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Volumn 43, Issue 11, 2000, Pages 2155-2164

Structure-activity relationships in a series of bisquaternary bisphthalimidine derivatives modulating the muscarinic M2-receptor allosterically

Author keywords

[No Author keywords available]

Indexed keywords

1,6 HEXAMETHYLENEBIS[DIMETHYL(3 PHTHALIMIDOPROPYL)AMMONIUM BROMIDE]; AMMONIUM DERIVATIVE; CARBONYL DERIVATIVE; HEXANE; HYDROGEN; METHYLSCOPOLAMINE; MUSCARINIC M2 RECEPTOR; PHTHALIMIDE DERIVATIVE;

EID: 0000025733     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm991136e     Document Type: Article
Times cited : (78)

References (33)
  • 1
    • 0032076016 scopus 로고    scopus 로고
    • Allosteric modulators of ligand binding to muscarinic acetylcholine receptors
    • Holzgrabe, U.; Mohr, K. Allosteric modulators of ligand binding to muscarinic acetylcholine receptors. Drug Discovery Today 1998, 3, 214-222.
    • (1998) Drug Discovery Today , vol.3 , pp. 214-222
    • Holzgrabe, U.1    Mohr, K.2
  • 5
    • 0028231689 scopus 로고
    • Mechanism of steric and cooperative actions of alcuronium on cardiac muscarinic acetylcholine receptors
    • Proska, J.; Tucek, S. Mechanism of steric and cooperative actions of alcuronium on cardiac muscarinic acetylcholine receptors. Mol. Pharmacol. 1994, 45, 709-717.
    • (1994) Mol. Pharmacol. , vol.45 , pp. 709-717
    • Proska, J.1    Tucek, S.2
  • 7
    • 0027172276 scopus 로고
    • Use of chimeric muscarinic receptors to investigate epitopes involved in allosteric interactions
    • Ellis, J.; Seidenberg, M.; Brann, M. R. Use of chimeric muscarinic receptors to investigate epitopes involved in allosteric interactions. Mol. Pharmacol. 1993, 44, 583-588.
    • (1993) Mol. Pharmacol. , vol.44 , pp. 583-588
    • Ellis, J.1    Seidenberg, M.2    Brann, M.R.3
  • 8
    • 0023819931 scopus 로고
    • 3H-N-methylscopolamine binding in guinea-pig myocardium by an antidote against organophosphorus intoxication
    • 3H-N-methylscopolamine binding in guinea-pig myocardium by an antidote against organophosphorus intoxication. Pharmacol. Toxicol. 1988, 63, 163-168.
    • (1988) Pharmacol. Toxicol. , vol.63 , pp. 163-168
    • Jepsen, K.1    Lüllmann, H.2    Mohr, K.3    Pfeffer, J.4
  • 9
    • 0030207040 scopus 로고    scopus 로고
    • Comparison of structurally different allosteric modulators of muscarinic receptors by self-organizing neural networks
    • Holzgrabe, U.; Wagener, M.; Gasteiger, J. Comparison of structurally different allosteric modulators of muscarinic receptors by self-organizing neural networks. J. Mol. Graph. 1996, 14 185-193.
    • (1996) J. Mol. Graph. , vol.14 , pp. 185-193
    • Holzgrabe, U.1    Wagener, M.2    Gasteiger, J.3
  • 10
    • 0030240344 scopus 로고    scopus 로고
    • Conformational analysis, molecular shape comparison, and pharmacophore identification of different allosteric modulators of muscarinic receptors
    • Holzgrabe, U.; Hopfinger, A. J. Conformational analysis, molecular shape comparison, and pharmacophore identification of different allosteric modulators of muscarinic receptors. J. Chem. Inf. Comput. Sci. 1996, 36, 1018-1024.
    • (1996) J. Chem. Inf. Comput. Sci. , vol.36 , pp. 1018-1024
    • Holzgrabe, U.1    Hopfinger, A.J.2
  • 11
    • 0028256010 scopus 로고
    • A stable and highly potent hexamethonium derivative which modulates muscarinic receptors allosterically in guinea-pig hearts
    • Bejeuhr, G.; Blaschke, G.; Holzgrabe, U.; Mohr, K.; Sürig, U.; Terfloth, G. A stable and highly potent hexamethonium derivative which modulates muscarinic receptors allosterically in guinea-pig hearts. J. Pharm. Pharmacol. 1994, 46, 108-112.
    • (1994) J. Pharm. Pharmacol. , vol.46 , pp. 108-112
    • Bejeuhr, G.1    Blaschke, G.2    Holzgrabe, U.3    Mohr, K.4    Sürig, U.5    Terfloth, G.6
  • 14
    • 0005335535 scopus 로고
    • Produits de reduction du phthalimide; hydroxyphthalimidine et son
    • Dunet, A.; Willemart, A. Produits de reduction du phthalimide; Hydroxyphthalimidine et son. Bull Soc. Chem. 1948, 189, 887-889.
    • (1948) Bull Soc. Chem. , vol.189 , pp. 887-889
    • Dunet, A.1    Willemart, A.2
  • 15
    • 84943841878 scopus 로고
    • Über derivate des phthalizins und isoindols
    • Gabriel, S.; Naumann, A. Über Derivate des Phthalizins und Isoindols Ber. Dt. Chem. Ges. 1893, 26, 705-713.
    • (1893) Ber. Dt. Chem. Ges. , vol.26 , pp. 705-713
    • Gabriel, S.1    Naumann, A.2
  • 16
    • 85027475307 scopus 로고
    • Zur kenntnis des benzylidenphthalids
    • Gabriel, S. Zur Kenntnis des Benzylidenphthalids. Ber. Dt. Chem. Ges. 1885, 18, 1251-2433.
    • (1885) Ber. Dt. Chem. Ges. , vol.18 , pp. 1251-2433
    • Gabriel, S.1
  • 17
    • 0005193614 scopus 로고
    • The structures of 3-benzylidenephthalide - Primary amine adducts and of o-phenylacetylbenzoic acid
    • Marsili, A.; Scartoni, V. The structures of 3-benzylidenephthalide - Primary amine adducts and of o-phenylacetylbenzoic acid. Gazz. Chim. Ital. 1972, 102, 507-516.
    • (1972) Gazz. Chim. Ital. , vol.102 , pp. 507-516
    • Marsili, A.1    Scartoni, V.2
  • 19
    • 0003896535 scopus 로고
    • Mannhold, R., Krogsgaard-Larsen, P., Timmerman, H., Eds.; VCH: Weinheim
    • Kubinyi, H. QSAR: Hansch Analysis and Related Approaches; Mannhold, R., Krogsgaard-Larsen, P., Timmerman, H., Eds.; VCH: Weinheim, 1993.
    • (1993) QSAR: Hansch Analysis and Related Approaches
    • Kubinyi, H.1
  • 21
    • 0025390935 scopus 로고
    • MOPAC: A semiempirical molecular orbital program
    • Stewart, J. J. P. MOPAC: A semiempirical molecular orbital program. J. Comput.-Aided Mol. Design, 1990, 4, 1-105.
    • (1990) J. Comput.-Aided Mol. Design , vol.4 , pp. 1-105
    • Stewart, J.J.P.1
  • 22
    • 0001728908 scopus 로고    scopus 로고
    • Quantum-chemical descriptors in QSAR/QSPR studies
    • Karelson, M.; Lobanov, V. S.; Katritzky, A. R. Quantum-chemical descriptors in QSAR/QSPR studies, Chem. Rev. 1996, 96, 1027-1043.
    • (1996) Chem. Rev. , vol.96 , pp. 1027-1043
    • Karelson, M.1    Lobanov, V.S.2    Katritzky, A.R.3
  • 23
    • 0024998781 scopus 로고
    • Versatile topological structure descriptor for quantitative structure/property studies
    • Clerc, J. T.; Terkovics, A. L. Versatile Topological Structure Descriptor for Quantitative Structure/property Studies. Anal. Chim. Acta 1990, 235, 93-102.
    • (1990) Anal. Chim. Acta , vol.235 , pp. 93-102
    • Clerc, J.T.1    Terkovics, A.L.2
  • 24
    • 0032897177 scopus 로고    scopus 로고
    • Uniform-length molecular descriptors for quantitative structure - Property (QSPR), quantitative structure - Activity (QSAR), classification studies and similarity searching
    • Baumann, K. Uniform-length molecular descriptors for quantitative structure - property (QSPR), quantitative structure - activity (QSAR), classification studies and similarity searching. TrAC 1999, 18, 36-46.
    • (1999) TrAC , vol.18 , pp. 36-46
    • Baumann, K.1
  • 25
    • 33845379303 scopus 로고
    • Atom pairs as molecular features in structure - Activity studies: Definitions and applications
    • Carhart, R. E.; Smith, D. H.; Venkataraghavan, R. Atom pairs as molecular features in structure - activity studies: Definitions and applications. J. Chem. Inf. Comput. Sci. 1985, 25, 64-73.
    • (1985) J. Chem. Inf. Comput. Sci. , vol.25 , pp. 64-73
    • Carhart, R.E.1    Smith, D.H.2    Venkataraghavan, R.3
  • 26
    • 0000130397 scopus 로고
    • The quantitative analysis of structure - Activity relationships
    • Wolff, M. E., Ed.; Wiley: New York, 14
    • Kubinyi, H. The Quantitative Analysis of Structure - Activity Relationships. In Burger's Medicinal Chemistry and Drug Discovery; Wolff, M. E., Ed.; Wiley: New York, 1995; Vol. 1, part IV, 14, pp 497-572.
    • (1995) Burger's Medicinal Chemistry and Drug Discovery , vol.1 , Issue.4 PART , pp. 497-572
    • Kubinyi, H.1
  • 27
    • 0018709674 scopus 로고
    • Chance factors in studies of quantitative structure - Activity relationships
    • Topliss, J. G.; Edwards, R. P. Chance Factors in Studies of Quantitative Structure - Activity Relationships. J. Med. Chem. 1979, 22, 1238-1244.
    • (1979) J. Med. Chem. , vol.22 , pp. 1238-1244
    • Topliss, J.G.1    Edwards, R.P.2
  • 28
    • 0000765554 scopus 로고
    • Statistical validation of QSAR results
    • (van de Water-beemd, H. Ed.), VCH Verlagsgesellschaft, Weinheim, Germany, Chapter 5
    • Wold, S.; Eriksson, L. Statistical Validation of QSAR Results, In: Chemometric Methods in Molecular Design (van de Water-beemd, H. Ed.), VCH Verlagsgesellschaft, Weinheim, Germany, 1995, Chapter 5, p 307-318.
    • (1995) Chemometric Methods in Molecular Design , pp. 307-318
    • Wold, S.1    Eriksson, L.2
  • 30
    • 0002368625 scopus 로고    scopus 로고
    • Intramolecular interactions encoded in lipophilicity: Their nature and significance
    • Pliska, V., Testa, B., van de Waterbeemd Eds.; VCH Verlagsgesellschaft: Weinheim, Germany, Chapter 4
    • Testa, B.; Carrupt, P.-A.; Gaillard, P.; Tsai, R.-S. Intramolecular Interactions Encoded in Lipophilicity: Their Nature and Significance In Lipophilicity in Drug Action and Toxicology; Pliska, V., Testa, B., van de Waterbeemd Eds.; VCH Verlagsgesellschaft: Weinheim, Germany, 1996; Chapter 4, pp 48-71.
    • (1996) Lipophilicity in Drug Action and Toxicology , pp. 48-71
    • Testa, B.1    Carrupt, P.-A.2    Gaillard, P.3    Tsai, R.-S.4
  • 31
    • 0027054955 scopus 로고
    • Two allosteric modulators interact at a common site on cardiac muscarinic receptors
    • Ellis J.; Seidenberg, M. Two allosteric modulators interact at a common site on cardiac muscarinic receptors. Mol. Pharmacol. 1992, 42, 638-641.
    • (1992) Mol. Pharmacol. , vol.42 , pp. 638-641
    • Ellis, J.1    Seidenberg, M.2
  • 32
    • 0029030852 scopus 로고
    • Lock and key in the real world: Concluding remarks
    • Kubinyi, H. Lock and Key in the Real World: Concluding Remarks. Pharm. Acta Helv. 1994, 69, 243-258.
    • (1994) Pharm. Acta Helv. , vol.69 , pp. 243-258
    • Kubinyi, H.1
  • 33
    • 0030433044 scopus 로고    scopus 로고
    • Search for lead structures to develop new allosteric modulators of muscarinic receptors
    • Tränkle, C.; Kostenis, E.; Burgmer, U.; Mohr, K. Search for lead structures to develop new allosteric modulators of muscarinic receptors. J. Pharmacol. Exp. Ther. 1996, 279, 926-933.
    • (1996) J. Pharmacol. Exp. Ther. , vol.279 , pp. 926-933
    • Tränkle, C.1    Kostenis, E.2    Burgmer, U.3    Mohr, K.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.