메뉴 건너뛰기




Volumn 53, Issue 5, 1998, Pages 429-437

Melatonin, a suitable lead compound for rational drug design;La melatonine, prototype pertinent pour l'innovation therapeutique

Author keywords

Agomelatin; Drug design; Melatonin; Melatoninergic receptors; Structure activity relationships

Indexed keywords

AGOMELATINE; MELATONIN; MELATONIN RECEPTOR; ACETAMIDE DERIVATIVE; BENZOFURAN DERIVATIVE; BENZOTHIOPHENE; CELL RECEPTOR; CELL SURFACE RECEPTOR; CYCLIC AMP; LIGAND; NAPHTHALENE DERIVATIVE; TETRALIN DERIVATIVE; THIOPHENE DERIVATIVE;

EID: 0032151470     PISSN: 00405957     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper
Times cited : (15)

References (22)
  • 1
    • 0024372287 scopus 로고
    • Melatonin receptors of the ovine pars tuberalis: Characterization and autoradiographical localization
    • Morgan P, Williams L, Davidson G et al. Melatonin receptors of the ovine pars tuberalis: characterization and autoradiographical localization. J Neuro Endocrinol 1989; 1: 1-4.
    • (1989) J Neuro Endocrinol , vol.1 , pp. 1-4
    • Morgan, P.1    Williams, L.2    Davidson, G.3
  • 2
    • 0028054749 scopus 로고
    • Melatonin receptors: Localization, molecular pharmacology and physiological significance
    • Morgan P, Barrett P, Howell E, Helliwell R. Melatonin receptors: localization, molecular pharmacology and physiological significance. Neurochem Int 1994; 24: 101-146.
    • (1994) Neurochem Int , vol.24 , pp. 101-146
    • Morgan, P.1    Barrett, P.2    Howell, E.3    Helliwell, R.4
  • 3
    • 0030276708 scopus 로고    scopus 로고
    • Melatonin in relation to physiology in adult humans
    • Cagnacci A. Melatonin in relation to physiology in adult humans. J Pineal Res 1996; 21: 200-213.
    • (1996) J Pineal Res , vol.21 , pp. 200-213
    • Cagnacci, A.1
  • 4
    • 0028120980 scopus 로고
    • Clinical perspectives for melatonin and its agonists
    • Arendt J. Clinical perspectives for melatonin and its agonists. Biol psychiatry 1994; 1.
    • (1994) Biol Psychiatry , pp. 1
    • Arendt, J.1
  • 6
    • 0030945110 scopus 로고    scopus 로고
    • Variable bioavailability of oral melatonin
    • Di W, Kadva A, Johnston A, Silman R. Variable bioavailability of oral melatonin. N Engl J Med 1997; 336: 1028-1029.
    • (1997) N Engl J Med , vol.336 , pp. 1028-1029
    • Di, W.1    Kadva, A.2    Johnston, A.3    Silman, R.4
  • 7
    • 0024357395 scopus 로고
    • Melatonin inhibits cyclic AMP production in cultured ovine pars tuberalis cells
    • Morgan P, Lawson W, Davidson G, Howell E. Melatonin inhibits cyclic AMP production in cultured ovine pars tuberalis cells. J Mol Endocrinol 1989; 3: R5-R8.
    • (1989) J Mol Endocrinol , vol.3
    • Morgan, P.1    Lawson, W.2    Davidson, G.3    Howell, E.4
  • 8
    • 9344269392 scopus 로고    scopus 로고
    • Synthesis of 2 amido-2,3-dihydro-1H-phenalene derivatives as new conformationally restricted ligands for melatonin receptors
    • Mathé M, Gaudy F, Sicsic S et al. Synthesis of 2 amido-2,3-dihydro-1H-phenalene derivatives as new conformationally restricted ligands for melatonin receptors. J Med Chem 1996; 39: 3089-3095.
    • (1996) J Med Chem , vol.39 , pp. 3089-3095
    • Mathé, M.1    Gaudy, F.2    Sicsic, S.3
  • 10
    • 0028309734 scopus 로고
    • Mapping the melatonin receptor, 2: Synthesis and biological activity of indole derived melatonin analogues with restricted conformations of the C-3 amidoethane side chain
    • Garratt P, Vonhoff S, Rowe S, Sugden D. Mapping the melatonin receptor, 2: Synthesis and biological activity of indole derived melatonin analogues with restricted conformations of the C-3 amidoethane side chain. Bioorg Med Chem Lett 1994; 4: 1559-1564.
    • (1994) Bioorg Med Chem Lett , vol.4 , pp. 1559-1564
    • Garratt, P.1    Vonhoff, S.2    Rowe, S.3    Sugden, D.4
  • 11
    • 0029930956 scopus 로고    scopus 로고
    • Mapping the melatonin receptor, 4: Comparison of the binding affinities of a series of substituted phenylalkylamides ligands
    • Garratt P, Travard S, Vonhoff S. Mapping the melatonin receptor, 4: Comparison of the binding affinities of a series of substituted phenylalkylamides ligands. J Med Chem 1996; 39: 1797-1805.
    • (1996) J Med Chem , vol.39 , pp. 1797-1805
    • Garratt, P.1    Travard, S.2    Vonhoff, S.3
  • 12
    • 0031052115 scopus 로고    scopus 로고
    • 3D quantitative structure-activity relationship of melatonin receptor ligands: A comparative molecular field analysis study
    • Sicsic S, Serraz I, Andrieux J et al. 3D quantitative structure-activity relationship of melatonin receptor ligands: a comparative molecular field analysis study. J Med Chem 1997; 40: 739-748.
    • (1997) J Med Chem , vol.40 , pp. 739-748
    • Sicsic, S.1    Serraz, I.2    Andrieux, J.3
  • 13
    • 0025390935 scopus 로고
    • A semi-empirical molecular orbital program
    • Stewart J. A semi-empirical molecular orbital program. J Comput Aided Mol Des 1990; 4: 1-103.
    • (1990) J Comput Aided Mol des , vol.4 , pp. 1-103
    • Stewart, J.1
  • 14
    • 0023751431 scopus 로고
    • Comparative molecular field analysis (CoMFA), 1: Effect of shape on binding of steroids to carrier proteins
    • Cramer R, Patterson D, Bunce J. Comparative molecular field analysis (CoMFA), 1: Effect of shape on binding of steroids to carrier proteins. J Am Chem Soc 1988; 110: 5959-5967.
    • (1988) J Am Chem Soc , vol.110 , pp. 5959-5967
    • Cramer, R.1    Patterson, D.2    Bunce, J.3
  • 15
    • 0028411658 scopus 로고
    • Molecular lipophilicity potential, a tool in 3D QSAR. Method and applications
    • Gaillard P, Carrupt P, Testa B et al. Molecular lipophilicity potential, a tool in 3D QSAR. Method and applications. J Comput Aided Mol Des 1994; 8: 83-96.
    • (1994) J Comput Aided Mol des , vol.8 , pp. 83-96
    • Gaillard, P.1    Carrupt, P.2    Testa, B.3
  • 16
    • 0028072543 scopus 로고
    • Synthesis and structure-activity relationships of novel naphthalenic and bioisosteric related amidic derivatives as melatonin receptor ligands
    • Depreux P, Lesieur D, Ait Mansour H et al. Synthesis and structure-activity relationships of novel naphthalenic and bioisosteric related amidic derivatives as melatonin receptor ligands. J Med Chem 1994; 37: 3231-3239.
    • (1994) J Med Chem , vol.37 , pp. 3231-3239
    • Depreux, P.1    Lesieur, D.2    Ait Mansour, H.3
  • 17
    • 0028909154 scopus 로고
    • Structural requirements at the melatonin receptor
    • Sugden D, Chong N, Lewis D. Structural requirements at the melatonin receptor. Brit J Pharmacol 1995; 114: 618-623.
    • (1995) Brit J Pharmacol , vol.114 , pp. 618-623
    • Sugden, D.1    Chong, N.2    Lewis, D.3
  • 18
    • 0028310827 scopus 로고
    • Mapping the melatonin receptor, 1: The 5 methoxyl group of melatonin is not an essential requirement for biological activity
    • Garratt P, Jones R, Roxe S, Sugden D. Mapping the melatonin receptor, 1: The 5 methoxyl group of melatonin is not an essential requirement for biological activity. Bioorg Med Chem Lett 1994; 4: 1555-1558.
    • (1994) Bioorg Med Chem Lett , vol.4 , pp. 1555-1558
    • Garratt, P.1    Jones, R.2    Roxe, S.3    Sugden, D.4
  • 19
    • 0016695162 scopus 로고
    • Structure-activity relationships of melatonin and related indoleamines
    • Heward C, Hadley M. Structure-activity relationships of melatonin and related indoleamines. Life Sci 1975; 17: 1167-1178.
    • (1975) Life Sci , vol.17 , pp. 1167-1178
    • Heward, C.1    Hadley, M.2
  • 21
    • 0028306136 scopus 로고
    • Expression cloning of a high affinity melatonin receptor from Xenopus dermal melanophores
    • Ebisawa T, Karne S, Lerner M, Reppert S. Expression cloning of a high affinity melatonin receptor from Xenopus dermal melanophores. Proc Natl Acad Sci USA 1994; 91: 6133-6137.
    • (1994) Proc Natl Acad Sci USA , vol.91 , pp. 6133-6137
    • Ebisawa, T.1    Karne, S.2    Lerner, M.3    Reppert, S.4
  • 22
    • 0029972613 scopus 로고    scopus 로고
    • Melatonin receptors step into the light: Cloning and classification of subtypes
    • Reppert S, Weaver D, Godson C. Melatonin receptors step into the light: cloning and classification of subtypes. Trends Pharmacol Sci 1996; 17: 100-102.
    • (1996) Trends Pharmacol Sci , vol.17 , pp. 100-102
    • Reppert, S.1    Weaver, D.2    Godson, C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.