메뉴 건너뛰기




Volumn 11, Issue 7-8, 2006, Pages 348-354

Similarity in drugs: reflections on analogue design

Author keywords

[No Author keywords available]

Indexed keywords

3 AMINO 2 (3 CARBOXYPROPYL) 6 (4 METHOXYPHENYL)PYRIDAZINIUM BROMIDE; 9 (2 HYDROXY 3 NONYL)ADENINE; ANTIDEPRESSANT AGENT; ANTIHYPERTENSIVE AGENT; BAZINAPRINE; BENZODIAZEPINE; BMS 192548; CAPTOPRIL; CHLORPROMAZINE; CIMETIDINE; CLOPIMOZIDE; CYCLOOXYGENASE 2 INHIBITOR; DEXAMISOLE; DIAZEPAM; DIPEPTIDYL CARBOXYPEPTIDASE INHIBITOR; DRUG ANALOG; HALOPERIDOL; HISTAMINE H2 RECEPTOR ANTAGONIST; HYDROXYMETHYLGLUTARYL COENZYME A REDUCTASE INHIBITOR; IMIPRAMINE; ISOXAZOLE DERIVATIVE; LEVAMISOLE; MEVINOLIN; MIBEFRADIL; MINAPRINE; NEUROLEPTIC AGENT; PHOSPHODIESTERASE V INHIBITOR; TRANQUILIZER; UNINDEXED DRUG; ZAPRINAST; ZOLPIDEM; ZOPICLONE;

EID: 33645855871     PISSN: 13596446     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.drudis.2006.02.006     Document Type: Review
Times cited : (70)

References (35)
  • 1
    • 33645883209 scopus 로고    scopus 로고
    • Fischer, J. et al. (2005) Analogue-based drug discovery, IUPAC Project 2002-051-0-700
  • 2
    • 84889836103 scopus 로고    scopus 로고
    • Fischer, J. and Ganellin, C.R. (eds) (2006) Analogue-based drug discovery, Wiley-VCH
  • 3
    • 0037124196 scopus 로고    scopus 로고
    • Drugs, leads, and drug-likeness: an analysis of some recently launched drugs
    • Proudfoot J.R. Drugs, leads, and drug-likeness: an analysis of some recently launched drugs. Bioorg. Med. Chem. Lett. 12 (2002) 1647-1650
    • (2002) Bioorg. Med. Chem. Lett. , vol.12 , pp. 1647-1650
    • Proudfoot, J.R.1
  • 4
    • 0000982054 scopus 로고    scopus 로고
    • Antimicrobial agents: penicillins, cephalosporins, and other β-lactam antibiotics
    • Hardman J.G., and Limbird L.E. (Eds), McGraw-Hill
    • Mandell G.L., and Petri Jr. W.A. Antimicrobial agents: penicillins, cephalosporins, and other β-lactam antibiotics. In: Hardman J.G., and Limbird L.E. (Eds). Goodman & Gilman's The Pharmacological Basis of Therapeutics (1996), McGraw-Hill 1087-1102
    • (1996) Goodman & Gilman's The Pharmacological Basis of Therapeutics , pp. 1087-1102
    • Mandell, G.L.1    Petri Jr., W.A.2
  • 5
    • 33645892239 scopus 로고    scopus 로고
    • Proudfoot, J.R. (2006) Drug likeness and analog based drug discovery. In Analog Based Drug Discovery (Fischer, J., Ganellin, C.R., eds), John Wiley-VCH
  • 7
    • 0034843393 scopus 로고    scopus 로고
    • Timing of analog research in drug discovery
    • Fischer J., and Gere A. Timing of analog research in drug discovery. Pharmazie 56 (2001) 675-682
    • (2001) Pharmazie , vol.56 , pp. 675-682
    • Fischer, J.1    Gere, A.2
  • 8
    • 33645894939 scopus 로고    scopus 로고
    • Optimizing drug therapy by analogs
    • Fischer J., and Ganellin C.R. (Eds), John Wiley-VCH
    • Fischer J. Optimizing drug therapy by analogs. In: Fischer J., and Ganellin C.R. (Eds). Analog Based Drug Discovery (2005), John Wiley-VCH
    • (2005) Analog Based Drug Discovery
    • Fischer, J.1
  • 11
    • 0020395328 scopus 로고
    • Inhibition of lymphocytes-mediated-cytolysis and cyclic AMP phosphodiesterase by erythro-9-(2-hdroxy-3-nonyl)adenine
    • Duncan G.S., et al. Inhibition of lymphocytes-mediated-cytolysis and cyclic AMP phosphodiesterase by erythro-9-(2-hdroxy-3-nonyl)adenine. J. Immunopharmacol. 4 (1982) 79-100
    • (1982) J. Immunopharmacol. , vol.4 , pp. 79-100
    • Duncan, G.S.1
  • 12
    • 0022548645 scopus 로고
    • Selective inhibition of cyclic nucleotide phosphodiesterases of human, bovine and rat aorta
    • Lugnier C., et al. Selective inhibition of cyclic nucleotide phosphodiesterases of human, bovine and rat aorta. Biochem. Pharmacol. 35 (1986) 1743-1751
    • (1986) Biochem. Pharmacol. , vol.35 , pp. 1743-1751
    • Lugnier, C.1
  • 15
    • 84889859264 scopus 로고    scopus 로고
    • Wermuth, C.G. (2006) Analogues as means of discovering new drugs. In Analog Based Drug Discovery (Fischer, J., Ganellin, C.R., eds), John Wiley-VCH
  • 16
    • 0036835460 scopus 로고    scopus 로고
    • Integration of virtual and high-throughput screening
    • Bajorath J. Integration of virtual and high-throughput screening. Nat. Rev. Drug Disc. 1 (2002) 882-894
    • (2002) Nat. Rev. Drug Disc. , vol.1 , pp. 882-894
    • Bajorath, J.1
  • 17
    • 0028875168 scopus 로고
    • BMS-192548, a tetracyclic binding inhibitor of neuropeptide Y receptors, from Aspergillus niger WB2346. II. Physico-chemical properties and structural characterization
    • Shu Y.Z., et al. BMS-192548, a tetracyclic binding inhibitor of neuropeptide Y receptors, from Aspergillus niger WB2346. II. Physico-chemical properties and structural characterization. J. Antibiot. 48 (1995) 1060-1065
    • (1995) J. Antibiot. , vol.48 , pp. 1060-1065
    • Shu, Y.Z.1
  • 18
    • 0023104102 scopus 로고
    • SR 95191 a selective inhibitor of type A monoamine oxidase with dopaminergic properties I. Psychopharmacological profile in Rodents
    • Worms P., et al. SR 95191 a selective inhibitor of type A monoamine oxidase with dopaminergic properties I. Psychopharmacological profile in Rodents. J. Pharmacol. Exp. Ther. 240 (1987) 241-250
    • (1987) J. Pharmacol. Exp. Ther. , vol.240 , pp. 241-250
    • Worms, P.1
  • 19
    • 20144365133 scopus 로고    scopus 로고
    • 2-adrenoceptor blocking activity
    • 2-adrenoceptor blocking activity. J. Med. Chem. 48 (2005) 2054-2071
    • (2005) J. Med. Chem. , vol.48 , pp. 2054-2071
    • Andrès, J.I.1
  • 20
    • 0014232316 scopus 로고
    • Resolution and racemization of dl-Tetramisole, dl-6-Phenyl-2,3,5,6-tetrahydroimidazo-[2,1-b]thiazole
    • Bullock M.W., et al. Resolution and racemization of dl-Tetramisole, dl-6-Phenyl-2,3,5,6-tetrahydroimidazo-[2,1-b]thiazole. J. Med. Chem. 11 (1968) 169-171
    • (1968) J. Med. Chem. , vol.11 , pp. 169-171
    • Bullock, M.W.1
  • 21
    • 0019352301 scopus 로고
    • Levamisole-a general pharmacological perspective
    • Schnieden H. Levamisole-a general pharmacological perspective. Int. J. Immunopharmacol. 3 (1981) 9-13
    • (1981) Int. J. Immunopharmacol. , vol.3 , pp. 9-13
    • Schnieden, H.1
  • 22
    • 0017664338 scopus 로고
    • (+) and (-)-3-methoxycyproheptadine. A comparative evaluation of the antiserotonin, antihistaminic, anticholinergic, and orexigenic properties with cyproheptadine
    • Remy D.C., et al. (+) and (-)-3-methoxycyproheptadine. A comparative evaluation of the antiserotonin, antihistaminic, anticholinergic, and orexigenic properties with cyproheptadine. J. Med. Chem. 20 (1977) 1681-1684
    • (1977) J. Med. Chem. , vol.20 , pp. 1681-1684
    • Remy, D.C.1
  • 23
    • 0342330483 scopus 로고
    • An arylaminopyridazine derivative of γ-aminobutyric acid (GABA) is a selective and competitive antagonist at the GABAA receptor site
    • Chambon J.-P., et al. An arylaminopyridazine derivative of γ-aminobutyric acid (GABA) is a selective and competitive antagonist at the GABAA receptor site. Proc. Natl. Acad. Sci. U. S. A. 82 (1985) 1832-1836
    • (1985) Proc. Natl. Acad. Sci. U. S. A. , vol.82 , pp. 1832-1836
    • Chambon, J.-P.1
  • 24
    • 0000983953 scopus 로고
    • Pyridazinyl-GABA derivatives: a new class of synthetic GABA-A antagonists
    • Wermuth C.G., and Bizière K. Pyridazinyl-GABA derivatives: a new class of synthetic GABA-A antagonists. Trends Pharmacol. Sci. 7 (1986) 421-424
    • (1986) Trends Pharmacol. Sci. , vol.7 , pp. 421-424
    • Wermuth, C.G.1    Bizière, K.2
  • 25
    • 0023152855 scopus 로고
    • Synthesis and structure-activity relationships of a series of aminopyridazine derivatives of γ-aminobutyric acid acting as selective GABA-A antagonists
    • Wermuth C.G., et al. Synthesis and structure-activity relationships of a series of aminopyridazine derivatives of γ-aminobutyric acid acting as selective GABA-A antagonists. J. Med. Chem. 30 (1987) 239-249
    • (1987) J. Med. Chem. , vol.30 , pp. 239-249
    • Wermuth, C.G.1
  • 26
    • 33645873840 scopus 로고
    • The development of pyridazinyl-GABA's, a new class of synthetic GABA antagonists
    • Ravina E. (Ed), Universidade de Santiago de Compostela
    • Wermuth C.G. The development of pyridazinyl-GABA's, a new class of synthetic GABA antagonists. In: Ravina E. (Ed). Ist Spanish-Portuguese Congress of Therapeutical Chemistry (1987), Universidade de Santiago de Compostela 107-140
    • (1987) Ist Spanish-Portuguese Congress of Therapeutical Chemistry , pp. 107-140
    • Wermuth, C.G.1
  • 27
    • 0006730667 scopus 로고
    • Studies on the pyridazine series - pharmacological and therapeutic potential of 3-aminopyridazines
    • Wermuth C.G. Studies on the pyridazine series - pharmacological and therapeutic potential of 3-aminopyridazines. Actualités de Chimie Thérapeutique 12 (1985) 3-35
    • (1985) Actualités de Chimie Thérapeutique , vol.12 , pp. 3-35
    • Wermuth, C.G.1
  • 28
    • 0026772112 scopus 로고
    • Structure and molecular modeling of GABA-A receptor antagonists
    • Rognan D., et al. Structure and molecular modeling of GABA-A receptor antagonists. J. Med. Chem. 35 (1992) 1969-1977
    • (1992) J. Med. Chem. , vol.35 , pp. 1969-1977
    • Rognan, D.1
  • 29
    • 33645895534 scopus 로고
    • Synthèse de (chloro-5 pyridyl-2)-6 (méthyl-4 piperazinyl-1) carbonyloxy-5 oxo-7 dihydro-6,7 5H-pyrrolo[3-4b] pyrazine
    • Jeanmart C., and Cotrel C. Synthèse de (chloro-5 pyridyl-2)-6 (méthyl-4 piperazinyl-1) carbonyloxy-5 oxo-7 dihydro-6,7 5H-pyrrolo[3-4b] pyrazine. Compt. Rend. Acad. Sci. Série C 287 (1978) 377-380
    • (1978) Compt. Rend. Acad. Sci. Série C , vol.287 , pp. 377-380
    • Jeanmart, C.1    Cotrel, C.2
  • 30
    • 0026467552 scopus 로고
    • The pharmacology of cyclopyrrolone derivatives acting at the GABAA/benzodiazepine receptor
    • Doble A., et al. The pharmacology of cyclopyrrolone derivatives acting at the GABAA/benzodiazepine receptor. Adv. Biochem. Psychopharmacol. 47 (1992) 407-418
    • (1992) Adv. Biochem. Psychopharmacol. , vol.47 , pp. 407-418
    • Doble, A.1
  • 31
    • 0021872980 scopus 로고
    • Pharmacological profile of the imidazopyridine zolpidem at benzodiazepine receptors and electrocorticogram in rats
    • Arbilla S., et al. Pharmacological profile of the imidazopyridine zolpidem at benzodiazepine receptors and electrocorticogram in rats. Naunyn Schmiedebergs Arch. Pharmacol. 330 (1985) 248-251
    • (1985) Naunyn Schmiedebergs Arch. Pharmacol. , vol.330 , pp. 248-251
    • Arbilla, S.1
  • 32
    • 0033523672 scopus 로고    scopus 로고
    • 'Scaffold-hopping' by topological pharmacophore search: a contribution to virtual screening
    • Schneider G., et al. 'Scaffold-hopping' by topological pharmacophore search: a contribution to virtual screening. Angew. Chem. Int. Ed. Engl. 38 (1999) 2894-2896
    • (1999) Angew. Chem. Int. Ed. Engl. , vol.38 , pp. 2894-2896
    • Schneider, G.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.