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Volumn 12, Issue 3, 2003, Pages 147-160

Enzymatic and molecular modeling studies of 5-HT3 receptor ligands based on pyrroloquinoline structure and provided with acetylcholinesterase inhibitory activity

Author keywords

[No Author keywords available]

Indexed keywords

ACETYLCHOLINE; CHOLINESTERASE INHIBITOR; QUINOLINE DERIVATIVE; SEROTONIN 3 AGONIST; TACRINE;

EID: 0942268792     PISSN: 10542523     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (4)

References (12)
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    • Wermuth, C.G.1
  • 4
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    • A New and Rapid Colorimetric Determination of Acetylcholinesterase Activity
    • Ellman, G. L.; Courtney, K. D.; Andres, V.; Featherstone, R. M. A New and Rapid Colorimetric Determination of Acetylcholinesterase Activity. Biochem. Pharmacol. 1961, 7, 88-95.
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    • Ellman, G.L.1    Courtney, K.D.2    Andres, V.3    Featherstone, R.M.4
  • 6
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    • A Quasi-Flexible Automatic Docking Processing for Studying Stereoselective Recognition Mechanisms. Part I. Protocol Validation
    • Alcaro, S.; Gasparrini, F.; Incani, O.; Mecucci, S.; Misiti, D.; Pierini, M.; Villani, C. A Quasi-Flexible Automatic Docking Processing for Studying Stereoselective Recognition Mechanisms. Part I. Protocol Validation. J. Comput. Chem. 2000, 21, 515-530.
    • (2000) J. Comput. Chem. , vol.21 , pp. 515-530
    • Alcaro, S.1    Gasparrini, F.2    Incani, O.3    Mecucci, S.4    Misiti, D.5    Pierini, M.6    Villani, C.7
  • 7
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    • Molecular Modelling and Enzymatic Studies of the Interaction of a Choline Analogue and the Acetylcholinesterase
    • Alcaro, S.; Scipione, L.; Ortuso, F.; Posca, S.; Rispoli, V.; Rotiroti, D. Molecular Modelling and Enzymatic Studies of the Interaction of a Choline Analogue and the Acetylcholinesterase. Bioorg. Med. Chem. Lett. 2002, 12, 0000
    • (2002) Bioorg. Med. Chem. Lett. , vol.12 , pp. 0000
    • Alcaro, S.1    Scipione, L.2    Ortuso, F.3    Posca, S.4    Rispoli, V.5    Rotiroti, D.6
  • 8
    • 0026620007 scopus 로고
    • AMBER* Torsional Parameters for the Peptide Backbone
    • McDonald, D. Q.; Still, W. C. AMBER* Torsional Parameters for the Peptide Backbone, Tetrahedron Lett. 1992, 33, 7743-7746.
    • (1992) Tetrahedron Lett. , vol.33 , pp. 7743-7746
    • McDonald, D.Q.1    Still, W.C.2
  • 9
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    • Semianalytical Treatment of Solvation for Molecular Mechanics and Dynamics
    • Still, W. C.; Tempczyk, A.; Hawley, R. C.; Hendrickson, T. Semianalytical Treatment of Solvation for Molecular Mechanics and Dynamics. J. Am. Chem. Soc. 1990, 112, 6127-6129.
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 6127-6129
    • Still, W.C.1    Tempczyk, A.2    Hawley, R.C.3    Hendrickson, T.4
  • 10
    • 0942265733 scopus 로고    scopus 로고
    • note
    • The two distances have been selected respectively from the amide nitrogen attached in 3′ to the tropane moiety and oxygen of the phenolic group of Tyr121 e Tyr130. The filtering criterion accepted docking configurations with distances respectively lower than 9.5 and 11 Å.
  • 11
    • 0035829449 scopus 로고    scopus 로고
    • Synthesis and Screening for Antiacetylcholinesterase Activity of (1-Benzyl-4-oxopiperidin-3-ylidene) methylindoles and -pyrroles Related to Donepezil
    • Andreani, A.; Cavalli, A.; Granaiola, M.; Guardigli, M.; Leoni, A.; Locatelli, A.; Morigi, R.; Rambaldi, M.; Recanatini, M. and Roda, A. Synthesis and Screening for Antiacetylcholinesterase Activity of (1-Benzyl-4-oxopiperidin- 3-ylidene) methylindoles and -pyrroles Related to Donepezil. J. Med. Chem. 2001, 44, 4011-4014.
    • (2001) J. Med. Chem. , vol.44 , pp. 4011-4014
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    • Kryger, G.1    Silman, I.2    Sussman, L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.