-
1
-
-
13444278941
-
New symptomatic strategies in Alzheimer's disease
-
Johnson, C. N.; Roland, A.; Upton, N. New Symptomatic Strategies in Alzheimer's Disease. Drug Discovery Today: Ther. Strategies 2004, 1, 13-19.
-
(2004)
Drug Discovery Today: Ther. Strategies
, vol.1
, pp. 13-19
-
-
Johnson, C.N.1
Roland, A.2
Upton, N.3
-
2
-
-
0035807054
-
A structural motif of acetylcholinesterase that promotes amyloid beta-peptide fibril formation
-
De Ferrari, G. V.; Canales, M. A.; Shin, I.; Weiner, L. M.; Silman, I.; Inestrosa, N. C. A Structural Motif of Acetylcholinesterase That Promotes Amyloid Beta-Peptide Fibril Formation. Biochemistry 2001, 40, 10447-10457.
-
(2001)
Biochemistry
, vol.40
, pp. 10447-10457
-
-
De Ferrari, G.V.1
Canales, M.A.2
Shin, I.3
Weiner, L.M.4
Silman, I.5
Inestrosa, N.C.6
-
3
-
-
0033956134
-
The key role of butyrylcholinesterase during neurogenesis and neural disorders: An antisense-5′-butyrylcholinesterase-DNA study
-
Mack, A.; Robitzki, A. The Key Role of Butyrylcholinesterase during Neurogenesis and Neural Disorders: An Antisense-5′-butyrylcholinesterase- DNA Study. Prog. Neurobiol. 2000, 60, 607-628.
-
(2000)
Prog. Neurobiol.
, vol.60
, pp. 607-628
-
-
Mack, A.1
Robitzki, A.2
-
4
-
-
33748570348
-
Drugs that target cholinesterases
-
Buccafusco, J. J., Ed.; Birkhäuser Verlag: Basel, Boston, Berlin
-
Giacobini, E. Drugs That Target Cholinesterases. In Cognitive Enhancing Drugs; Buccafusco, J. J., Ed.; Birkhäuser Verlag: Basel, Boston, Berlin, 2004; pp 11-36.
-
(2004)
Cognitive Enhancing Drugs
, pp. 11-36
-
-
Giacobini, E.1
-
5
-
-
0036315026
-
Inhibition of acetyl- and butyryl-cholinesterase in the cerebrospinal fluid of patients with alzheimer's disease by rivastigmine: Correlation with cognitive benefit
-
Giacobini, E.; Spiegel, R.; Enz, A.; Veroff, A.; Cutler, R. E. Inhibition of Acetyl- and Butyryl-cholinesterase in the Cerebrospinal Fluid of Patients with Alzheimer's Disease by Rivastigmine: Correlation with Cognitive Benefit. J. Neural Transm. 2002, 109, 1053-1065.
-
(2002)
J. Neural Transm.
, vol.109
, pp. 1053-1065
-
-
Giacobini, E.1
Spiegel, R.2
Enz, A.3
Veroff, A.4
Cutler, R.E.5
-
6
-
-
3042684536
-
Bivalent ligands for G protein-coupled receptors
-
Messer, W. S. Bivalent Ligands for G Protein-Coupled Receptors. Curr. Pharm. Des. 2004, 10, 2015-2020.
-
(2004)
Curr. Pharm. Des.
, vol.10
, pp. 2015-2020
-
-
Messer, W.S.1
-
7
-
-
33847663782
-
Agonistic and antagonistic bivalent ligands of serotonin and dopamine receptors including their transporters
-
in press
-
Decker, M.; Lehmann, J. Agonistic and Antagonistic Bivalent Ligands of Serotonin and Dopamine Receptors Including Their Transporters. Curr. Top. Med. Chem., in press.
-
Curr. Top. Med. Chem.
-
-
Decker, M.1
Lehmann, J.2
-
8
-
-
33644851841
-
Dimeric and hybrid anti-Alzheimer drug candidates
-
and references therein
-
Muñoz-Torrero, D.; Camps, P. Dimeric and Hybrid Anti-Alzheimer Drug Candidates. Curr. Med. Chem. 2006, 13, 399-422 and references therein.
-
(2006)
Curr. Med. Chem.
, vol.13
, pp. 399-422
-
-
Muñoz-Torrero, D.1
Camps, P.2
-
9
-
-
0033044911
-
Evaluation of short tether Bis-THA AChE inhibitors. A further test of the dual binding site hypothesis
-
Carlier, P. R.; Han, Y. F.; Chow, E. S.-H.; Li, C. P.-L.; Wang, H.; Lieu, T. X.; Wong, H. S.; Pang, Y. P. Evaluation of Short Tether Bis-THA AChE Inhibitors. A Further Test of the Dual Binding Site Hypothesis. Bioorg. Med. Chem. 1999, 7, 351-357.
-
(1999)
Bioorg. Med. Chem.
, vol.7
, pp. 351-357
-
-
Carlier, P.R.1
Han, Y.F.2
Chow, E.S.-H.3
Li, C.P.-L.4
Wang, H.5
Lieu, T.X.6
Wong, H.S.7
Pang, Y.P.8
-
10
-
-
0035833105
-
Novel and potent tacrine-related hetero- and homobivalent ligands for acetylcholinesterase and butyrylcholinesterase
-
Savini, L.; Campiani, G.; Gaeta, A.; Pellerano, C.; Fattorusso, C.; Chiasserini, L.; Fedorko, J. M.; Saxena, A. Novel and Potent Tacrine-Related Hetero- and Homobivalent Ligands for Acetylcholinesterase and Butyrylcholinesterase. Bioorg. Med. Chem. Lett. 2001, 11, 1779-1782.
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 1779-1782
-
-
Savini, L.1
Campiani, G.2
Gaeta, A.3
Pellerano, C.4
Fattorusso, C.5
Chiasserini, L.6
Fedorko, J.M.7
Saxena, A.8
-
11
-
-
0037413568
-
Specific targeting of acetylcholinesterase and butyrylcholinesterase recognition sites. Rational design of novel, selective, and highly potent cholinesterase inhibitors
-
Savini, L.; Gaeta, A.; Fattorusso, C.; Catalanotti, B.; Campiani, G.; Chiasserini, L.; Pellerano, C.; Novellino, E.; McKissic, D.; Saxena, A. Specific Targeting of Acetylcholinesterase and Butyrylcholinesterase Recognition Sites. Rational Design of Novel, Selective, and Highly Potent Cholinesterase Inhibitors. J. Med. Chem. 2003, 46, 1-4.
-
(2003)
J. Med. Chem.
, vol.46
, pp. 1-4
-
-
Savini, L.1
Gaeta, A.2
Fattorusso, C.3
Catalanotti, B.4
Campiani, G.5
Chiasserini, L.6
Pellerano, C.7
Novellino, E.8
McKissic, D.9
Saxena, A.10
-
12
-
-
20144367586
-
Development of molecular probes for the identification of extra interaction sites in the Mid-Gorge and peripheral sites of butyrylcholinesterase (BuChE). Rational design of novel, selective, and highly potent BuChE inhibitors
-
Campiani, G.; Fattorusso, C.; Butini, S.; Gaeta, A.; Agnusdei, M.; Gemma, S.; Persico, M.; Catalanotti, B.; Savini, L.; Nacci, V.; Novellino, E.; Holloway, H. W.; Greig, N. H.; Belinskaya, T.; Fedorko, J. M.; Saxena, A. Development of Molecular Probes for the Identification of Extra Interaction Sites in the Mid-Gorge and Peripheral Sites of Butyrylcholinesterase (BuChE). Rational Design of Novel, Selective, and Highly Potent BuChE Inhibitors. J. Med. Chem. 2005, 48, 1919-1929.
-
(2005)
J. Med. Chem.
, vol.48
, pp. 1919-1929
-
-
Campiani, G.1
Fattorusso, C.2
Butini, S.3
Gaeta, A.4
Agnusdei, M.5
Gemma, S.6
Persico, M.7
Catalanotti, B.8
Savini, L.9
Nacci, V.10
Novellino, E.11
Holloway, H.W.12
Greig, N.H.13
Belinskaya, T.14
Fedorko, J.M.15
Saxena, A.16
-
13
-
-
13844253966
-
Novel inhibitors of acetyl- and butyrylcholinesterase derived from the alkaloids dehydroevodiamine and rutaecarpine
-
Decker, M. Novel Inhibitors of Acetyl- and Butyrylcholinesterase Derived from the Alkaloids Dehydroevodiamine and Rutaecarpine. Eur. J. Med. Chem. 2005, 40, 305-313.
-
(2005)
Eur. J. Med. Chem.
, vol.40
, pp. 305-313
-
-
Decker, M.1
-
14
-
-
32044459019
-
Novel tricyclic quinazolinimines and related tetracyclic nitrogen bridgehead compounds as cholinesterase inhibitors with selectivity towards butyrylcholinesterase
-
Decker, M.; Krauth, F.; Lehmann, J. Novel Tricyclic Quinazolinimines and Related Tetracyclic Nitrogen Bridgehead Compounds as Cholinesterase Inhibitors with Selectivity towards Butyrylcholinesterase. Bioorg. Med. Chem. 2006, 14, 1966-1977.
-
(2006)
Bioorg. Med. Chem.
, vol.14
, pp. 1966-1977
-
-
Decker, M.1
Krauth, F.2
Lehmann, J.3
-
15
-
-
0030780763
-
Differences in active site Gorge dimensions of cholinesterases revealed by binding of inhibitors to human butyrylcholinesterase
-
Saxena, A.; Redman, A. M. G.; Jiang, X.; Lockridge, O.; Doctor, B. P. Differences in Active Site Gorge Dimensions of Cholinesterases Revealed by Binding of Inhibitors to Human Butyrylcholinesterase. Biochemistry 1997, 36, 14642-14651.
-
(1997)
Biochemistry
, vol.36
, pp. 14642-14651
-
-
Saxena, A.1
Redman, A.M.G.2
Jiang, X.3
Lockridge, O.4
Doctor, B.P.5
-
16
-
-
0029817834
-
Highly potent, selective, and low cost bis-tetrahydroaminacrine inhibitors of acetylcholinesterase. Steps toward novel drugs for treating Alzheimer's disease
-
Pang, Y. P.; Quiram, P.; Jelacic, T.; Hong, F.; Brimijoin, S. Highly Potent, Selective, and Low Cost Bis-tetrahydroaminacrine Inhibitors of Acetylcholinesterase. Steps toward Novel Drugs for Treating Alzheimer's Disease. J. Biol. Chem. 1996, 271, 23646-23649.
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 23646-23649
-
-
Pang, Y.P.1
Quiram, P.2
Jelacic, T.3
Hong, F.4
Brimijoin, S.5
-
17
-
-
84982065662
-
Die reaktion cyclischer lactimäther mit aminocarbonsäuren
-
Petersen, S.; Tietze, E. Die Reaktion cyclischer Lactimäther mit Aminocarbonsäuren. (Reaction of Cyclic Iminium Ethers with Aminocarbonic Acids.) Liebigs Ann. Chem. 1959, 623, 166-176.
-
(1959)
Liebigs Ann. Chem.
, vol.623
, pp. 166-176
-
-
Petersen, S.1
Tietze, E.2
-
18
-
-
0029871519
-
Acetylcholinesterase inhibition by fused dihydroquinazoline compounds
-
Jaén, J. C.; Gregor, V. E.; Lee, C.; Davies, R.; Emmerling, M. Acetylcholinesterase Inhibition by Fused Dihydroquinazoline Compounds. Bioorg. Med. Chem. Lett. 1996, 6, 737-742.
-
(1996)
Bioorg. Med. Chem. Lett.
, vol.6
, pp. 737-742
-
-
Jaén, J.C.1
Gregor, V.E.2
Lee, C.3
Davies, R.4
Emmerling, M.5
-
19
-
-
37049129379
-
Dimroth rearrangement. XVIII. Synthesis and rearrangement of 4-iminoquinazolines and related systems
-
Brown, D. J.; Ienaga, K. Dimroth Rearrangement. XVIII. Synthesis and Rearrangement of 4-Iminoquinazolines and Related Systems. J. Chem. Soc., Perkin Trans. 1 1975, 21, 2182-2185.
-
(1975)
J. Chem. Soc., Perkin Trans. 1
, vol.21
, pp. 2182-2185
-
-
Brown, D.J.1
Ienaga, K.2
-
20
-
-
33644811612
-
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.
-
(1961)
Biochem. Pharmacol.
, vol.7
, pp. 88-95
-
-
Ellman, G.L.1
Courtney, K.D.2
Andres, V.3
Featherstone, R.M.4
|