메뉴 건너뛰기




Volumn 9, Issue 15, 2004, Pages 641-651

From magic bullets to designed multiple ligands

Author keywords

Chemical Biology; conjugate; Designed; Drug Discovery; guidelines; ligand; multiple; overlap; Pharmaceutical Science; pharmacophore; superfamily

Indexed keywords

5 HYDROXYTRYPTAMINE 2A RECEPTOR ANTAGONIST; 6 [[3 FLUORO 5 (3,4,5,6 TETRAHYDRO 4 METHOXY 2H PYRAN 4 YL)]PHENOXYMETHYL] 1 METHYL 2 QUINOLONE; ACETYLSALICYLIC ACID; ACETYLSALICYLIC ACID 3 (NITROXYMETHYL)PHENYL ESTER; AMITRIPTYLINE; ANTIDEPRESSANT AGENT; ANTIHYPERTENSIVE AGENT; ANTIINFLAMMATORY AGENT; CELECOXIB; CHOLINESTERASE INHIBITOR; CYCLOOXYGENASE 2 INHIBITOR; DIPEPTIDYL CARBOXYPEPTIDASE INHIBITOR; DOPAMINE D4 RECEPTOR ANTAGONIST; DOPAMINE RECEPTOR BLOCKING AGENT; ENKEPHALINASE INHIBITOR; FLUOXETINE; IBUPROFEN DERIVATIVE; IRBESARTAN; LIPOXYGENASE INHIBITOR; NETOGLITAZONE; NEUROLEPTIC AGENT; NORADRENALIN TRANSPORTER; OMAPATRILAT; PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR AGONIST; RIDOGREL; SEROTONIN ANTAGONIST; SEROTONIN TRANSPORTER; THROMBIN INHIBITOR; THROMBOXANE A2 RECEPTOR BLOCKING AGENT; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 3242794178     PISSN: 13596446     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1359-6446(04)03163-0     Document Type: Review
Times cited : (688)

References (54)
  • 1
    • 0032938106 scopus 로고    scopus 로고
    • Omapatrilat
    • Graul A., et al. Omapatrilat. Drugs Future. 24:1999;269-277
    • (1999) Drugs Future , vol.24 , pp. 269-277
    • Graul, A.1
  • 2
    • 0036254257 scopus 로고    scopus 로고
    • Netoglitazone
    • Sorbera L.A., et al. Netoglitazone. Drugs Future. 27:2002;132-139
    • (2002) Drugs Future , vol.27 , pp. 132-139
    • Sorbera, L.A.1
  • 3
    • 0037060906 scopus 로고    scopus 로고
    • Synthesis and activity of a new methoxytetrahydropyran derivative as dual cyclooxygenase-2/5-lipoxygenase inhibitor
    • Barbey S., et al. Synthesis and activity of a new methoxytetrahydropyran derivative as dual cyclooxygenase-2/5-lipoxygenase inhibitor. Bioorg. Med. Chem. Lett. 12:2002;779-782
    • (2002) Bioorg. Med. Chem. Lett. , vol.12 , pp. 779-782
    • Barbey, S.1
  • 4
    • 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. 54:1997;567-572
    • (1997) Arch. Gen. Psychiatry , vol.54 , pp. 567-572
    • Kramer, M.S.1
  • 5
    • 9144232388 scopus 로고    scopus 로고
    • Pyrrolo[1,3]benzothiazepine-based serotonin and dopamine receptor antagonists. Molecular modeling, further structure-activity relationship studies, and identification of novel atypical antipsychotic agents
    • Campiani G., et al. Pyrrolo[1,3]benzothiazepine-based serotonin and dopamine receptor antagonists. Molecular modeling, further structure-activity relationship studies, and identification of novel atypical antipsychotic agents. J. Med. Chem. 47:2004;143-157
    • (2004) J. Med. Chem. , vol.47 , pp. 143-157
    • Campiani, G.1
  • 6
    • 0036283366 scopus 로고    scopus 로고
    • New targets for antipsychotics
    • Jones H.M., et al. New targets for antipsychotics. Expert Rev. Neurother. 2:2002;61-68
    • (2002) Expert Rev. Neurother. , vol.2 , pp. 61-68
    • Jones, H.M.1
  • 7
    • 0037115290 scopus 로고    scopus 로고
    • Comparative efficacy between venlafaxine and SSRIs: A pooled analysis of patients with depression
    • Stahl S.M., et al. Comparative efficacy between venlafaxine and SSRIs: a pooled analysis of patients with depression. Biol. Psychiatry. 52:2002;1166-1174
    • (2002) Biol. Psychiatry , vol.52 , pp. 1166-1174
    • Stahl, S.M.1
  • 9
    • 0035846069 scopus 로고    scopus 로고
    • A new class of ibuprofen derivatives with reduced gastrotoxicity
    • Gasco A., et al. A new class of ibuprofen derivatives with reduced gastrotoxicity. J. Med. Chem. 44:2001;3463-3468
    • (2001) J. Med. Chem. , vol.44 , pp. 3463-3468
    • Gasco, A.1
  • 10
    • 0026659612 scopus 로고
    • 'Mixed Inhibitor-Prodrug' as a new approach toward systemically active inhibitors of enkephalin-degrading enzymes
    • Roques B.P., et al. 'Mixed Inhibitor-Prodrug' as a new approach toward systemically active inhibitors of enkephalin-degrading enzymes. J. Med. Chem. 35:1992;2473-2481
    • (1992) J. Med. Chem. , vol.35 , pp. 2473-2481
    • Roques, B.P.1
  • 11
    • 0033584213 scopus 로고    scopus 로고
    • Design and synthesis of a novel synthetic NAPAP-pentasaccharide conjugate displaying a dual antithrombotic action
    • Buijsman R.C., et al. Design and synthesis of a novel synthetic NAPAP-pentasaccharide conjugate displaying a dual antithrombotic action. Bioorg. Med. Chem. Lett. 9:1999;2013-2018
    • (1999) Bioorg. Med. Chem. Lett. , vol.9 , pp. 2013-2018
    • Buijsman, R.C.1
  • 12
    • 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. 44:2001;2259-2269
    • (2001) J. Med. Chem. , vol.44 , pp. 2259-2269
    • Portoghese, P.S.1
  • 13
    • 0037194633 scopus 로고    scopus 로고
    • Discovery of N-isoxazolyl biphenylsulfonamides as potent dual angiotensin I and endothelin a receptor antagonists
    • Murugesan N., et al. Discovery of N-isoxazolyl biphenylsulfonamides as potent dual angiotensin I and endothelin A receptor antagonists. J. Med. Chem. 45:2002;3829-3835
    • (2002) J. Med. Chem. , vol.45 , pp. 3829-3835
    • Murugesan, N.1
  • 15
    • 0030697345 scopus 로고    scopus 로고
    • 1 receptor antagonist activity
    • 1 receptor antagonist activity. Bioorg. Med. Chem. Lett. 7:1997;2825-2830
    • (1997) Bioorg. Med. Chem. Lett. , vol.7 , pp. 2825-2830
    • Vaz, R.J.1
  • 16
    • 0030899302 scopus 로고    scopus 로고
    • Rupatadine, a new potent, orally active dual antagonist of histamine and platelet activating factor (PAF)
    • Merlos M., et al. Rupatadine, a new potent, orally active dual antagonist of histamine and platelet activating factor (PAF). J. Pharmacol. Exp. Ther. 280:1997;114-121
    • (1997) J. Pharmacol. Exp. Ther. , vol.280 , pp. 114-121
    • Merlos, M.1
  • 17
    • 0037025455 scopus 로고    scopus 로고
    • N-[2-indan-1-yl)-3-mercapto-propionyl] amino acids as highly potent inhibitors of the three vasopeptidases (NEP, ACE, ECE): In vitro and in vivo activities
    • Roques B.P., et al. N-[2-indan-1-yl)-3-mercapto-propionyl] amino acids as highly potent inhibitors of the three vasopeptidases (NEP, ACE, ECE): in vitro and in vivo activities. Bioorg. Med. Chem. Lett. 12:2002;2001-2005
    • (2002) Bioorg. Med. Chem. Lett. , vol.12 , pp. 2001-2005
    • Roques, B.P.1
  • 18
    • 10744225421 scopus 로고    scopus 로고
    • Synthesis and biological activity of piperazine-based dual MMP-13 and TNF-α converting enzyme inhibitors
    • Letavic M.A., et al. Synthesis and biological activity of piperazine-based dual MMP-13 and TNF-α converting enzyme inhibitors. Bioorg. Med. Chem. Lett. 13:2003;3243-3246
    • (2003) Bioorg. Med. Chem. Lett. , vol.13 , pp. 3243-3246
    • Letavic, M.A.1
  • 19
    • 0034883069 scopus 로고    scopus 로고
    • Inhibition of tumor necrosis factor-alpha (TNF-α) production and arthritis in the rat by GW3333, a dual inhibitor of TNF-α-converting enzyme and matrix metalloproteinases
    • Conway J.G., et al. Inhibition of tumor necrosis factor-alpha (TNF-α) production and arthritis in the rat by GW3333, a dual inhibitor of TNF-α-converting enzyme and matrix metalloproteinases. J. Pharmacol. Exp. Ther. 298:2001;900-908
    • (2001) J. Pharmacol. Exp. Ther. , vol.298 , pp. 900-908
    • Conway, J.G.1
  • 20
    • 0037059929 scopus 로고    scopus 로고
    • Design and synthesis of dual inhibitor for matrix metalloproteinase and cathepsin
    • Ikeda S., et al. Design and synthesis of dual inhibitor for matrix metalloproteinase and cathepsin. Bioorg. Med. Chem. Lett. 12:2002;375-378
    • (2002) Bioorg. Med. Chem. Lett. , vol.12 , pp. 375-378
    • Ikeda, S.1
  • 21
    • 12444346791 scopus 로고    scopus 로고
    • A conformational restriction approach to the development of dual inhibitors of acetylcholinesterase and serotonin transporter as potential agents for Alzheimer's disease
    • Kogen H., et al. A conformational restriction approach to the development of dual inhibitors of acetylcholinesterase and serotonin transporter as potential agents for Alzheimer's disease. Bioorg. Med. Chem. 11:2003;4389-4415
    • (2003) Bioorg. Med. Chem. , vol.11 , pp. 4389-4415
    • Kogen, H.1
  • 22
    • 0028847158 scopus 로고
    • Thromboxane modulating agents. 1. Design of 1-[(arylsulfonyl)amino] alkylindole derivatives as dual thromboxane synthase inhibitor/thromboxane receptor antagonists
    • Dickinson R.P., et al. Thromboxane modulating agents. 1. Design of 1-[(arylsulfonyl)amino] alkylindole derivatives as dual thromboxane synthase inhibitor/thromboxane receptor antagonists. Bioorg. Med. Chem. Lett. 5:1995;3017-3022
    • (1995) Bioorg. Med. Chem. Lett. , vol.5 , pp. 3017-3022
    • Dickinson, R.P.1
  • 23
    • 0037059946 scopus 로고    scopus 로고
    • Approach to dual-acting platelet activating factor (PAF) receptor antagonist/thromboxane synthase inhibitor (TxSI) based on the link of PAF antagonist and TxSIs
    • Fujita M., et al. Approach to dual-acting platelet activating factor (PAF) receptor antagonist/thromboxane synthase inhibitor (TxSI) based on the link of PAF antagonist and TxSIs. Bioorg. Med. Chem. Lett. 12:2002;341-344
    • (2002) Bioorg. Med. Chem. Lett. , vol.12 , pp. 341-344
    • Fujita, M.1
  • 24
    • 18244364895 scopus 로고    scopus 로고
    • 1 antagonists-serotonin reuptake inhibitors: Synthesis and SAR of a new class of potential antidepressants
    • 1 antagonists-serotonin reuptake inhibitors: synthesis and SAR of a new class of potential antidepressants. Bioorg. Med. Chem. Lett. 12:2002;261-264
    • (2002) Bioorg. Med. Chem. Lett. , vol.12 , pp. 261-264
    • Ryckmans, T.1
  • 25
    • 18244424424 scopus 로고
    • Potent dual antagonist of endothelin and angiotensin II receptors derived from alpha-phenoxyphenylacetic acids (Part III)
    • Walsh T.F., et al. Potent dual antagonist of endothelin and angiotensin II receptors derived from alpha-phenoxyphenylacetic acids (Part III). Bioorg. Med. Chem. Lett. 5:1995;1155-1158
    • (1995) Bioorg. Med. Chem. Lett. , vol.5 , pp. 1155-1158
    • Walsh, T.F.1
  • 26
    • 0035914604 scopus 로고    scopus 로고
    • Identification of a series of PPARγ/δ dual agonists via solid-phase parallel synthesis
    • Sternbach D., et al. Identification of a series of PPARγ/δ dual agonists via solid-phase parallel synthesis. Bioorg. Med. Chem. Lett. 11:2001;2959-2962
    • (2001) Bioorg. Med. Chem. Lett. , vol.11 , pp. 2959-2962
    • Sternbach, D.1
  • 27
    • 1542268206 scopus 로고    scopus 로고
    • Selective optimization of side activities: Another way for drug discovery
    • Wermuth C.G. Selective optimization of side activities: another way for drug discovery. J. Med. Chem. 47:2004;1303-1314
    • (2004) J. Med. Chem. , vol.47 , pp. 1303-1314
    • Wermuth, C.G.1
  • 28
    • 0035847383 scopus 로고    scopus 로고
    • 3 antagonist tropisetron (ICS 205-930) is a potent and selective α7 nicotinic receptor partial agonist
    • 3 antagonist tropisetron (ICS 205-930) is a potent and selective α7 nicotinic receptor partial agonist. Bioorg. Med. Chem. Lett. 11:2001;319-321
    • (2001) Bioorg. Med. Chem. Lett. , vol.11 , pp. 319-321
    • MacOr, J.E.1
  • 29
    • 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., et al. Unexpected nanomolar inhibition of carbonic anhydrase by COX-2-selective celecoxib: new pharmacological opportunities due to related binding site recognition. J. Med. Chem. 46:2003;550-557
    • (2003) J. Med. Chem. , vol.46 , pp. 550-557
    • Weber, A.1
  • 30
    • 0344927047 scopus 로고    scopus 로고
    • Duloxetine (Cymbaltaô), as dual inhibitor of serotonin and norepinephrine reuptake
    • Gallagher P.T., et al. Duloxetine (Cymbaltaô), as dual inhibitor of serotonin and norepinephrine reuptake. Bioorg. Med. Chem. Lett. 13:2003;4477-4480
    • (2003) Bioorg. Med. Chem. Lett. , vol.13 , pp. 4477-4480
    • Gallagher, P.T.1
  • 31
    • 0037020743 scopus 로고    scopus 로고
    • 4 receptor antagonists. Part 2. Asymmetric synthesis and biological evaluation
    • 4 receptor antagonists. Part 2. Asymmetric synthesis and biological evaluation. Bioorg. Med. Chem. Lett. 12:2002;3111-3115
    • (2002) Bioorg. Med. Chem. Lett. , vol.12 , pp. 3111-3115
    • Zhao, H.1
  • 32
    • 0037186501 scopus 로고    scopus 로고
    • 3 receptor ligands with combined inhibitory histamine N-methyl transferase activity
    • 3 receptor ligands with combined inhibitory histamine N-methyl transferase activity. J. Med. Chem. 45:2002;1128-1141
    • (2002) J. Med. Chem. , vol.45 , pp. 1128-1141
    • Stark, H.1
  • 33
    • 0032480820 scopus 로고    scopus 로고
    • 2-adrenoreceptor agonists for the treatment of airway diseases. 1. Discovery and biological evaluation of some 7-(2-aminoethyl)-4-hydroxybenzothiazol-2(3H)-one analogues
    • 2- adrenoreceptor agonists for the treatment of airway diseases. 1. Discovery and biological evaluation of some 7-(2-aminoethyl)-4-hydroxybenzothiazol-2(3H)-one analogues. J. Med. Chem. 41:1998;4915-4917
    • (1998) J. Med. Chem. , vol.41 , pp. 4915-4917
    • Ince, F.1
  • 34
    • 0030576290 scopus 로고    scopus 로고
    • 2 and gastrin receptor antagonists
    • 2 and gastrin receptor antagonists. Bioorg. Med. Chem. Lett. 6:1996;1421-1426
    • (1996) Bioorg. Med. Chem. Lett. , vol.6 , pp. 1421-1426
    • Hagishita, Y.1
  • 35
    • 12444300117 scopus 로고    scopus 로고
    • Macrocyclic bisindolemaleimides as inhibitors of protein kinase C and glycogen synthase kinase-3
    • Zhang H-C., et al. Macrocyclic bisindolemaleimides as inhibitors of protein kinase C and glycogen synthase kinase-3. Bioorg. Med. Chem. Lett. 13:2003;3049-3053
    • (2003) Bioorg. Med. Chem. Lett. , vol.13 , pp. 3049-3053
    • Zhang, H.-C.1
  • 36
    • 0031024171 scopus 로고    scopus 로고
    • Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
    • Lipinski C.A., et al. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Adv. Drug Deliv. Rev. 23:1997;3-25
    • (1997) Adv. Drug Deliv. Rev. , vol.23 , pp. 3-25
    • Lipinski, C.A.1
  • 37
    • 0037030653 scopus 로고    scopus 로고
    • Molecular properties that influence the oral bioavailability of drug candidates
    • Veber D.F., et al. Molecular properties that influence the oral bioavailability of drug candidates. J. Med. Chem. 45:2002;2615-2623
    • (2002) J. Med. Chem. , vol.45 , pp. 2615-2623
    • Veber, D.F.1
  • 38
    • 0035438391 scopus 로고    scopus 로고
    • Is there a difference between leads and drugs? a historical perspective
    • Oprea T.I., et al. Is there a difference between leads and drugs? A historical perspective. J. Chem. Inf. Comput. Sci. 41:2001;1308-1315
    • (2001) J. Chem. Inf. Comput. Sci. , vol.41 , pp. 1308-1315
    • Oprea, T.I.1
  • 39
    • 0037020768 scopus 로고    scopus 로고
    • 2 binding activities of a series of diacyl-substituted 2-arylpiperazines
    • 2 binding activities of a series of diacyl-substituted 2-arylpiperazines. Bioorg. Med. Chem. Lett. 12:2002;3161-3165
    • (2002) Bioorg. Med. Chem. Lett. , vol.12 , pp. 3161-3165
    • Blythin, D.J.1
  • 41
    • 0030882035 scopus 로고    scopus 로고
    • Actions of tramadol, its enantiomers and principal metabolite, O-desmethyltramadol, on serotonin efflux and uptake
    • Bamigbade T.A., et al. Actions of tramadol, its enantiomers and principal metabolite, O-desmethyltramadol, on serotonin efflux and uptake. Br. J. Anaesth. 79:1997;352-356
    • (1997) Br. J. Anaesth. , vol.79 , pp. 352-356
    • Bamigbade, T.A.1
  • 42
    • 0028240168 scopus 로고
    • Dual angiotensin converting enzyme/thromboxane synthase inhibitors
    • Ksander G.M., et al. Dual angiotensin converting enzyme/thromboxane synthase inhibitors. J. Med. Chem. 37:1994;1823-1832
    • (1994) J. Med. Chem. , vol.37 , pp. 1823-1832
    • Ksander, G.M.1
  • 43
    • 0029761095 scopus 로고    scopus 로고
    • 2 synthase inhibitory activities
    • 2 synthase inhibitory activities. Chem. Pharm. Bull. (Tokyo). 44:1996;1510-1520
    • (1996) Chem. Pharm. Bull. (Tokyo) , vol.44 , pp. 1510-1520
    • Sakurai, S.1
  • 44
    • 0345550537 scopus 로고    scopus 로고
    • DPI-3290 [(+)-3-((alpha-R)-alpha-((2S,5R)-4-Allyl-2,5-dimethyl-1- piperazinyl)-3-hydroxybenzyl)-N-(3-fluorophenyl)-N-methylbenzamide]. I. Mixed opioid agonist with potent antinociceptive activity
    • Gengo P.J., et al. DPI-3290 [(+)-3-((alpha-R)-alpha-((2S,5R)-4-Allyl-2,5- dimethyl-1-piperazinyl)-3-hydroxybenzyl)-N-(3-fluorophenyl)-N-methylbenzamide]. I. Mixed opioid agonist with potent antinociceptive activity. J. Pharmacol. Exp. Ther. 307:2003;1221-1226
    • (2003) J. Pharmacol. Exp. Ther. , vol.307 , pp. 1221-1226
    • Gengo, P.J.1
  • 45
    • 85056014891 scopus 로고    scopus 로고
    • Toward an optimal joint recognition of the S1′ subsites of ECE-1, ACE, and NEP
    • Roques B-P., et al. Toward an optimal joint recognition of the S1′ subsites of ECE-1, ACE, and NEP. J. Med. Chem. 45:2002;1477-1486
    • (2002) J. Med. Chem. , vol.45 , pp. 1477-1486
    • Roques, B.-P.1
  • 46
    • 10744233215 scopus 로고    scopus 로고
    • Bicyclo[2.2.1]heptanes as novel triple re-uptake inhibitors for the treatment of depression
    • Martin F.M., et al. Bicyclo[2.2.1]heptanes as novel triple re-uptake inhibitors for the treatment of depression. Bioorg. Med. Chem. Lett. 13:2003;3277-3280
    • (2003) Bioorg. Med. Chem. Lett. , vol.13 , pp. 3277-3280
    • Martin, F.M.1
  • 47
    • 0034675695 scopus 로고    scopus 로고
    • The design and synthesis of novel NK1/NK2 dual antagonists
    • Reichard G.A., et al. The design and synthesis of novel NK1/NK2 dual antagonists. Bioorg. Med. Chem. Lett. 10:2000;2329-2332
    • (2000) Bioorg. Med. Chem. Lett. , vol.10 , pp. 2329-2332
    • Reichard, G.A.1
  • 49
    • 0037430564 scopus 로고    scopus 로고
    • Amphipathic 3-phenyl-7-propylbenzisoxazoles; Human PPARγ,δ, α agonists
    • Adams A.D., et al. Amphipathic 3-phenyl-7-propylbenzisoxazoles; human PPARγ,δ,α agonists. Bioorg. Med. Chem. Lett. 13:2003;931-935
    • (2003) Bioorg. Med. Chem. Lett. , vol.13 , pp. 931-935
    • Adams, A.D.1
  • 50
    • 0033539108 scopus 로고    scopus 로고
    • Synthesis, opioid receptor binding, and biological activities of naltrexone-derived pyrido-and pyrimidomorphinans
    • Ananthan S., et al. Synthesis, opioid receptor binding, and biological activities of naltrexone-derived pyrido-and pyrimidomorphinans. J. Med. Chem. 42:1999;3527-3538
    • (1999) J. Med. Chem. , vol.42 , pp. 3527-3538
    • Ananthan, S.1
  • 51
    • 0242299587 scopus 로고    scopus 로고
    • Large dimeric ligands with favorable pharmacokinetic properties and peroxisome proliferator-activated receptor agonist activity in vitro and in vivo
    • Sauerberg P., et al. Large dimeric ligands with favorable pharmacokinetic properties and peroxisome proliferator-activated receptor agonist activity in vitro and in vivo. J. Med. Chem. 46:2003;4883-4894
    • (2003) J. Med. Chem. , vol.46 , pp. 4883-4894
    • Sauerberg, P.1
  • 52
    • 3242804148 scopus 로고    scopus 로고
    • CGS 34226, a thiol-based dual inhibitor of endothelin converting enzyme-1 and neutral endopeptidase
    • Jeng A.Y., et al. CGS 34226, a thiol-based dual inhibitor of endothelin converting enzyme-1 and neutral endopeptidase. Clin. Sci. 103:2002;985-1015
    • (2002) Clin. Sci. , vol.103 , pp. 985-1015
    • Jeng, A.Y.1
  • 53
    • 0028003993 scopus 로고
    • Dual inhibition of neutral endopeptidase and angiotensin-converting enzyme by N-phosphomethyl and N-carboxyalkyl dipeptides
    • De Lombaert S., et al. Dual inhibition of neutral endopeptidase and angiotensin-converting enzyme by N-phosphomethyl and N-carboxyalkyl dipeptides. Bioorg. Med. Chem. Lett. 22:1994;2715-2720
    • (1994) Bioorg. Med. Chem. Lett. , vol.22 , pp. 2715-2720
    • De Lombaert, S.1
  • 54
    • 0038610570 scopus 로고    scopus 로고
    • Systematic discovery of multicomponent therapeutics
    • Borisy A., et al. Systematic discovery of multicomponent therapeutics. Proc. Natl. Acad. Sci. U. S. A. 100:2003;7977-7982
    • (2003) Proc. Natl. Acad. Sci. U. S. A. , vol.100 , pp. 7977-7982
    • Borisy, A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.