-
1
-
-
0031880242
-
Development of acetylcholinesterase inhibitors in the therapy of Alzheimer's disease
-
Taylor P. Development of acetylcholinesterase inhibitors in the therapy of Alzheimer's disease. Neurology 1998;51(1, suppl 1):S30-S35, S65-S67.
-
(1998)
Neurology
, vol.51
, Issue.1 SUPPL. 1
-
-
Taylor, P.1
-
3
-
-
33845282579
-
Acetylcholinesterase: Enzyme structure, reaction dynamics, and virtual transition states
-
Quinn DM. Acetylcholinesterase: Enzyme structure, reaction dynamics, and virtual transition states. Chem Rev 1987;87:955-979.
-
(1987)
Chem Rev
, vol.87
, pp. 955-979
-
-
Quinn, D.M.1
-
4
-
-
0025778840
-
Atomic structure of acetylcholinesterase from Torpedo californica: A prototypic acetylcholine-binding protein
-
Sussman JL, Harel M, Frolow F, Oefner C, Goldman A, Toker L, Silman I. Atomic structure of acetylcholinesterase from Torpedo californica: A prototypic acetylcholine-binding protein. Science 1991;253:872-879.
-
(1991)
Science
, vol.253
, pp. 872-879
-
-
Sussman, J.L.1
Harel, M.2
Frolow, F.3
Oefner, C.4
Goldman, A.5
Toker, L.6
Silman, I.7
-
5
-
-
0027368530
-
Quaternary ligand binding to aromatic residues in the active-site gorge of acetylcholinesterase
-
Harel M, Schalk I, Ehret-Sabatier L, Bouet F, Goeldner M, Hirth L, Axelsen PH, Silman I, Sussman JL. Quaternary ligand binding to aromatic residues in the active-site gorge of acetylcholinesterase. Proc Natl Acad Sci USA 1993;90:9031-9035.
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 9031-9035
-
-
Harel, M.1
Schalk, I.2
Ehret-Sabatier, L.3
Bouet, F.4
Goeldner, M.5
Hirth, L.6
Axelsen, P.H.7
Silman, I.8
Sussman, J.L.9
-
6
-
-
15844422678
-
The X-ray structure of a transition state analog complex reveals the molecular origins of the catalytic power and substrate specificity of acetylcholinesterase
-
Harel M, Quinn DM, Nair HK, Silman I, Sussman JL. The X-ray structure of a transition state analog complex reveals the molecular origins of the catalytic power and substrate specificity of acetylcholinesterase. J Am Chem Soc 1996;118:2340-2346.
-
(1996)
J Am Chem Soc
, vol.118
, pp. 2340-2346
-
-
Harel, M.1
Quinn, D.M.2
Nair, H.K.3
Silman, I.4
Sussman, J.L.5
-
7
-
-
0033522370
-
"Back door" opening implied by the crystal structure of a carbamylated acetylcholinesterase
-
Bartolucci C, Perola E, Cellai L, Brufani M, Lamba D. "Back door" opening implied by the crystal structure of a carbamylated acetylcholinesterase. Biochemistry 1999;38:5714-5719.
-
(1999)
Biochemistry
, vol.38
, pp. 5714-5719
-
-
Bartolucci, C.1
Perola, E.2
Cellai, L.3
Brufani, M.4
Lamba, D.5
-
8
-
-
0027517144
-
Three distinct domains in the cholinesterase molecule confer selectivity for acetyl- and butyrylcholinesterase inhibitors
-
Radić Z, Pickering N, Vellom DC, Camp S, Taylor P. Three distinct domains in the cholinesterase molecule confer selectivity for acetyl- and butyrylcholinesterase inhibitors. Biochemistry 1993;32:12074-12084.
-
(1993)
Biochemistry
, vol.32
, pp. 12074-12084
-
-
Radić, Z.1
Pickering, N.2
Vellom, D.C.3
Camp, S.4
Taylor, P.5
-
9
-
-
0028047375
-
Conformers of acetylcholinesterase: A mechanism of allosteric control
-
Taylor P, Mayer RH, Himel CM. Conformers of acetylcholinesterase: A mechanism of allosteric control. Mol Pharmacol 1994;45:74-83.
-
(1994)
Mol Pharmacol
, vol.45
, pp. 74-83
-
-
Taylor, P.1
Mayer, R.H.2
Himel, C.M.3
-
10
-
-
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, Jalacie 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
Jalacie, T.3
Hong, F.4
Brimijoin, S.5
-
11
-
-
0000134682
-
Cholinestease inhibitors do more than inhibit cholinesterase
-
Becker R, Giacobini E, editors. Boston: Birkhauser
-
Giacobini E. Cholinestease inhibitors do more than inhibit cholinesterase. In: Becker R, Giacobini E, editors. Alzheimer's disease: Molecular biology to therapy, Boston: Birkhauser; 1997. p 188-204
-
(1997)
Alzheimer's Disease: Molecular Biology to Therapy
, pp. 188-204
-
-
Giacobini, E.1
-
13
-
-
0000605095
-
-
Gilman AG, Nies AS, Rall TW, Taylor P. editors. New York: Macmillan
-
Taylor P. In: Gilman AG, Nies AS, Rall TW, Taylor P. editors. The pharmacological basis of therapeutics, 5th edition. New York: Macmillan; 1975. p 131-150.
-
(1975)
The Pharmacological Basis of Therapeutics, 5th Edition
, pp. 131-150
-
-
Taylor, P.1
-
14
-
-
0037133519
-
Kinetic and structural studies on the interaction of cholinesterases with the anti-Alzheimer drug rivastigmine
-
Bar-On P, Millard CB, Harel M, Dvir H, Enz A, Sussman JL, Silman I. Kinetic and structural studies on the interaction of cholinesterases with the anti-Alzheimer drug rivastigmine. Biochemistry 2002;41:3555-3564.
-
(2002)
Biochemistry
, vol.41
, pp. 3555-3564
-
-
Bar-On, P.1
Millard, C.B.2
Harel, M.3
Dvir, H.4
Enz, A.5
Sussman, J.L.6
Silman, I.7
-
15
-
-
0033379073
-
Molecular recognition by acetylcholinesterase at the peripheral anionic site: Structure-activity relationships for inhibitions by aryl carbamates
-
Lin G, Lai C-Y, Liao W-C. Molecular recognition by acetylcholinesterase at the peripheral anionic site: Structure-activity relationships for inhibitions by aryl carbamates. Bioorg Med Chem 1999;7:2683-2689.
-
(1999)
Bioorg Med Chem
, vol.7
, pp. 2683-2689
-
-
Lin, G.1
Lai, C.-Y.2
Liao, W.-C.3
-
17
-
-
0015789712
-
Recording spectrophotometric method for determination of dissociation and phosphorylation constants for the inhibition of acetylcholinesterase by organophosphates in the presence of substrate
-
Hart GJ, O'Brien RD. Recording spectrophotometric method for determination of dissociation and phosphorylation constants for the inhibition of acetylcholinesterase by organophosphates in the presence of substrate. Biochemistry, 1973;12:2940-2945.
-
(1973)
Biochemistry
, vol.12
, pp. 2940-2945
-
-
Hart, G.J.1
O'Brien, R.D.2
-
18
-
-
0023151506
-
p-Nitrophenyl and cholesteryl-N-alkyl carbamates as inhibitors of cholesterol esterase
-
Hosie L, Sutton LD, Quinn DM. p-Nitrophenyl and cholesteryl-N-alkyl carbamates as inhibitors of cholesterol esterase. J Biol Chem 1987;262:260-264.
-
(1987)
J Biol Chem
, vol.262
, pp. 260-264
-
-
Hosie, L.1
Sutton, L.D.2
Quinn, D.M.3
-
19
-
-
0010706689
-
Structure-reactivity relationships as probes for the inhibition mechanism of cholesterol esterase by aryl carbamates. I. Steady-state kinetics
-
Lin G, Lai C-Y, Liao W-C, Kuo B-H, Lu C-P. Structure-reactivity relationships as probes for the inhibition mechanism of cholesterol esterase by aryl carbamates. I. Steady-state kinetics. J Chin Chem Soc 2000;47:489-500.
-
(2000)
J Chin Chem Soc
, vol.47
, pp. 489-500
-
-
Lin, G.1
Lai, C.-Y.2
Liao, W.-C.3
Kuo, B.-H.4
Lu, C.-P.5
-
21
-
-
5444268469
-
Structure-reactivity relationships as probes for the inhibition mechanism of acetylcholinesterase by aryl carbamates. I. Steady-state kinetics
-
Lin G, Lai C-Y, Liao W-C, Liao B-H, Lu C-P. Structure-reactivity relationships as probes for the inhibition mechanism of acetylcholinesterase by aryl carbamates. I. Steady-state kinetics. J Chin Chem Soc 2003;50:1259-1265.
-
(2003)
J Chin Chem Soc
, vol.50
, pp. 1259-1265
-
-
Lin, G.1
Lai, C.-Y.2
Liao, W.-C.3
Liao, B.-H.4
Lu, C.-P.5
-
22
-
-
0033803011
-
Quantitative structure-activity relationships for the pre-steady-state inhibition of cholesterol esterase by 4-nitrophenyl-N-substituted carbamates
-
Lin G, Liao W-C, Chiou S-Y. Quantitative structure-activity relationships for the pre-steady-state inhibition of cholesterol esterase by 4-nitrophenyl-N-substituted carbamates. Bioorg Med Chem 2000;8:2601-2607.
-
(2000)
Bioorg Med Chem
, vol.8
, pp. 2601-2607
-
-
Lin, G.1
Liao, W.-C.2
Chiou, S.-Y.3
-
26
-
-
0029111479
-
Hammett analysis of the inhibition of pancreatic cholesterol esterase by substituted phenyl-N-butylcarbamate
-
Lin G, Lai C-Y. Hammett analysis of the inhibition of pancreatic cholesterol esterase by substituted phenyl-N-butylcarbamate. Tetrahedron Lett 1995;36:6117-6120.
-
(1995)
Tetrahedron Lett
, vol.36
, pp. 6117-6120
-
-
Lin, G.1
Lai, C.-Y.2
-
27
-
-
0030478552
-
Molecular recognition by cholesterol esterase of active site ligands: Structure-reactivity effects for inhibition by aryl carbamates and subsequent carbamylenzyme turnover
-
Feaster SR, Lee K, Baker N, Hui DY, Quinn DM. Molecular recognition by cholesterol esterase of active site ligands: Structure-reactivity effects for inhibition by aryl carbamates and subsequent carbamylenzyme turnover. Biochemistry 1996;35:16723-16734.
-
(1996)
Biochemistry
, vol.35
, pp. 16723-16734
-
-
Feaster, S.R.1
Lee, K.2
Baker, N.3
Hui, D.Y.4
Quinn, D.M.5
-
28
-
-
0001282182
-
Hammett-Taft cross-interaction correlations for the inhibition mechanism of cholesterol esterase by substituted phenyl N-substituted carbamates
-
Lin G. Hammett-Taft cross-interaction correlations for the inhibition mechanism of cholesterol esterase by substituted phenyl N-substituted carbamates. J Phys Org Chem 2000;13:313-321.
-
(2000)
J Phys Org Chem
, vol.13
, pp. 313-321
-
-
Lin, G.1
-
29
-
-
0030029491
-
Linear free energy relationships of the inhibition of pancreatic cholesterol esterase by 4-nitrophenyl-N-alkylcarbamate
-
Lin G, Lai C-Y. Linear free energy relationships of the inhibition of pancreatic cholesterol esterase by 4-nitrophenyl-N-alkylcarbamate. Tetrahedron Lett 1996;2:193-196.
-
(1996)
Tetrahedron Lett
, vol.2
, pp. 193-196
-
-
Lin, G.1
Lai, C.-Y.2
-
30
-
-
0017076526
-
Structure-activity relationships in acetylcholinesterase reactions. Hydrolysis of non-ionic acetic esters
-
Järv J, Kesvatera T, Aavikasar A. Structure-activity relationships in acetylcholinesterase reactions. Hydrolysis of non-ionic acetic esters. Eur J Biochem 1976;67:315-322.
-
(1976)
Eur J Biochem
, vol.67
, pp. 315-322
-
-
Järv, J.1
Kesvatera, T.2
Aavikasar, A.3
-
31
-
-
0032774638
-
Interaction between the peripheral site residues of human butyrylcholinesterase, D70 and Y332, in binding and hydrolysis of substrates
-
Masson P, Xie W, Foroment M-T, Levitsky V, Fortier P-L, Albaret C, Lockridge O. Interaction between the peripheral site residues of human butyrylcholinesterase, D70 and Y332, in binding and hydrolysis of substrates. Biochim Biophys Acta 1999;1433:281-293.
-
(1999)
Biochim Biophys Acta
, vol.1433
, pp. 281-293
-
-
Masson, P.1
Xie, W.2
Foroment, M.-T.3
Levitsky, V.4
Fortier, P.-L.5
Albaret, C.6
Lockridge, O.7
-
33
-
-
0032517243
-
Enantiomeric inhibitors of cholesterol esterase and acetylcholinesterase
-
Lin G, Tsai Y-C, Liu H-C, Liao W-C, Chang C-H. Enantiomeric inhibitors of cholesterol esterase and acetylcholinesterase. Biochem Biophys Acta 1998;1388:161-174.
-
(1998)
Biochem Biophys Acta
, vol.1388
, pp. 161-174
-
-
Lin, G.1
Tsai, Y.-C.2
Liu, H.-C.3
Liao, W.-C.4
Chang, C.-H.5
-
34
-
-
0032946092
-
Structure-reactivity probes for active site shapes of cholesterol esterase by carbamate inhibitors
-
35905
-
Lin G, Shieh C-T, Tsai Y-C, Hwang C-I, Lu C-P, Chen G-H. Structure-reactivity probes for active site shapes of cholesterol esterase by carbamate inhibitors. Biochem Biophys Acta 1999;35905:161-174.
-
(1999)
Biochem Biophys Acta
, pp. 161-174
-
-
Lin, G.1
Shieh, C.-T.2
Tsai, Y.-C.3
Hwang, C.-I.4
Lu, C.-P.5
Chen, G.-H.6
-
35
-
-
0033520108
-
Structure-reactivity relationships for the inhibition mechanism at the second alkyl-chain-binding site of cholesterol esterase and lipase
-
Lin G, Shieh C-T, Ho H-C, Chouhwang J-Y, Lin W-Y, Lu C-P. Structure-reactivity relationships for the inhibition mechanism at the second alkyl-chain-binding site of cholesterol esterase and lipase. Biochemistry 1999;38:9971-9981.
-
(1999)
Biochemistry
, vol.38
, pp. 9971-9981
-
-
Lin, G.1
Shieh, C.-T.2
Ho, H.-C.3
Chouhwang, J.-Y.4
Lin, W.-Y.5
Lu, C.-P.6
-
36
-
-
0035761595
-
Quantitative structure-activity relationship for the inhibition of Pseudomonas species lipase by 4-nitrophenyl-N-substituted carbamate. I. The steady-state kinetics
-
Lin G, Chouhwang J-Y. Quantitative structure-activity relationship for the inhibition of Pseudomonas species lipase by 4-nitrophenyl-N-substituted carbamate. I. The steady-state kinetics. J Biochem Mol Biol Biophys 2001;5:301-308.
-
(2001)
J Biochem Mol Biol Biophys
, vol.5
, pp. 301-308
-
-
Lin, G.1
Chouhwang, J.-Y.2
-
37
-
-
0242662315
-
Cage amines as the stopper inhibitors of cholinesterase
-
Lin G, Tsai H-J, Tsai, T-H. Cage amines as the stopper inhibitors of cholinesterase. Bioorg Med Chem Lett 2003;13:2887-2890.
-
(2003)
Bioorg Med Chem Lett
, vol.13
, pp. 2887-2890
-
-
Lin, G.1
Tsai, H.-J.2
Tsai, T.-H.3
-
38
-
-
3042655101
-
Structure-reactivity relationships as probes for the inhibition mechanism of cholesterol esterase by aryl carbamates. I. Hammett-Taft cross-interaction correlations
-
Lin G. Structure-reactivity relationships as probes for the inhibition mechanism of cholesterol esterase by aryl carbamates. I. Hammett-Taft cross-interaction correlations. J Chin Chem Soc 2004;51:423-129.
-
(2004)
J Chin Chem Soc
, vol.51
, pp. 423-1129
-
-
Lin, G.1
-
39
-
-
12844263231
-
Ortho effects in quantitative structure activity relationships for acetylcholinesterase inhibition by aryl carbamates
-
in press
-
Lin G, Liu Y-C, Lin Y-F, Wu Y-G. Ortho effects in quantitative structure activity relationships for acetylcholinesterase inhibition by aryl carbamates. J Enz Inh Med Chem (in press).
-
J Enz Inh Med Chem
-
-
Lin, G.1
Liu, Y.-C.2
Lin, Y.-F.3
Wu, Y.-G.4
-
40
-
-
0036251240
-
Inhibition of acetylcholinesterase by physostigmine analogs: Conformational mobility of cysteine loop due to the steric effect of the alkyl chain
-
Gavuzzo E, Pomponi M. Inhibition of acetylcholinesterase by physostigmine analogs: Conformational mobility of cysteine loop due to the steric effect of the alkyl chain. J Biochem Mol Toxicol 2002;16:64-69.
-
(2002)
J Biochem Mol Toxicol
, vol.16
, pp. 64-69
-
-
Gavuzzo, E.1
Pomponi, M.2
-
41
-
-
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
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