메뉴 건너뛰기




Volumn 36, Issue 5, 1996, Pages 1018-1024

Conformational analysis, molecular shape comparison, and pharmacophore identification of different allosteric modulators of muscarinic receptors

Author keywords

Allosteric modulators; MSA; Pharmacophore mapping

Indexed keywords

ALCURONIUM; MUSCARINIC RECEPTOR; TRIMEDOXIME;

EID: 0030240344     PISSN: 00952338     EISSN: None     Source Type: Journal    
DOI: 10.1021/ci9502515     Document Type: Article
Times cited : (45)

References (27)
  • 1
    • 0025875643 scopus 로고
    • Allosteric Antagonists of the Muscarinic Acetylcholine Receptor
    • Lee, N. H.; El-Fakahany, E. E. Allosteric Antagonists of the Muscarinic Acetylcholine Receptor. Biochem. Pharmacol. 1991, 42, 199-205.
    • (1991) Biochem. Pharmacol. , vol.42 , pp. 199-205
    • Lee, N.H.1    El-Fakahany, E.E.2
  • 2
    • 0029055030 scopus 로고
    • Allosteric Modulation of Muscarinic Acetylcholine Receptors
    • Tucek, S.; Proska, J. Allosteric Modulation of Muscarinic Acetylcholine Receptors TiPS 1995, 16, 205-212.
    • (1995) TiPS , vol.16 , pp. 205-212
    • Tucek, S.1    Proska, J.2
  • 3
    • 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
  • 4
    • 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
  • 5
    • 0026084739 scopus 로고
    • Allosteric Interactions at the m1, m2 and m3 Muscarinic Receptor Subtypes
    • Lee, N. H.; El-Fakahany, E. E. Allosteric Interactions at the m1, m2 and m3 Muscarinic Receptor Subtypes. J. Pharmacol. Exp. Therapeut. 1991, 256, 468.
    • (1991) J. Pharmacol. Exp. Therapeut. , vol.256 , pp. 468
    • Lee, N.H.1    El-Fakahany, E.E.2
  • 7
    • 0028603576 scopus 로고
    • 2-Receptors of Derivatives of the Alkane-bis-ammonium Compound W84. Comparison with Bispyridinium-type Allosteric Modulators
    • 2-Receptors of Derivatives of the Alkane-bis-ammonium Compound W84. Comparison with Bispyridinium-type Allosteric Modulators. Eur. J. Med. Chem. 1994, 29, 947.
    • (1994) Eur. J. Med. Chem. , vol.29 , pp. 947
    • Kostenis, E.1    Holzgrabe, U.2    Mohr, K.3
  • 8
    • 0023819931 scopus 로고
    • 3H-N-Methylscopolamine Binding in Guinea-Pig Myocardium by an Antidote against Organophosphate Intoxication
    • 3H-N-Methylscopolamine Binding in Guinea-Pig Myocardium by an Antidote against Organophosphate 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
  • 10
    • 0002597710 scopus 로고
    • Molecular Modelling and Synthesis of Potent Stabilizers of Antagonist Binding to M-Cholinoceptors
    • Bejeuhr, G.; Holzgrabe, U.; Mohr, K.; Sürig, U.; v. Petersenn, A. Molecular Modelling and Synthesis of Potent Stabilizers of Antagonist Binding to M-Cholinoceptors. Pharm. Pharmcol. Lett 1992, 2, 100-103.
    • (1992) Pharm. Pharmcol. Lett , vol.2 , pp. 100-103
    • Bejeuhr, G.1    Holzgrabe, U.2    Mohr, K.3    Sürig, U.4    V Petersenn, A.5
  • 11
    • 85033837720 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. In press.
    • J. Mol. Graph. in Press
    • Holzgrabe, U.1    Wagener, M.2    Gasteiger, J.3
  • 12
    • 85033851153 scopus 로고    scopus 로고
    • Personal communication
    • Holzgrabe, U. Personal communication.
    • Holzgrabe, U.1
  • 13
    • 0000490166 scopus 로고
    • From Atoms and Bonds to Three-dimensional Atomic Coordinates: Automatic Model Builders
    • Sadowski, J.; Gasteiger, J. From Atoms and Bonds to Three-dimensional Atomic Coordinates: Automatic Model Builders. Chem. Rev. 1993, 93, 2567-2581.
    • (1993) Chem. Rev. , vol.93 , pp. 2567-2581
    • Sadowski, J.1    Gasteiger, J.2
  • 17
    • 85033857861 scopus 로고
    • Molsim, The Chem 21 Group: 1780 Wilson Drive, Lake Forest, IL 60045
    • Doherty, D. C. Molsim User Guide, Version 3.0; Molsim, The Chem 21 Group: 1780 Wilson Drive, Lake Forest, IL 60045, 1995.
    • (1995) Molsim User Guide, Version 3.0
    • Doherty, D.C.1
  • 19
    • 85030200489 scopus 로고    scopus 로고
    • Molecular Simulations Inc.: 200 Fifth Ave, Waltham, MA 02154
    • QUANTA: Version 3.3; Molecular Simulations Inc.: 200 Fifth Ave, Waltham, MA 02154.
    • QUANTA: Version 3.3
  • 21
    • 0020957990 scopus 로고
    • Theory and Application of Molecular Potential Energy Fields in Molecular Shape Analysis: A Quantitative Structure-Activity Relationship Study of 2,4-Diamino-5-pyrimidines as Dihydrofolate Reductase Inhibitors
    • Hopfinger, A. J. Theory and Application of Molecular Potential Energy Fields in Molecular Shape Analysis: A Quantitative Structure-Activity Relationship Study of 2,4-Diamino-5-pyrimidines as Dihydrofolate Reductase Inhibitors. J. Med. Chem. 1983. 26. 990-996.
    • (1983) J. Med. Chem. , vol.26 , pp. 990-996
    • Hopfinger, A.J.1
  • 22
    • 85033843228 scopus 로고    scopus 로고
    • Hugo Kubinyi, BASF AG, 67056 Ludwigshafen, FRG
    • Hugo Kubinyi, BASF AG, 67056 Ludwigshafen, FRG.
  • 23
    • 0028467707 scopus 로고
    • Application of Genetic Function Approximation to Quantitative Structure-Activity Relationships and Quantitative Structure-Property Relationships
    • Rogers, D.; Hopfinger, A. J. Application of Genetic Function Approximation to Quantitative Structure-Activity Relationships and Quantitative Structure-Property Relationships. J. Chem. Inf. Comput. Sci. 1994, 34, 854-866.
    • (1994) J. Chem. Inf. Comput. Sci. , vol.34 , pp. 854-866
    • Rogers, D.1    Hopfinger, A.J.2
  • 25
    • 0028256010 scopus 로고
    • 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.A.6
  • 26
    • 85033859242 scopus 로고
    • Thesis, Bonn, FRG
    • Nassif-Makki T. Thesis, Bonn, FRG, 1995.
    • (1995)
    • Nassif-Makki, T.1
  • 27
    • 0028334668 scopus 로고
    • Search for the Pharmacophore of Bispyridinium-Type Allosteric Modulators of Muscarinic Receptors
    • Bolero Cid, M. H.; Holzgrabe, U.; Kostenis, E.; Mohr, K.; Tränkle, C. Search for the Pharmacophore of Bispyridinium-Type Allosteric Modulators of Muscarinic Receptors. J. Med. Chem. 1994, 37, 1439-1445.
    • (1994) J. Med. Chem. , vol.37 , pp. 1439-1445
    • Bolero Cid, M.H.1    Holzgrabe, U.2    Kostenis, E.3    Mohr, K.4    Tränkle, C.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.