1958.
    • (1996) Br. J. Pharmacol , vol.118 , pp. 1945-1958
    • GIEMBYCZ, M.A.1    CORRIGAN, C.J.2    SEYBOLD, J.3    NEWTON, R.4    BARNES, P.J.5
  • 37
    • 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(5403):848-851.
    • (1999) Science , vol.283 , Issue.5403 , pp. 848-851
    • LI, L.1    YEE, C.2    BEAVO, J.A.3
  • 38
    • 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(12):6414-6420.
    • (2003) J. Immunol , vol.171 , Issue.12 , pp. 6414-6420
    • YANG, G.1    MCINTYRE, K.W.2    TOWNSEND, R.M.3
  • 40
    • 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) 14:2955-2958.
    • (2004) Bioorg. Med. Chem. Lett , vol.14 , pp. 2955-2958
    • PITTS, W.J.1    VACCARO, W.2    HUYNH, T.3
  • 41
    • 20144366973 scopus 로고    scopus 로고
    • Fused pyrimidine based inhibitors of phosphodiesterase 7 (PDE7): Synthesis and structure-activity relationships
    • KEMPSON J, MARINIER A, DODIER M et al.: Fused pyrimidine based inhibitors of phosphodiesterase 7 (PDE7): synthesis and structure-activity relationships. Bioorg. Med. Chem. Lett. (2005) 15:1829-1833.
    • (2005) Bioorg. Med. Chem. Lett , vol.15 , pp. 1829-1833
    • KEMPSON, J.1    MARINIER, A.2    DODIER, M.3
  • 42
    • 35648960661 scopus 로고    scopus 로고
    • Identification and SAR of potent inhibitors of phosphodiesterase 7 (PDE7)
    • Philadelphia, USA 22, 26 August
    • GUO J, CARLSEN M, BARBOSA J: Identification and SAR of potent inhibitors of phosphodiesterase 7 (PDE7). 228th ACS Meeting. Philadelphia, USA (22 - 26 August 2004).
    • (2004) 228th ACS Meeting
    • GUO, J.1    CARLSEN, M.2    BARBOSA, J.3
  • 43
    • 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(8):1081-1083.
    • (2001) Bioorg. Med. Chem. Lett , vol.11 , Issue.8 , pp. 1081-1083
    • BARNES, M.J.1    COOPER, N.2    DAVENPORT, R.J.3
  • 44
    • 0343986277 scopus 로고    scopus 로고
    • Benzyl derivatives of 2,1,3-benzo-and benzothicno [3,2-a] thiadiazine 2,2-dioxides: First phosphodiesterase 7 inhibitors
    • MARTINEZ A, CASTRO A, GIL C et al.: Benzyl derivatives of 2,1,3-benzo-and benzothicno [3,2-a] thiadiazine 2,2-dioxides: first phosphodiesterase 7 inhibitors. J. Med. Chem. (2000) 43:683-689.
    • (2000) J. Med. Chem , vol.43 , pp. 683-689
    • MARTINEZ, A.1    CASTRO, A.2    GIL, C.3
  • 45
    • 0034924329 scopus 로고    scopus 로고
    • CoMFA of benzyl derivatives of 2,1,3-benzo and benzothieno [3,2-α] thiadiazine 2,2-dioxides: Clues for the design of phosphodiesterase 7 inhibitors
    • CASTRO A, ABASOLO MI, GIL C, SEGARRA V, MARTINEZ A: CoMFA of benzyl derivatives of 2,1,3-benzo and benzothieno [3,2-α] thiadiazine 2,2-dioxides: clues for the design of phosphodiesterase 7 inhibitors. Eur. J. Med. Chem. (2001) 36:333-338.
    • (2001) Eur. J. Med. Chem , vol.36 , pp. 333-338
    • CASTRO, A.1    ABASOLO, M.I.2    GIL, C.3    SEGARRA, V.4    MARTINEZ, A.5
  • 46
    • 8544250603 scopus 로고    scopus 로고
    • Discovery of thiadiazoles as a novel structural class of potent and selective PDE7 inhibitors. 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. 1. Design, synthesis and structure-activity relationship studies. Bioorg. Med. Chem. Lett. (2004) 14:4607-4613.
    • (2004) Bioorg. Med. Chem. Lett , vol.14 , pp. 4607-4613
    • VERGNE, F.1    BERNARDELLI, P.2    LORTHIOIS, E.3
  • 47
    • 8544256308 scopus 로고    scopus 로고
    • Discovery of thiadiazoles as a novel structural class of potent and selective PDE7 inhibitors. 2. Metabolism directed optmization 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. 2. Metabolism directed optmization studies towards orally bioavailable derivatives. Bioorg. Med. Chem. Lett. (2004) 14:4615-4621.
    • (2004) Bioorg. Med. Chem. Lett , vol.14 , pp. 4615-4621
    • VERGNE, F.1    BERNARDELLI, P.2    LORTHIOIS, E.3
  • 48
    • 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) 14:4623-4626.
    • (2004) Bioorg. Med. Chem. Lett , vol.14 , pp. 4623-4626
    • LORTHIOIS, E.1    BERNARDELLI, P.2    VERGNE, F.3
  • 49
    • 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) 14:4627-4631.
    • (2004) Bioorg. Med. Chem. Lett , vol.14 , pp. 4627-4631
    • BERNARDELLI, P.1    LORTHIOIS, E.2    VERGNE, F.3
  • 50
    • 35648992829 scopus 로고    scopus 로고
    • A novel class of PDE inhibitors
    • HUNT H: A novel class of PDE inhibitors. Trends Med. Chem. (2000).
    • (2000) Trends Med. Chem
    • HUNT, H.1
  • 51
    • 35648953634 scopus 로고    scopus 로고
    • Trends in medicinal chemistry - SMR symposium
    • Glaxo Wellcome Research & Development,Stevenage UK, 30 November
    • BROVIN H: IDDB Meeting Report Trends in medicinal chemistry - SMR symposium-Glaxo Wellcome Research & Development,Stevenage UK. (30 November 2000).
    • (2000) IDDB Meeting Report
    • BROVIN, H.1
  • 52
    • 33749986292 scopus 로고    scopus 로고
    • Pharmacological profile of a novel phosphodiesterase 7A and -4 dual inhibitor, YM-393059, on acute and chronic inflammation models
    • YAMAMOTO S, SUGAHARA S, IKEDA K, SHIMIZU Y. Pharmacological profile of a novel phosphodiesterase 7A and -4 dual inhibitor, YM-393059, on acute and chronic inflammation models. Eur. J. Pharm. (2006) 550(1-3):166-172.
    • (2006) Eur. J. Pharm , vol.550 , Issue.1-3 , pp. 166-172
    • YAMAMOTO, S.1    SUGAHARA, S.2    IKEDA, K.3    SHIMIZU, Y.4
  • 53
    • 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. Pharm. (2006) 541(1-2):106-114.
    • (2006) Eur. J. Pharm , vol.541 , Issue.1-2 , pp. 106-114
    • YAMAMOTO, S.1    SUGAHARA, S.2    NAITO, R.3


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