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Volumn 48, Issue 21, 2005, Pages 6523-6543

Designed multiple ligands. An emerging drug discovery paradigm

Author keywords

[No Author keywords available]

Indexed keywords

1 (2,3 DIHYDRO 1 METHYL 2 OXO 5 PHENYL 1H 1,4 BENZODIAZEPIN 3 YL) 3 (3 METHYLPHENYL)UREA; 3,4 DICHLORO N METHYL N [1 PHENYL 2 (1 PYRROLIDINYL)ETHYL]BENZENEACETAMIDE; 5 (2,4 DIOXO 5 THIAZOLIDINYLMETHYL) 2 METHOXY N [4 (TRIFLUOROMETHYL)BENZYL]BENZAMIDE; 6 [[3 FLUORO 5 (3,4,5,6 TETRAHYDRO 4 METHOXY 2H PYRAN 4 YL)]PHENOXYMETHYL] 1 METHYL 2 QUINOLONE; 6 HYDROXY 4,5,7 TRIMETHYL 2 (4 SULFAMOYLBENZYLAMINO)BENZOTHIAZOLE; 6 HYDROXY 5,7 DIMETHYL 2 METHYLAMINO 4 (3 PYRIDYLMETHYL)BENZOTHIAZOLE; ACETYLSALICYLIC ACID 3 (NITROXYMETHYL)PHENYL ESTER; AGMATINE; AMITRIPTYLINE; AMLODIPINE; AMLODIPINE PLUS ATORVASTATIN; ANTITHROMBOCYTIC AGENT; ATORVASTATIN; CELECOXIB; CETIRIZINE; CMI 977; CYCLOOXYGENASE 2 INHIBITOR; DARBUFELONE; DOPAMINE 2 RECEPTOR BLOCKING AGENT; DULOXETINE; EZETIMIBE; EZETIMIBE PLUS SIMVASTATIN; FENTANYL DERIVATIVE; FLUOXETINE; IMATINIB; MILNACIPRAN; N (2 MERCAPTOMETHYL 3 PHENYLPROPIONYL) BETA ALANINE; NEUROLEPTIC AGENT; OLANZAPINE; OPIATE; PINDOLOL; PRIFELONE; QUETIAPINE; RISPERIDONE; RUPATADINE; SB 649915; SIMVASTATIN; TRICYCLIC ANTIDEPRESSANT AGENT; TROPISETRON; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 27144449695     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm058225d     Document Type: Review
Times cited : (1135)

References (108)
  • 1
    • 4644271084 scopus 로고    scopus 로고
    • Magic shotguns versus magic bullets: Selectively non-selective drugs for mood disorders and schizophrenia
    • Roth, B. L.; Sheffler, D. J.; Kroeze, W. K. Magic shotguns versus magic bullets: selectively non-selective drugs for mood disorders and schizophrenia. Nat. Rev. Drug Discovery 2004, 3, 353-359.
    • (2004) Nat. Rev. Drug Discovery , vol.3 , pp. 353-359
    • Roth, B.L.1    Sheffler, D.J.2    Kroeze, W.K.3
  • 2
    • 0037490085 scopus 로고    scopus 로고
    • Value of low dose combination treatment with blood pressure lowering drugs: Analysis of 354 randomised trials
    • Law, M. R.; Wald, J.; Morris, J. K.; Jordan, R. E. Value of low dose combination treatment with blood pressure lowering drugs: analysis of 354 randomised trials. Br. Med. J. 2003, 326, 1427-1431.
    • (2003) Br. Med. J. , vol.326 , pp. 1427-1431
    • Law, M.R.1    Wald, J.2    Morris, J.K.3    Jordan, R.E.4
  • 4
    • 0029914669 scopus 로고    scopus 로고
    • Mobilization of peripheral blood progenitor cells following CHOP treatment combined with delayed granulocyte colony-stimulating factor administration in patients with non-Hodgkin's lymphoma
    • Takano, H.; Sawada, K.; Sato, N.; Natoya, A.; Tarumi, T.; Hirayama, S.; Koizumi, K.; Takahashi, T. A.; Sekiguchi, S.; Koike, T. Mobilization of peripheral blood progenitor cells following CHOP treatment combined with delayed granulocyte colony-stimulating factor administration in patients with non-Hodgkin's lymphoma. Leuk. Lymphoma 1996, 21, 473-478.
    • (1996) Leuk. Lymphoma , vol.21 , pp. 473-478
    • Takano, H.1    Sawada, K.2    Sato, N.3    Natoya, A.4    Tarumi, T.5    Hirayama, S.6    Koizumi, K.7    Takahashi, T.A.8    Sekiguchi, S.9    Koike, T.10
  • 5
    • 0029028067 scopus 로고
    • Potential mechanism for sustained antiretroviral effiacy of AZT-3TC combination therapy
    • Larder, B. A.; Kemp, S. D.; Harrigan, P. R. Potential mechanism for sustained antiretroviral effiacy of AZT-3TC combination therapy. Science 1995, 269, 696-699.
    • (1995) Science , vol.269 , pp. 696-699
    • Larder, B.A.1    Kemp, S.D.2    Harrigan, P.R.3
  • 7
    • 0034657439 scopus 로고    scopus 로고
    • Combination antihypertensive drugs: Recommendations for use
    • Skolnik, N. S.; Beck, J. D.; Clark, M. Combination antihypertensive drugs: Recommendations for use. Am. Fam. Physician 2000, 61, 3049-3056.
    • (2000) Am. Fam. Physician , vol.61 , pp. 3049-3056
    • Skolnik, N.S.1    Beck, J.D.2    Clark, M.3
  • 8
    • 4544265949 scopus 로고    scopus 로고
    • Cardiovascular combinations
    • Glass, G. Cardiovascular combinations. Nat. Rev. Drug Discovery 2004, 3, 731-732.
    • (2004) Nat. Rev. Drug Discovery , vol.3 , pp. 731-732
    • Glass, G.1
  • 9
    • 3242794178 scopus 로고    scopus 로고
    • From magic bullets to designed multiple ligands
    • Morphy, R.; Kay, C.; Rankovic, Z. From magic bullets to designed multiple ligands. Drug Discovery Today 2004, 9, 641-651.
    • (2004) Drug Discovery Today , vol.9 , pp. 641-651
    • Morphy, R.1    Kay, C.2    Rankovic, Z.3
  • 10
    • 4544230271 scopus 로고    scopus 로고
    • Amlodipine/atorvastatin: The first cross risk factor polypill for the prevention and treatment of cardiovascular disease
    • Frishman, W. H.; Zuckerman, A. L. Amlodipine/atorvastatin: the first cross risk factor polypill for the prevention and treatment of cardiovascular disease. Expert Rev. Cardiovas. Ther. 2004, 2, 675-681.
    • (2004) Expert Rev. Cardiovas. Ther. , vol.2 , pp. 675-681
    • Frishman, W.H.1    Zuckerman, A.L.2
  • 11
    • 16644395416 scopus 로고    scopus 로고
    • Ezetimibe + simvastatin (Merck/Schering-Plough)
    • Flores, N. A. Ezetimibe + simvastatin (Merck/Schering-Plough). Curr. Opin. Invest. Drugs 2004, 5, 984-992.
    • (2004) Curr. Opin. Invest. Drugs , vol.5 , pp. 984-992
    • Flores, N.A.1
  • 12
    • 0034619028 scopus 로고    scopus 로고
    • Adverse drug reactions: Definitions, diagnosis and management
    • Edwards, I. R.; Aronson, J. K. Adverse drug reactions: Definitions, diagnosis and management. Lancet 2000, 356, 1255-1259.
    • (2000) Lancet , vol.356 , pp. 1255-1259
    • Edwards, I.R.1    Aronson, J.K.2
  • 13
    • 0031159043 scopus 로고    scopus 로고
    • 4 dopamine receptor antagonist (L-745,870) in acutely psychotic inpatients with schizophrenia
    • 4 dopamine receptor antagonist (L-745,870) in acutely psychotic inpatients with schizophrenia. Arch. Gen. Psychiatry 1997, 54, 567-572.
    • (1997) Arch. Gen. Psychiatry , vol.54 , pp. 567-572
    • Kramer, M.S.1    Last, B.2    Getson, A.3    Reines, S.A.4
  • 16
    • 0037115290 scopus 로고    scopus 로고
    • Comparative Efficacy between venlafaxine and SSRIs: A pooled analysis of patients with depression
    • Stahl, S. M.; Entsuah, R.; Rudolph, R. L. Comparative Efficacy between venlafaxine and SSRIs: A pooled analysis of patients with depression. Biol. Psychiatry 2002, 202, 1166-1174.
    • (2002) Biol. Psychiatry , vol.202 , pp. 1166-1174
    • Stahl, S.M.1    Entsuah, R.2    Rudolph, R.L.3
  • 17
    • 0042574211 scopus 로고    scopus 로고
    • Dual inhibition of cyclooxygenase-2 (COX-2) and 5-lipoxygenase (5-LOX) as a new strategy to provide safer non-steroidal anti-inflammatory drugs
    • Charlier, C.; Michaux, C. Dual inhibition of cyclooxygenase-2 (COX-2) and 5-lipoxygenase (5-LOX) as a new strategy to provide safer non-steroidal anti-inflammatory drugs. Eur. J. Med. Chem. 2003, 38, 645-659.
    • (2003) Eur. J. Med. Chem. , vol.38 , pp. 645-659
    • Charlier, C.1    Michaux, C.2
  • 19
    • 0034730498 scopus 로고    scopus 로고
    • A novel pharmacological approach to treating cardiac ischemia. Binary conjugates of A1 and A3 adenosine receptor agonists
    • Jacobson, K. A.; Xie, R.; Young, L.; Chang, L.; Liang, B. T. A novel pharmacological approach to treating cardiac ischemia. Binary conjugates of A1 and A3 adenosine receptor agonists. J. Biol. Chem. 2000, 275, 30272-30279.
    • (2000) J. Biol. Chem. , vol.275 , pp. 30272-30279
    • Jacobson, K.A.1    Xie, R.2    Young, L.3    Chang, L.4    Liang, B.T.5
  • 20
    • 0035811447 scopus 로고    scopus 로고
    • From models to molecules: Opioid receptor dimers, bivalent ligands, and selective opioid receptor probes
    • Portoghese, P. S. From models to molecules: Opioid receptor dimers, bivalent ligands, and selective opioid receptor probes. J. Med. Chem. 2001, 44, 2259-2269.
    • (2001) J. Med. Chem. , vol.44 , pp. 2259-2269
    • Portoghese, P.S.1
  • 21
    • 15444364860 scopus 로고    scopus 로고
    • A bivalent ligand (KDAN-18) containing δ-antagonist and κ-agonist pharmacophores bridges δ2 and κ1 opioid receptor phenotypes
    • Daniels, D. J.; Kulkarni, A.; Xie, Z.; Bhushan, R. G.; Portoghese, P. S. A bivalent ligand (KDAN-18) containing δ-antagonist and κ-agonist pharmacophores bridges δ2 and κ1 opioid receptor phenotypes. J. Med. Chem. 2005, 48, 1713-1716.
    • (2005) J. Med. Chem. , vol.48 , pp. 1713-1716
    • Daniels, D.J.1    Kulkarni, A.2    Xie, Z.3    Bhushan, R.G.4    Portoghese, P.S.5
  • 28
    • 0037059929 scopus 로고    scopus 로고
    • Design and synthesis of dual inhibitors for matrix metalloproteinase and cathepsin
    • Yamamoto, M.; Ikeda, S.; Kondo, H.; Inoue, S. Design and synthesis of dual inhibitors for matrix metalloproteinase and cathepsin. Bioorg. Med. Chem. Lett. 2002, 12, 375-378.
    • (2002) Bioorg. Med. Chem. Lett. , vol.12 , pp. 375-378
    • Yamamoto, M.1    Ikeda, S.2    Kondo, H.3    Inoue, S.4
  • 33
    • 1642540579 scopus 로고    scopus 로고
    • Unexpected nanomolar inhibition of carbonic anhydrase by COX-2-selective celecoxib: New pharmacological opportunities due to related binding site recognition
    • Weber, A.; Casini, A.; Heine, A.; Kuhn, D.; Supuran, C. T.; Scozzafava, A.; Klebe, G. Unexpected nanomolar inhibition of carbonic anhydrase by COX-2-selective celecoxib: New pharmacological opportunities due to related binding site recognition. J. Med. Chem. 2004, 46, 550-557.
    • (2004) J. Med. Chem. , vol.46 , pp. 550-557
    • Weber, A.1    Casini, A.2    Heine, A.3    Kuhn, D.4    Supuran, C.T.5    Scozzafava, A.6    Klebe, G.7
  • 34
    • 10444280878 scopus 로고    scopus 로고
    • Strategies to overcome resistance to targeted protein kinase inhibitors
    • Daub, H.; Specht, K.; Ullrich, A. Strategies to overcome resistance to targeted protein kinase inhibitors. Nat. Rev. Drug Discovery 2004, 12, 1001-1010.
    • (2004) Nat. Rev. Drug Discovery , vol.12 , pp. 1001-1010
    • Daub, H.1    Specht, K.2    Ullrich, A.3
  • 35
    • 0029951570 scopus 로고    scopus 로고
    • Phenylamino-pyrimidine (PAP) derivatives: A new class of potent and highly selective PDGF-receptor autophosphorylation inhibitors
    • Zimmermann, J.; Buchdunger, E.; Mett, H.; Meyer, T.; Lydon, N.; Traxler, P. Phenylamino-pyrimidine (PAP) derivatives: a new class of potent and highly selective PDGF-receptor autophosphorylation inhibitors. Bioorg. Med. Chem. Lett. 1996, 6, 1221-1226.
    • (1996) Bioorg. Med. Chem. Lett. , vol.6 , pp. 1221-1226
    • Zimmermann, J.1    Buchdunger, E.2    Mett, H.3    Meyer, T.4    Lydon, N.5    Traxler, P.6
  • 36
    • 0031026055 scopus 로고    scopus 로고
    • Potent and selective inhibitors of the Abl-kinase: Phenylamino-pyrimidine (PAP) derivatives
    • Zimmermann, J.; Buchdunger, E.; Mett, H.; Meyer, T.; Lydon, N. B. Potent and selective inhibitors of the Abl-kinase: phenylamino-pyrimidine (PAP) derivatives. Bioorg. Med. Chem. Lett. 1997, 7, 187-192.
    • (1997) Bioorg. Med. Chem. Lett. , vol.7 , pp. 187-192
    • Zimmermann, J.1    Buchdunger, E.2    Mett, H.3    Meyer, T.4    Lydon, N.B.5
  • 37
    • 1642339546 scopus 로고    scopus 로고
    • 7-Alkoxy-4-phenylamino-3-quinolinecarbonitriles as dual inhibitors of Src and Abl kinases
    • Boschelli, D.; Wang, Y.; Johnson, S.; Wu, B.; Ye, F.; Sosa, A.; Golas, J.; Boschelli, F. 7-Alkoxy-4-phenylamino-3-quinolinecarbonitriles as dual inhibitors of Src and Abl kinases. J. Med. Chem. 2004, 47, 1599-1601.
    • (2004) J. Med. Chem. , vol.47 , pp. 1599-1601
    • Boschelli, D.1    Wang, Y.2    Johnson, S.3    Wu, B.4    Ye, F.5    Sosa, A.6    Golas, J.7    Boschelli, F.8
  • 41
    • 27144538941 scopus 로고    scopus 로고
    • The medicinal chemistry journals covered were Bioorg. Med. Chem. Lett., Bioorg. Med. Chem., J. Med. Chem., and Eur. J. Med. Chem.
    • The medicinal chemistry journals covered were Bioorg. Med. Chem. Lett., Bioorg. Med. Chem., J. Med. Chem., and Eur. J. Med. Chem.
  • 42
    • 0030598202 scopus 로고    scopus 로고
    • 1A antagonist WAY-100635 selectively potentiates the presynaptic effects of serotonergic antidepressants in rat brain
    • 1A antagonist WAY-100635 selectively potentiates the presynaptic effects of serotonergic antidepressants in rat brain. Neurosci. Lett. 1996, 219, 123-126.
    • (1996) Neurosci. Lett. , vol.219 , pp. 123-126
    • Romero, L.1    Hervás, I.2    Artigas, F.3
  • 43
    • 0032403624 scopus 로고    scopus 로고
    • Design and synthesis of new potent, silent 5-HT1A antagonists by covalent coupling of aminopropanol derivatives with selective serotonin reuptake inhibitors
    • Perez, M.; Pauwelsb, P.; Pallard-Sigogneaua, I.; Fourriera, C.; Chopinc, P.; Palmierb, C.; Colovrayd, V.; Halazy, S. Design and synthesis of new potent, silent 5-HT1A antagonists by covalent coupling of aminopropanol derivatives with selective serotonin reuptake inhibitors. Bioorg. Med. Chem. Lett. 1998, 8, 3423-3428.
    • (1998) Bioorg. Med. Chem. Lett. , vol.8 , pp. 3423-3428
    • Perez, M.1    Pauwelsb, P.2    Pallard-Sigogneaua, I.3    Fourriera, C.4    Chopinc, P.5    Palmierb, C.6    Colovrayd, V.7    Halazy, S.8
  • 44
    • 0037059917 scopus 로고    scopus 로고
    • Studies toward the discovery of the next generation of antidepressants. Part 2: Incorporating a 5-HT1A antagonist component into a class of serotonin reuptake inhibitors
    • Mewshaw, R.; Meagher, K.; Zhou, P.; Zhou, D.; Shi, X.; Scerni, R.; Smith, D.; Schechter, L.; Andree, T. Studies toward the discovery of the next generation of antidepressants. Part 2: Incorporating a 5-HT1A antagonist component into a class of serotonin reuptake inhibitors. Bioorg. Med. Chem. Lett. 2002, 12, 307-310.
    • (2002) Bioorg. Med. Chem. Lett. , vol.12 , pp. 307-310
    • Mewshaw, R.1    Meagher, K.2    Zhou, P.3    Zhou, D.4    Shi, X.5    Scerni, R.6    Smith, D.7    Schechter, L.8    Andree, T.9
  • 45
    • 3142579793 scopus 로고    scopus 로고
    • Studies toward the discovery of the next generation of antidepressants. 3. Dual 5-HT1A and serotonin transporter affinity within a class of N-aryloxyethylindolylalkylamines
    • Mewshaw, R.; Zhou, D.; Zhou, P.; Shi, X.; Hornby, G.; Spangler, T.; Scerni, R.; Smith, D.; Schechter, L.; Andree, T. Studies toward the discovery of the next generation of antidepressants. 3. Dual 5-HT1A and serotonin transporter affinity within a class of N-aryloxyethylindolylalkylamines. J. Med. Chem. 2004, 47, 3823-3842.
    • (2004) J. Med. Chem. , vol.47 , pp. 3823-3842
    • Mewshaw, R.1    Zhou, D.2    Zhou, P.3    Shi, X.4    Hornby, G.5    Spangler, T.6    Scerni, R.7    Smith, D.8    Schechter, L.9    Andree, T.10
  • 48
    • 0022892304 scopus 로고
    • Serotonin (5-HT) enhances hippocampal noradrenaline (NA) release: Evidence for facilitatory 5-HT receptors within the CNS
    • Feuerstein, T. H.; Hertting, G. Serotonin (5-HT) enhances hippocampal noradrenaline (NA) release: Evidence for facilitatory 5-HT receptors within the CNS. Naunyn-Schmiedeberg's Arch. Pharmacol. 1986, 333, 191-197.
    • (1986) Naunyn-Schmiedeberg's Arch. Pharmacol. , vol.333 , pp. 191-197
    • Feuerstein, T.H.1    Hertting, G.2
  • 50
    • 0028863081 scopus 로고
    • Synthesis and pharmacological characterization of A-80426: A putative novel antidepressant combining alpha-2 antagonism with 5-HT uptake inhibition
    • Meyer, M.; Hancock, A.; Tietje, K.; Sippy, K.; Giardina, W.; Kerwin, J. Synthesis and pharmacological characterization of A-80426: A putative novel antidepressant combining alpha-2 antagonism with 5-HT uptake inhibition. Bioorg. Med. Chem. Lett. 1995, 5, 2287-2292.
    • (1995) Bioorg. Med. Chem. Lett. , vol.5 , pp. 2287-2292
    • Meyer, M.1    Hancock, A.2    Tietje, K.3    Sippy, K.4    Giardina, W.5    Kerwin, J.6
  • 53
    • 0023850460 scopus 로고
    • Pharmacology of risperidone (R 64 766), a new antipsychotic with serotonin-S2 and dopamine-D2 antagonistic properties
    • 2 activity was risperidone: Janssen, P. A.; Niemegeers, C. J.; Awouters, F.; Schellekens, K. H.; Megens, A. A.; Meert, T. F. Pharmacology of risperidone (R 64 766), a new antipsychotic with serotonin-S2 and dopamine-D2 antagonistic properties. J. Pharmacol. Exp. Ther. 1988, 244, 685-693.
    • (1988) J. Pharmacol. Exp. Ther. , vol.244 , pp. 685-693
    • Janssen, P.A.1    Niemegeers, C.J.2    Awouters, F.3    Schellekens, K.H.4    Megens, A.A.5    Meert, T.F.6
  • 54
    • 0031614543 scopus 로고    scopus 로고
    • Quetiapine: A new atypical antipsychotic for the treatment of schizophrenia
    • Gray, R. Quetiapine: a new atypical antipsychotic for the treatment of schizophrenia. Ment. Health Care 1998, 1, 163-164.
    • (1998) Ment. Health Care , vol.1 , pp. 163-164
    • Gray, R.1
  • 55
    • 0026651080 scopus 로고
    • Neuroendocrine evidence for antagonism of serotonin and dopamine receptors by olanzapine (LY170053), an antipsychotic drug candidate
    • Fuller, R. W.; Snoddy, H. D. Neuroendocrine evidence for antagonism of serotonin and dopamine receptors by olanzapine (LY170053), an antipsychotic drug candidate. Res. Commun. Chem. Pathol. Pharmacol. 1992, 77, 87-93.
    • (1992) Res. Commun. Chem. Pathol. Pharmacol. , vol.77 , pp. 87-93
    • Fuller, R.W.1    Snoddy, H.D.2
  • 60
    • 0020425747 scopus 로고
    • Histamine antagonists and asthma
    • Eiser, N. Histamine antagonists and asthma. Pharmacol. Ther. 1982, 17, 239-250.
    • (1982) Pharmacol. Ther. , vol.17 , pp. 239-250
    • Eiser, N.1
  • 61
    • 0030944646 scopus 로고    scopus 로고
    • Combined antagonism of leukotrienes and histamine produces predominant inhibition of allergen-induced early and late phase airway obstruction in asthmatics
    • Roquet, A.; Dahlen, B.; Kumlin, M.; Ihre, E.; Gudrun, A.; S. Binks, S. Combined antagonism of leukotrienes and histamine produces predominant inhibition of allergen-induced early and late phase airway obstruction in asthmatics. Am. J. Respir. Crit. Care Med. 1997, 155, 1856.
    • (1997) Am. J. Respir. Crit. Care Med. , vol.155 , pp. 1856
    • Roquet, A.1    Dahlen, B.2    Kumlin, M.3    Ihre, E.4    Gudrun, A.5    Binks, S.S.6
  • 66
    • 0026063683 scopus 로고
    • Dual antagonists of platelet-activating factor and histamine. Identification of structural requirements for dual activity of N-acyl-4-(5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene) piperidines
    • Piwinski, J.; Wong, J.; Green, M.; Ganguly, A.; Billah, M.; West, R.; Kreutner, W. Dual antagonists of platelet-activating factor and histamine. Identification of structural requirements for dual activity of N-acyl-4-(5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene) piperidines. J. Med. Chem. 1991, 34, 457-461.
    • (1991) J. Med. Chem. , vol.34 , pp. 457-461
    • Piwinski, J.1    Wong, J.2    Green, M.3    Ganguly, A.4    Billah, M.5    West, R.6    Kreutner, W.7
  • 67
  • 71
    • 0027180453 scopus 로고
    • Application of conformationally restricted Phe-Leu dipeptide mimetic to the design of a combined inhibitor of angiotensinI converting enzyme and neutral endopeptidase 24.11
    • Flynn, G. A.; Beight, D. W.; Mehdi, S.; Koehl, J. R.; Giroux, E. L.; French, J. F.; Hake, P. W.; Dage, R. C. Application of conformationally restricted Phe-Leu dipeptide mimetic to the design of a combined inhibitor of angiotensinI converting enzyme and neutral endopeptidase 24.11. J. Med. Chem. 1993, 36, 2420-2430.
    • (1993) J. Med. Chem. , vol.36 , pp. 2420-2430
    • Flynn, G.A.1    Beight, D.W.2    Mehdi, S.3    Koehl, J.R.4    Giroux, E.L.5    French, J.F.6    Hake, P.W.7    Dage, R.C.8
  • 74
    • 0028891914 scopus 로고
    • Hemodynamic effects of losartan and the endothelin antagonist, SB 209670, in conscious, transgenic ((mRen-2)27), hypertensive rats
    • Gardiner, S. M.; March, J. E.; Kemp, P. A.; Mullins, J. J.; Bennett, T. Hemodynamic effects of losartan and the endothelin antagonist, SB 209670, in conscious, transgenic ((mRen-2)27), hypertensive rats. Br. J. Pharmacol. 1995, 116, 2237-2244.
    • (1995) Br. J. Pharmacol. , vol.116 , pp. 2237-2244
    • Gardiner, S.M.1    March, J.E.2    Kemp, P.A.3    Mullins, J.J.4    Bennett, T.5
  • 79
    • 0035246513 scopus 로고    scopus 로고
    • Cyclooxygenase inhibitors-current status and future prospects
    • Dannhard, G.; Kiefer, W. Cyclooxygenase inhibitors-current status and future prospects. Eur. J. Med. Chem. 2001, 36, 109-126.
    • (2001) Eur. J. Med. Chem. , vol.36 , pp. 109-126
    • Dannhard, G.1    Kiefer, W.2
  • 80
    • 0031960403 scopus 로고    scopus 로고
    • Adverse effects of nonsteroidal antiinflammatory drugs on the gastrointestinal system
    • Fosslien, E. Adverse effects of nonsteroidal antiinflammatory drugs on the gastrointestinal system. Ann. Clin. Lab. Sci. 1998, 28, 67-81.
    • (1998) Ann. Clin. Lab. Sci. , vol.28 , pp. 67-81
    • Fosslien, E.1
  • 81
    • 0031667976 scopus 로고    scopus 로고
    • Differential effects of inhibitors of cyclooxygenase (cyclooxygenase 1 and cyclooxygenase 2) in acute inflammation
    • Gilroy, D. W.; Tomlinson, A.; Willoughby, D. A. Differential effects of inhibitors of cyclooxygenase (cyclooxygenase 1 and cyclooxygenase 2) in acute inflammation. Eur. J. Pharmacol. 1998, 355, 211-217.
    • (1998) Eur. J. Pharmacol. , vol.355 , pp. 211-217
    • Gilroy, D.W.1    Tomlinson, A.2    Willoughby, D.A.3
  • 82
    • 0035584272 scopus 로고    scopus 로고
    • Dual inhibitors of COX and 5-LOX. A new avenue in anti-inflammatory therapy
    • Fiorucci, S.; Meli, R.; Bucci, M.; Cirino, G. Dual inhibitors of COX and 5-LOX. A new avenue in anti-inflammatory therapy. Biochem. Pharmacol. 2001, 62, 1433-1438.
    • (2001) Biochem. Pharmacol. , vol.62 , pp. 1433-1438
    • Fiorucci, S.1    Meli, R.2    Bucci, M.3    Cirino, G.4
  • 84
    • 0042574211 scopus 로고    scopus 로고
    • Dual inhibition of COX-2 and 5-LOX as a new strategy to provide safer non-steroidal anti-inflammatory drugs
    • Charlier, C.; Michaux, C. Dual inhibition of COX-2 and 5-LOX as a new strategy to provide safer non-steroidal anti-inflammatory drugs. Eur. J. Med. Chem. 2003, 38, 645-659.
    • (2003) Eur. J. Med. Chem. , vol.38 , pp. 645-659
    • Charlier, C.1    Michaux, C.2
  • 85
    • 0020285864 scopus 로고
    • 2,6-Di-tert-4(2′-thenoyl)phenol-(R-830): A novel nonsteroidal anti-inflammatory agent with antioxidant properties
    • Swingle, K. F.; Moore, G. G. I. 2,6-Di-tert-4(2′-thenoyl)phenol-(R- 830): A novel nonsteroidal anti-inflammatory agent with antioxidant properties. Agents Actions 1982, 12, 674-683.
    • (1982) Agents Actions , vol.12 , pp. 674-683
    • Swingle, K.F.1    Moore, G.G.I.2
  • 87
    • 0028031723 scopus 로고
    • Synthesis and biological evaluation of 5-[[3,5-bis(1,1-dimethyl)-4- hydroxyphenyl]methylene]oxazoles, -thiazoles, and -imidazoles: Novel dual 5-LOX and COX inhibitors with anti-inflamatory activity
    • Unangst, P. C.; Connor, D. T.; Cetenko, W. A.; Sorenson, R. J.; Kostlan, C. R.; Sircar, J. C.; Wright, C. D.; Schrier, D. J.; Dyer, R. D. Synthesis and biological evaluation of 5-[[3,5-bis(1,1-dimethyl)-4-hydroxyphenyl]methylene] oxazoles, -thiazoles, and -imidazoles: Novel dual 5-LOX and COX inhibitors with anti-inflamatory activity. J. Med. Chem. 1994, 37, 322-328.
    • (1994) J. Med. Chem. , vol.37 , pp. 322-328
    • Unangst, P.C.1    Connor, D.T.2    Cetenko, W.A.3    Sorenson, R.J.4    Kostlan, C.R.5    Sircar, J.C.6    Wright, C.D.7    Schrier, D.J.8    Dyer, R.D.9
  • 92
    • 0028289770 scopus 로고
    • (6,7-Diarylhydropyrrolizin-5-yl)acetic acids, a novel class of potent dual inhibitors of both cyclooxygenase and 5-lipoxygenase
    • Laufer, S. A.; Augustin, J.; Dannhardt, G.; Kiefer, W. (6,7-Diarylhydropyrrolizin-5-yl)acetic acids, a novel class of potent dual inhibitors of both cyclooxygenase and 5-lipoxygenase. J. Med. Chem. 1994, 37, 1894-1897.
    • (1994) J. Med. Chem. , vol.37 , pp. 1894-1897
    • Laufer, S.A.1    Augustin, J.2    Dannhardt, G.3    Kiefer, W.4
  • 94
    • 0022337224 scopus 로고
    • The biochemical pharmacology of thromboxane synthase inhibition in man
    • Fitzgerald, G. A.; Reilly, I. A. G.; Pederson, A. K. The biochemical pharmacology of thromboxane synthase inhibition in man. Circulation 1985, 72, 1194-1201.
    • (1985) Circulation , vol.72 , pp. 1194-1201
    • Fitzgerald, G.A.1    Reilly, I.A.G.2    Pederson, A.K.3
  • 95
    • 0021773158 scopus 로고
    • Thromboxane synthase inhibition combined with thromboxane receptor blockade: A step forward in antithrombotic strategy?
    • Gresele, P.; van Houte, E.; Arnout, J.; Deckmyn, H.; Vermylen, J. Thromboxane synthase inhibition combined with thromboxane receptor blockade: a step forward in antithrombotic strategy? Thromb. Haemostasis 1984, 52, 364.
    • (1984) Thromb. Haemostasis , vol.52 , pp. 364
    • Gresele, P.1    Van Houte, E.2    Arnout, J.3    Deckmyn, H.4    Vermylen, J.5
  • 96
    • 0024559585 scopus 로고
    • R 68 070: Thromboxane A2 synthetase inhibition and thromboxane A2/prostaglandin endoperoxide receptor blockade combined in one molecule. II. Pharmacological effects in vivo and ex vivo
    • De Clerck, F.; Beetens, J.; Van de Water, A.; Vercammen, E.; Janssen, P. A. R 68 070: thromboxane A2 synthetase inhibition and thromboxane A2/prostaglandin endoperoxide receptor blockade combined in one molecule. II. Pharmacological effects in vivo and ex vivo. Thromb. Haemostasis 1989, 61, 43-49.
    • (1989) Thromb. Haemostasis , vol.61 , pp. 43-49
    • De Clerck, F.1    Beetens, J.2    Van De Water, A.3    Vercammen, E.4    Janssen, P.A.5
  • 97
    • 0021909254 scopus 로고
    • Thromboxane synthetase inhibitors (TXSI). Design, synthesis, and evaluation of a novel series of ω-pyridylalkenoic acids
    • Kato, K.; Ohkawa, S.; Terao, S.; Terashita, Z. I.; Nishikava, K. Thromboxane synthetase inhibitors (TXSI). Design, synthesis, and evaluation of a novel series of ω-pyridylalkenoic acids. J. Med. Chem. 1985, 28, 287-294.
    • (1985) J. Med. Chem. , vol.28 , pp. 287-294
    • Kato, K.1    Ohkawa, S.2    Terao, S.3    Terashita, Z.I.4    Nishikava, K.5
  • 98
    • 0027958114 scopus 로고
    • 6,6-Disubstituted hex-5-enoic acid derivatives as combined thromboxane A2 receptor and synthetase inhibitors
    • Soyka, R.; Heckel, A.; Nickl, J.; Eisert, W.; Muller, T. H.; Weisenberger, H. 6,6-Disubstituted hex-5-enoic acid derivatives as combined thromboxane A2 receptor and synthetase inhibitors. J. Med. Chem. 1994, 37, 26-39.
    • (1994) J. Med. Chem. , vol.37 , pp. 26-39
    • Soyka, R.1    Heckel, A.2    Nickl, J.3    Eisert, W.4    Muller, T.H.5    Weisenberger, H.6
  • 99
    • 0028847158 scopus 로고
    • Tromboxane modulating agents. 1. Design of 1-[(arylsulfonyl)amino] alkylindole derivatives as dual thromboxane synthase inhibitor/thromboxane receptor antagonist
    • Dickinson, R. P.; Dack, K. N.; Steele, J. Tromboxane modulating agents. 1. Design of 1-[(arylsulfonyl)amino] alkylindole derivatives as dual thromboxane synthase inhibitor/thromboxane receptor antagonist. Bioorg. Med. Chem. Lett. 1995, 5, 3017-3022.
    • (1995) Bioorg. Med. Chem. Lett. , vol.5 , pp. 3017-3022
    • Dickinson, R.P.1    Dack, K.N.2    Steele, J.3
  • 100
    • 3843079807 scopus 로고    scopus 로고
    • Peroxisome proliferator-activated receptor α/γ dual agonists for the treatment of type 2 diabetes
    • Henke, B. Peroxisome proliferator-activated receptor α/γ dual agonists for the treatment of type 2 diabetes. J. Med. Chem. 2004, 47, 4118-4127.
    • (2004) J. Med. Chem. , vol.47 , pp. 4118-4127
    • Henke, B.1
  • 103
    • 18744385217 scopus 로고    scopus 로고
    • Design and synthesis of novel PPARα/γ/δ triple activators using known PPARα/γ dual activator as structural template
    • Mogensen, J. P.; Jeppesen, L.; Bury, P. S. Design and synthesis of novel PPARα/γ/δ triple activators using known PPARα/γ dual activator as structural template. Bioorg. Med. Chem. Lett. 2003, 13, 257-260.
    • (2003) Bioorg. Med. Chem. Lett. , vol.13 , pp. 257-260
    • Mogensen, J.P.1    Jeppesen, L.2    Bury, P.S.3
  • 105
    • 0031024171 scopus 로고    scopus 로고
    • Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
    • Lipinski, C. A.; Lombardo, F.; Dominy, B. W.; Feeney, P. J. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Adv. Drug Delivery Rev. 1997, 23, 3-25.
    • (1997) Adv. Drug Delivery Rev. , vol.23 , pp. 3-25
    • Lipinski, C.A.1    Lombardo, F.2    Dominy, B.W.3    Feeney, P.J.4
  • 106
    • 0037030653 scopus 로고    scopus 로고
    • Molecular properties that influence the oral bioavailability of drug candidates
    • Veber, D. F.; Johnson, S. R.; Cheng, H. Y.; Smith, B. R.; Ward, K. W.; Kopple, K. D. Molecular properties that influence the oral bioavailability of drug candidates. J. Med. Chem. 2002, 45, 2615-2623.
    • (2002) J. Med. Chem. , vol.45 , pp. 2615-2623
    • Veber, D.F.1    Johnson, S.R.2    Cheng, H.Y.3    Smith, B.R.4    Ward, K.W.5    Kopple, K.D.6
  • 108
    • 1642540579 scopus 로고    scopus 로고
    • Unexpected nanomolar inhibition of carbonic anhydrase by COX-2-selective celecoxib: New pharmacological opportunities due to related binding site recognition
    • Weber, A.; Casini, A.; Heine, A.; Kuhn, D.; Supuran, C. T.; Scozzafava, A.; Klebe, G. Unexpected nanomolar inhibition of carbonic anhydrase by COX-2-selective celecoxib: New pharmacological opportunities due to related binding site recognition. J. Med. Chem. 2003, 46, 550-557.
    • (2003) J. Med. Chem. , vol.46 , pp. 550-557
    • Weber, A.1    Casini, A.2    Heine, A.3    Kuhn, D.4    Supuran, C.T.5    Scozzafava, A.6    Klebe, G.7


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