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Volumn 55, Issue 10, 2003, Pages 1397-1404

Synthesis and biological activity of pyridinium-type acetylcholinesterase inhibitors

Author keywords

[No Author keywords available]

Indexed keywords

1 (3 HYDROXYPROPYL) 4 [[(PHTHALIMIDOMETHOXY]IMINO]METHYL]PYRIDINIUM DIBROMIDE; 1 (3 HYDROXYPROPYL) 4 [[[(2 CHLOROPHENYL)METHOXY]IMINO]METHYL]PYRIDINIUM BROMIDE; 1 (3 HYDROXYPROPYL) 4 [[[(2,6 DICHLOROPHENYL)METHOXY]IMINO]METHYL]PYRIDINIUM BROMIDE; 1 (3 PHENYLPROPYL) 4 [[(PHTHALIMIDOMETHOXY]IMINO]METHYL]PYRIDINIUM DIBROMIDE; 1 (3 PHENYLPROPYL) 4 [[[(2 CHLOROPHENYL)METHOXY]IMINO]METHYL]PYRIDINIUM BROMIDE; 1 (3 PHENYLPROPYL) 4 [[[(2,6 DICHLOROPHENYL)METHOXY]IMINO]METHYL]PYRIDINIUM BROMIDE; 1 [3 (4 METHOXYPHENYL)PROPYL] 4 [[(PHTHALIMIDOMETHOXY]IMINO]METHYL]PYRIDINIUM BROMIDE; 1 [3 (4 METHOXYPHENYL)PROPYL] 4 [[[(2 CHLOROPHENYL)METHOXY]IMINO]METHYL]PYRIDINIUM BROMIDE; 1 [3 (4 METHOXYPHENYL)PROPYL] 4 [[[(2,6 DICHLOROPHENYL)METHOXY]IMINO]METHYL]PYRIDINIUM BROMIDE; 1 [3 (PYRIDINIUM 1 YL)PROPYL] 4 [[(PHTHALIMIDOMETHOXY]IMINO]METHYL]PYRIDINIUM DIBROMIDE; 1 [3 (PYRIDINIUM 1 YL)PROPYL] 4 [[[(2 CHLOROPHENYL)METHOXY]IMINO]METHYL]PYRIDINIUM DIBROMIDE; 1 [3 (PYRIDINIUM 1 YL)PROPYL] 4 [[[(2,6 DICHLOROPHENYL)METHOXY]IMINO]METHYL]PYRIDINIUM DIBROMIDE; 1 ETHYL 4 [[(PHTHALIMIDOMETHOXY]IMINO]METHYL]PYRIDINIUM BROMIDE; 1 ETHYL 4 [[[(2 CHLOROPHENYL)METHOXY]IMINO]METHYL]PYRIDINIUM BROMIDE; 1 ETHYL 4 [[[(2,6 DICHLOROPHENYL)METHOXY]IMINO]METHYL]PYRIDINIUM BROMIDE; 1 PROPYL 4 [[(PHTHALIMIDOMETHOXY]IMINO]METHYL]PYRIDINIUM BROMIDE; 1 PROPYL 4 [[[(2 CHLOROPHENYL)METHOXY]IMINO]METHYL]PYRIDINIUM BROMIDE; 1 PROPYL 4 [[[(2,6 DICHLOROPHENYL)METHOXY]IMINO]METHYL]PYRIDINIUM BROMIDE; CHOLINESTERASE; CHOLINESTERASE INHIBITOR; PYRIDINIUM DERIVATIVE; TACRINE; UNCLASSIFIED DRUG;

EID: 0142183252     PISSN: 00223573     EISSN: None     Source Type: Journal    
DOI: 10.1211/0022357021855     Document Type: Article
Times cited : (22)

References (16)
  • 1
    • 0002597710 scopus 로고
    • Molecular modeling and synthesis of potent stabilizers of antagonist binding to M-cholinoceptors
    • Bejeuhr, G., Holzgrabe, U., Mohr, K., Sürig, U., Petersenn, A. (1992) Molecular modeling and synthesis of potent stabilizers of antagonist binding to M-cholinoceptors. Pharm. Pharmacol. Lett. 2: 100-103
    • (1992) Pharm. Pharmacol. Lett. , vol.2 , pp. 100-103
    • Bejeuhr, G.1    Holzgrabe, U.2    Mohr, K.3    Sürig, U.4    Petersenn, A.5
  • 3
    • 0028334668 scopus 로고
    • Search for the pharmacophore of bispyridinium-type allosteric modulators of muscarinic receptors
    • Botero Cid, M. H., Holzgrabe, U., Kostenis, E., Mohr, K., Tränkle, C. (1994) Search for the pharmacophore of bispyridinium-type allosteric modulators of muscarinic receptors. J. Med. Chem. 37: 1439-1445
    • (1994) J. Med. Chem. , vol.37 , pp. 1439-1445
    • Botero Cid, M.H.1    Holzgrabe, U.2    Kostenis, E.3    Mohr, K.4    Tränkle, C.5
  • 4
    • 0035382539 scopus 로고    scopus 로고
    • Dynamic deconvolution of a pre-equilibrated dynamic combinatorial library of acetylcholinesterase inhibitors
    • Bunyapaiboonsri, T., Ramström, O., Lohmann, S., Lehn, J.-M., Peng, L., Goeldner, M. (2001) Dynamic deconvolution of a pre-equilibrated dynamic combinatorial library of acetylcholinesterase inhibitors. Chembiochem. 2: 438-444
    • (2001) Chembiochem. , vol.2 , pp. 438-444
    • Bunyapaiboonsri, T.1    Ramström, O.2    Lohmann, S.3    Lehn, J.-M.4    Peng, L.5    Goeldner, M.6
  • 6
    • 0033575679 scopus 로고    scopus 로고
    • Potent, easily synthesized huperzine A-tacrine hybrid acetylcholinesterase inhibitors
    • Carlier, P. R., Du, D.-M., Han, Y., Liu, J., Pang, Y.-P. (1999b) Potent, easily synthesized huperzine A-tacrine hybrid acetylcholinesterase inhibitors. Bioorg. Med. Chem. Lett. 9: 2335-2338
    • (1999) Bioorg. Med. Chem. Lett. , vol.9 , pp. 2335-2338
    • Carlier, P.R.1    Du, D.-M.2    Han, Y.3    Liu, J.4    Pang, Y.-P.5
  • 7
    • 0041000521 scopus 로고
    • On distribution-free multiple comparisons in the one-way analysis of variance
    • Critchlow, D. E., Fligner, M. A. (1991) On distribution-free multiple comparisons in the one-way analysis of variance. Commun. Statist.-Theory Meth. 20: 127-139
    • (1991) Commun. Statist.-Theory Meth. , vol.20 , pp. 127-139
    • Critchlow, D.E.1    Fligner, M.A.2
  • 8
    • 33644811612 scopus 로고
    • A new and rapid colorimetric determination of acetylcholinesterase activity
    • Ellman, G. L., Coutney, K. D., Andres, V., Featherstone, R. M. (1961) A new and rapid colorimetric determination of acetylcholinesterase activity. Biochem. Pharmacol. 7: 88-95
    • (1961) Biochem. Pharmacol. , vol.7 , pp. 88-95
    • Ellman, G.L.1    Coutney, K.D.2    Andres, V.3    Featherstone, R.M.4
  • 10
    • 0034599814 scopus 로고    scopus 로고
    • Potent acetylcholinesterase inhibitors: Design, synthesis and structure-activity relationships of alkene linked bis-galanthamine and galanthamine-galanthamine salts
    • Guillou, C., Mary, A., Renko, D. Z., Gras, E., Thal, C. (2000) Potent acetylcholinesterase inhibitors: Design, synthesis and structure-activity relationships of alkene linked bis-galanthamine and galanthamine-galanthamine salts. Bioorg. Med. Chem. Lett. 10: 637-639
    • (2000) Bioorg. Med. Chem. Lett. , vol.10 , pp. 637-639
    • Guillou, C.1    Mary, A.2    Renko, D.Z.3    Gras, E.4    Thal, C.5
  • 11
    • 0037161599 scopus 로고    scopus 로고
    • Homodimeric tacrine congeners as acetylcholinesterase inhibitors
    • Hu, M.-L., Wu, L.-J., Hsiao, G., Yen, M.-H. (2002) Homodimeric tacrine congeners as acetylcholinesterase inhibitors. J. Med. Chem. 45: 2277-2282
    • (2002) J. Med. Chem. , vol.45 , pp. 2277-2282
    • Hu, M.-L.1    Wu, L.-J.2    Hsiao, G.3    Yen, M.-H.4
  • 12
    • 0348108039 scopus 로고    scopus 로고
    • Synthesis, biological activity and docking studies of new acetylcholinesterase inhibitors of the bispyridinium type
    • In press
    • Kapková, P., Stiefl, N., Sürig, U., Engels, E., Baumann, K., Holzgrabe, U. (2003) Synthesis, biological activity and docking studies of new acetylcholinesterase inhibitors of the bispyridinium type. Arch. Pharm. Pharm. Med. Chem. In press
    • (2003) Arch. Pharm. Pharm. Med. Chem.
    • Kapková, P.1    Stiefl, N.2    Sürig, U.3    Engels, E.4    Baumann, K.5    Holzgrabe, U.6
  • 13
    • 0032458505 scopus 로고    scopus 로고
    • Three-dimensional structure of a complex of E2020 with acetylcholinesterase from Torpedo californica
    • Kryger, G., Silman, I., Sussman, J. L. (1998) Three-dimensional structure of a complex of E2020 with acetylcholinesterase from Torpedo californica. J. Physiol. Paris 92: 191-194
    • (1998) J. Physiol. Paris , vol.92 , pp. 191-194
    • Kryger, G.1    Silman, I.2    Sussman, J.L.3
  • 15
    • 0027517144 scopus 로고
    • Three distinct domains in the cholinesterase molecule confer selectivity for acetyl- and butyrylcholinesterase inhibitors
    • Radić, Z., Pickering, A. N., Vellom, C. D., Camp, S., Taylor, P. (1993) Three distinct domains in the cholinesterase molecule confer selectivity for acetyl- and butyrylcholinesterase inhibitors. Biochemistry 32: 12074-12084
    • (1993) Biochemistry , vol.32 , pp. 12074-12084
    • Radić, Z.1    Pickering, A.N.2    Vellom, C.D.3    Camp, S.4    Taylor, P.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.