-
1
-
-
0037135111
-
The amyloid hypothesis of Alzheimer's disease: Progress and problems on the road to therapeutics
-
Hardy J, Selkoe DJ. The amyloid hypothesis of Alzheimer's disease: Progress and problems on the road to therapeutics. Science (Washington, D. C.) 2002; 297: 353-356.
-
(2002)
Science (Washington, D. C.)
, vol.297
, pp. 353-356
-
-
Hardy, J.1
Selkoe, D.J.2
-
2
-
-
0035741357
-
Use of acetylcholinesterase inhibitors in Alzheimer's disease
-
Moghul S, Wilkinson D. Use of acetylcholinesterase inhibitors in Alzheimer's disease. Expert Rev Neurotherapeutics 2001; 1: 61-69.
-
(2001)
Expert Rev. Neurotherapeutics
, vol.1
, pp. 61-69
-
-
Moghul, S.1
Wilkinson, D.2
-
3
-
-
0026031893
-
Tacrine as a treatment for Alzheimer's dementia
-
Relman AS. Tacrine as a treatment for Alzheimer's dementia. N Eng J Med 1990; 324: 349-352.
-
(1990)
N. Eng. J. Med.
, vol.324
, pp. 349-352
-
-
Relman, A.S.1
-
4
-
-
0028316959
-
Hepatotoxic effects of tacrine administration in patients with Alzheimer's disease
-
Watkins PB, Zimmerman HJ, Knapp MJ, Gracon SI, Lewis KW. Hepatotoxic effects of tacrine administration in patients with Alzheimer's disease. J Am Med Assoc 1994; 271: 992-998.
-
(1994)
J. Am. Med. Assoc.
, vol.271
, pp. 992-998
-
-
Watkins, P.B.1
Zimmerman, H.J.2
Knapp, M.J.3
Gracon, S.I.4
Lewis, K.W.5
-
5
-
-
0028823072
-
Synthesis and structure-activity relationships of acetylcholinesterase inhibitors: 1-benzyl-4-[(5,6-dimethoxy-1-oxoindan-2-yl)methyl]-piperidine hydrochloride and related compounds
-
Sugimoto H, Iimura Y, Yamanishi Y, Yamatsu K. Synthesis and structure-activity relationships of acetylcholinesterase inhibitors: 1-benzyl-4-[(5,6-dimethoxy-1-oxoindan-2-yl)methyl]-piperidine hydrochloride and related compounds. J Med Chem 1995; 38: 4821-4829.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 4821-4829
-
-
Sugimoto, H.1
Iimura, Y.2
Yamanishi, Y.3
Yamatsu, K.4
-
6
-
-
0025572193
-
Stereoselectivity of cholinesterase inhibition by galanthamine and tolerance in humans
-
Thomsen T, Bickel U, Fischer JP, Kewitz H. Stereoselectivity of cholinesterase inhibition by galanthamine and tolerance in humans. Eur J Clin Pharmacol 1990; 39: 603.
-
(1990)
Eur. J. Clin. Pharmacol.
, vol.39
, pp. 603
-
-
Thomsen, T.1
Bickel, U.2
Fischer, J.P.3
Kewitz, H.4
-
7
-
-
0031718551
-
Clinical pharmacology of rivastigmine: A new-generation acetylcholinesterase inhibitor for the treatment of Alzheimer's disease
-
Polinsky RJ. Clinical pharmacology of rivastigmine: A new-generation acetylcholinesterase inhibitor for the treatment of Alzheimer's disease. Clin Therap 1998; 20: 634-647.
-
(1998)
Clin. Therap.
, vol.20
, pp. 634-647
-
-
Polinsky, R.J.1
-
8
-
-
0003161506
-
Preclinical and clinical progress with huperzine A: A novel acetylcholinesterase inhibitor
-
Becker R, Giacobini E, editors. Boston: Birkhäuser
-
Han Y, Tang X. Preclinical and clinical progress with huperzine A: A novel acetylcholinesterase inhibitor. In: Becker R, Giacobini E, editors. Alzheimer disease: From molecular biology to therapy. Boston: Birkhäuser; 1996; p. 245-250.
-
(1996)
Alzheimer Disease: From Molecular Biology to Therapy
, pp. 245-250
-
-
Han, Y.1
Tang, X.2
-
9
-
-
0345034775
-
Chemistry, pharmacology, and clinical efficacy of the chinese nootropic agent huperzine A
-
Kozikowski AP, Tückmantel W. Chemistry, pharmacology, and clinical efficacy of the chinese nootropic agent huperzine A. Acc Chem Res 1999; 32: 641-650.
-
(1999)
Acc. Chem. Res.
, vol.32
, pp. 641-650
-
-
Kozikowski, A.P.1
Tückmantel, W.2
-
10
-
-
0032771261
-
Huperzine A: A novel acetylcholinesterase inhibitor
-
Tang XC, He XC, Bai DL. Huperzine A: A novel acetylcholinesterase inhibitor. Drugs Future 1999; 24: 647-663.
-
(1999)
Drugs Future
, vol.24
, pp. 647-663
-
-
Tang, X.C.1
He, X.C.2
Bai, D.L.3
-
11
-
-
0029863697
-
Acetylcholinesterase accelerates assembly of amyloid-β-peptides into Alzheimer's fibrils: Possible role of the peripheral site of the enzyme
-
Inestrosa NC, Alvarez A, Perez CA, Moreno RD, Vicente M, Linker C, et al. Acetylcholinesterase accelerates assembly of amyloid-β-peptides into Alzheimer's fibrils: Possible role of the peripheral site of the enzyme. Neuron 1996; 16: 881-896.
-
(1996)
Neuron
, vol.16
, pp. 881-896
-
-
Inestrosa, N.C.1
Alvarez, A.2
Perez, C.A.3
Moreno, R.D.4
Vicente, M.5
Linker, C.6
-
12
-
-
0035468115
-
Peripheral and dual binding site acetylcholinesterase inhibitors: Implications in treatment of Alzheimer's disease
-
Castro A, Martinez A. Peripheral and dual binding site acetylcholinesterase inhibitors: Implications in treatment of Alzheimer's disease. Mini Rev Med Chem 2001; 1: 267-272.
-
(2001)
Mini Rev. Med. Chem.
, vol.1
, pp. 267-272
-
-
Castro, A.1
Martinez, A.2
-
13
-
-
0242475195
-
Peripheral and dual binding site inhibitors of acetylcholinesterase as neurodegenerative disease-modifying agents
-
Dorronsoro I, Castro A, Martinez A. Peripheral and dual binding site inhibitors of acetylcholinesterase as neurodegenerative disease-modifying agents. Exp Opin Ther Patents 2003; 13: 1725-1732.
-
(2003)
Exp. Opin. Ther. Patents
, vol.13
, pp. 1725-1732
-
-
Dorronsoro, I.1
Castro, A.2
Martinez, A.3
-
14
-
-
0033103478
-
Structure of acetylcholinesterase complexed with E2020 (Aricept®): Implications for the design of new anti-Alzheimer drugs
-
Kryger G, Silman I, Sussman JL. Structure of acetylcholinesterase complexed with E2020 (Aricept®): Implications for the design of new anti-Alzheimer drugs. Structure 1999; 7: 297-307.
-
(1999)
Structure
, vol.7
, pp. 297-307
-
-
Kryger, G.1
Silman, I.2
Sussman, J.L.3
-
15
-
-
51149208227
-
Curare-like action of polymethylene bisquaternary ammonium salts
-
Paton WDM, Zaimis EJ. Curare-like action of polymethylene bisquaternary ammonium salts. Nature 1948; 161: 718-719.
-
(1948)
Nature
, vol.161
, pp. 718-719
-
-
Paton, W.D.M.1
Zaimis, E.J.2
-
16
-
-
84958116069
-
The pharmacological actions of polymethylene bistrimethylammonium salts
-
Paton WDM, Zaimis EJ. The pharmacological actions of polymethylene bistrimethylammonium salts. Br J Pharmacol 1949; 4: 381-400.
-
(1949)
Br. J. Pharmacol.
, vol.4
, pp. 381-400
-
-
Paton, W.D.M.1
Zaimis, E.J.2
-
17
-
-
0001107286
-
The inhibitory effect of stilbamidine, curare, and related compounds and its relationship to the active groups of acetylcholine esterase. Action of stilbamidine on nerve impulse conduction
-
Bergmann F, Wilson IB, Nachmansohn D. The inhibitory effect of stilbamidine, curare, and related compounds and its relationship to the active groups of acetylcholine esterase. Action of stilbamidine on nerve impulse conduction. Biochim Biophys Acta 1950; 6: 217-224.
-
(1950)
Biochim. Biophys. Acta
, vol.6
, pp. 217-224
-
-
Bergmann, F.1
Wilson, I.B.2
Nachmansohn, D.3
-
18
-
-
0009468617
-
The relationship of quaternary ammonium salts to the anionic sites of true and pseudo cholinesterase
-
Bergmann F, Segal R. The relationship of quaternary ammonium salts to the anionic sites of true and pseudo cholinesterase. Biochem J 1954; 58: 692-698.
-
(1954)
Biochem. J.
, vol.58
, pp. 692-698
-
-
Bergmann, F.1
Segal, R.2
-
19
-
-
0001537321
-
Two selective inhibitors of cholinesterase
-
Austin L, Berry WK. Two selective inhibitors of cholinesterase. Biochem J 1953; 54: 695-700.
-
(1953)
Biochem. J.
, vol.54
, pp. 695-700
-
-
Austin, L.1
Berry, W.K.2
-
20
-
-
0010841263
-
An investigation of the structure-activity correlations within a series of ambenonium analogs
-
Lands AM, Hoppe JO, Arnold A, Kirchner FK. An investigation of the structure-activity correlations within a series of ambenonium analogs. J Pharmacol Exp Ther 1958; 123: 121-127.
-
(1958)
J. Pharmacol. Exp. Ther.
, vol.123
, pp. 121-127
-
-
Lands, A.M.1
Hoppe, J.O.2
Arnold, A.3
Kirchner, F.K.4
-
21
-
-
4544294040
-
Affinity of benzoquinonium and ambenonium derivatives for the acetylcholine receptor, tested on the electroplax, and for acetylcholinesterase in solution
-
Webb GD. Affinity of benzoquinonium and ambenonium derivatives for the acetylcholine receptor, tested on the electroplax, and for acetylcholinesterase in solution. Biochim Biophys Acta 1965; 102: 172-184.
-
(1965)
Biochim. Biophys. Acta
, vol.102
, pp. 172-184
-
-
Webb, G.D.1
-
22
-
-
0027092277
-
Ambenonium is a rapidly reversible noncovalent inhibitor of acetylcholinesterase, with one of the highest known affinities
-
Hodge AS, Humphrey DR, Rosenberry TL. Ambenonium is a rapidly reversible noncovalent inhibitor of acetylcholinesterase, with one of the highest known affinities. Mol Pharmacol 1992; 41: 937-942.
-
(1992)
Mol. Pharmacol.
, vol.41
, pp. 937-942
-
-
Hodge, A.S.1
Humphrey, D.R.2
Rosenberry, T.L.3
-
23
-
-
0015522976
-
Fluorescent probes of acetylcholinesterase
-
Mooser G, Schulman H, Sigman DS. Fluorescent probes of acetylcholinesterase. Biochem 1972; 11: 1595-1602.
-
(1972)
Biochem.
, vol.11
, pp. 1595-1602
-
-
Mooser, G.1
Schulman, H.2
Sigman, D.S.3
-
24
-
-
0016152998
-
Ligand binding properties of acetylcholinesterase determined with fluorescent probes
-
Mooser G, Sigman DS. Ligand binding properties of acetylcholinesterase determined with fluorescent probes. Biochem 1974; 13: 2299-2307.
-
(1974)
Biochem.
, vol.13
, pp. 2299-2307
-
-
Mooser, G.1
Sigman, D.S.2
-
25
-
-
0013945471
-
Responses of acetylcholinesterase from Torpedo marmorata to salts and curarizing drugs
-
Changeux J-P. Responses of acetylcholinesterase from Torpedo marmorata to salts and curarizing drugs. Mol Pharmacol 1966; 2: 369-392.
-
(1966)
Mol. Pharmacol.
, vol.2
, pp. 369-392
-
-
Changeux, J.-P.1
-
26
-
-
0016823110
-
Interaction of fluorescence probes with acetylcholinesterase. The site and specificity of propidium binding
-
Taylor P, Lappi S. Interaction of fluorescence probes with acetylcholinesterase. The site and specificity of propidium binding. Biochem 1975; 14: 1989-1997.
-
(1975)
Biochem.
, vol.14
, pp. 1989-1997
-
-
Taylor, P.1
Lappi, S.2
-
27
-
-
0023179342
-
Site selectivity of fluorescent bisquaternary phenanthridinium ligands for acetylcholinesterase
-
Berman HA, Decker MM, Nowak MW, Leonard KJ, McCauley M, Baker WM, et al. Site selectivity of fluorescent bisquaternary phenanthridinium ligands for acetylcholinesterase. Mol Pharmacol 1987; 31: 610-616.
-
(1987)
Mol. Pharmacol.
, vol.31
, pp. 610-616
-
-
Berman, H.A.1
Decker, M.M.2
Nowak, M.W.3
Leonard, K.J.4
McCauley, M.5
Baker, W.M.6
-
28
-
-
0025778840
-
Atomic structure of acetylcholinesterase from Torpedo californica: A prototype acetylcholine-binding protein
-
Sussman JL, Harel M, Frolow F, Oefner C, Goldman A, Toker L, et al. Atomic structure of acetylcholinesterase from Torpedo californica: A prototype acetylcholine-binding protein. Science (Washington, D.C.) 1991; 253: 872-879.
-
(1991)
Science (Washington,. D.C.)
, vol.253
, pp. 872-879
-
-
Sussman, J.L.1
Harel, M.2
Frolow, F.3
Oefner, C.4
Goldman, A.5
Toker, L.6
-
29
-
-
0027368530
-
Quaternary ligand binding to aromatic residues in the activesite gorge of acetylcholinesterase
-
Hard M, Schalk I, Ehret-Sabatier L, Bouet F, Goeldner M, Hirth C, et al. Quaternary ligand binding to aromatic residues in the activesite gorge of acetylcholinesterase. Proc Natl Acad Sci USA 1993; 90: 9031-9035.
-
(1993)
Proc. Natl. Acad. Sci. USA
, vol.90
, pp. 9031-9035
-
-
Hard, M.1
Schalk, I.2
Ehret-Sabatier, L.3
Bouet, F.4
Goeldner, M.5
Hirth, C.6
-
30
-
-
0030033588
-
Cation-π interactions in chemistry and biology: A new view of benzene, Phe, Tyr, and Trp
-
Dougherty DA. Cation-π interactions in chemistry and biology: A new view of benzene, Phe, Tyr, and Trp. Science (Washington, D C) 1996; 271: 163-168.
-
(1996)
Science (Washington,. D C)
, vol.271
, pp. 163-168
-
-
Dougherty, D.A.1
-
31
-
-
0031015343
-
Structure of acetylcholinesterase complexed with the nootropic alkaloid (-)-huperzine A
-
Raves ML, Harel M, Pang Y-P, Silman I, Kozikowski AP, Sussman JL. Structure of acetylcholinesterase complexed with the nootropic alkaloid (-)-huperzine A. Nature Struct Biol 1997; 4: 57-63.
-
(1997)
Nature Struct. Biol.
, vol.4
, pp. 57-63
-
-
Raves, M.L.1
Harel, M.2
Pang, Y.-P.3
Silman, I.4
Kozikowski, A.P.5
Sussman, J.L.6
-
32
-
-
0033408510
-
Structure of acetylcholinesterase complexed with (-)-galanthamine at 2.3 Å resolution
-
Greenblatt HM, Kryger G, Lewis T, Silman I, Sussman JL. Structure of acetylcholinesterase complexed with (-)-galanthamine at 2.3 Å resolution. FEBS Lett 1999; 463: 321-326.
-
(1999)
FEBS Lett.
, vol.463
, pp. 321-326
-
-
Greenblatt, H.M.1
Kryger, G.2
Lewis, T.3
Silman, I.4
Sussman, J.L.5
-
33
-
-
0036793068
-
Structure of a complex of the potent and specific inhibitor BW 284c51 with Torpedo californica acetylcholinesterase
-
Felder CE, Harel M, Silman I, Sussman JL. Structure of a complex of the potent and specific inhibitor BW 284c51 with Torpedo californica acetylcholinesterase. Acta Crystallogr, Sect D 2002; 58: 1765-1771.
-
(2002)
Acta Crystallogr, Sect. D.
, vol.58
, pp. 1765-1771
-
-
Felder, C.E.1
Harel, M.2
Silman, I.3
Sussman, J.L.4
-
34
-
-
0037413712
-
Structural insights into ligand interactions at the acetylcholinesterase peripheral anionic site
-
Bourne Y, Taylor P, Radic Z, Marchot P. Structural insights into ligand interactions at the acetylcholinesterase peripheral anionic site. EMBO J 2003; 22: 1-12.
-
(2003)
EMBO J.
, vol.22
, pp. 1-12
-
-
Bourne, Y.1
Taylor, P.2
Radic, Z.3
Marchot, P.4
-
35
-
-
0022902748
-
The relationship of spacer length and selectivity at multiple opioid receptors
-
Portoghese PS, Larson DL, Yim CB, Sayre LM, Ronsisvalle G, Tam SW, et al. The relationship of spacer length and selectivity at multiple opioid receptors. J Med Chem 1986; 29: 1855-1861.
-
(1986)
J. Med. Chem.
, vol.29
, pp. 1855-1861
-
-
Portoghese, P.S.1
Larson, D.L.2
Yim, C.B.3
Sayre, L.M.4
Ronsisvalle, G.5
Tam, S.W.6
-
36
-
-
0024405504
-
Bivalent ligands and the message-address concept in the design of selective opioid receptor antagonists
-
Portoghese PS. Bivalent ligands and the message-address concept in the design of selective opioid receptor antagonists. Trends Pharm Sci 1989; 10: 230-235.
-
(1989)
Trends Pharm. Sci.
, vol.10
, pp. 230-235
-
-
Portoghese, P.S.1
-
37
-
-
0027128743
-
The role of concepts in structure-activity relationship studies of opioid ligands
-
Portoghese PS. The role of concepts in structure-activity relationship studies of opioid ligands. J Med Chem 1992; 35: 1927-1937.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 1927-1937
-
-
Portoghese, P.S.1
-
38
-
-
0019407381
-
On the attibution and additivity of binding energies
-
Jencks WP. On the attibution and additivity of binding energies. Proc Natl Acad Sci USA 1981; 78: 4046-4050.
-
(1981)
Proc. Natl. Acad. Sci. USA
, vol.78
, pp. 4046-4050
-
-
Jencks, W.P.1
-
39
-
-
0028693767
-
Prediction of the binding sites of huperzine A in acetylcholinesterase by docking studies
-
Pang Y-P, Kozikowski AP. Prediction of the binding sites of huperzine A in acetylcholinesterase by docking studies. J Comput-Aided Mol Design 1994; 8: 669-681.
-
(1994)
J. Comput-Aided Mol. Design
, vol.8
, pp. 669-681
-
-
Pang, Y.-P.1
Kozikowski, A.P.2
-
40
-
-
0029817834
-
Highly potent, selective, and low cost bis-tetrahydroaminacrine inhibitors of acetylcholinesterase
-
Pang Y-P, Quiram P, Jelacic T, Hong F, Brimijoin S. Highly potent, selective, and low cost bis-tetrahydroaminacrine inhibitors of acetylcholinesterase. 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
-
41
-
-
33748727771
-
Synthesis of alkylene linked bis-THA and alkylene linked benzyl-THA as highly potent and selective inhibitors and molecular probes of acetylcholinesterase
-
Pang Y-P, Hong F, Quiram P, Jelacic T, Brimijoin S. Synthesis of alkylene linked bis-THA and alkylene linked benzyl-THA as highly potent and selective inhibitors and molecular probes of acetylcholinesterase. J Chem Soc Perkin Trans I 1997; 171-176.
-
(1997)
J. Chem. Soc. Perkin Trans. I
, pp. 171-176
-
-
Pang, Y.-P.1
Hong, F.2
Quiram, P.3
Jelacic, T.4
Brimijoin, S.5
-
42
-
-
0033044911
-
Evaluation of short-tether bis-THA AChE inhibitors. A further test of the dual binding site hypothesis
-
Carlier PR, Han YF, Chow ES-H, Li CP-L, Wang H, Lieu TX, et al. 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
-
43
-
-
0033577193
-
Effects of bis(7)-tacrine, a novel anti-Alzheimer's agent, on rat brain AChE
-
Wang H, Carlier PR, Ho WL, Wu DC, Lee NTK, Li CPL, et al. Effects of bis(7)-tacrine, a novel anti-Alzheimer's agent, on rat brain AChE. NeuroReport 1999; 10: 789-793.
-
(1999)
NeuroReport
, vol.10
, pp. 789-793
-
-
Wang, H.1
Carlier, P.R.2
Ho, W.L.3
Wu, D.C.4
Lee, N.T.K.5
Li, C.P.L.6
-
44
-
-
13044286787
-
Attenuation of scopolamine-induced deficits in navigational performance in rats by bis(7)-tacrine, a novel dimeric AChE inhibitor
-
Wang H, Carlier PR, Ho WL, Lee NT-K, Pang Y-P, Han Y-F. Attenuation of scopolamine-induced deficits in navigational performance in rats by bis(7)-tacrine, a novel dimeric AChE inhibitor. Acta Pharm Sin 1999; 20: 211-217.
-
(1999)
Acta Pharm. Sin.
, vol.20
, pp. 211-217
-
-
Wang, H.1
Carlier, P.R.2
Ho, W.L.3
Lee, N.T.-K.4
Pang, Y.-P.5
Han, Y.-F.6
-
45
-
-
0034708402
-
Bis(7)-tacrine, a novel AChE-inhibitor, reverses AF64A-induced deficits in navigational memory in rats
-
Liu J, Ho W-L, Lee NTK, Carlier PR, Pang Y-P, Ian Y. Bis(7)-tacrine, a novel AChE-inhibitor, reverses AF64A-induced deficits in navigational memory in rats. Neurosci Lett 1999; 282: 165-168.
-
(1999)
Neurosci. Lett.
, vol.282
, pp. 165-168
-
-
Liu, J.1
Ho, W.-L.2
Lee, N.T.K.3
Carlier, P.R.4
Pang, Y.-P.5
Ian, Y.6
-
46
-
-
0033533794
-
Heterodimeric tacrine-based acetylcholinesterase inhibitors: Investigating ligand-peripheral site interactions
-
Carlier PR, Chow ES-H, Han Y, Liu J, Yazal JE, Pang Y-P. Heterodimeric tacrine-based acetylcholinesterase inhibitors: Investigating ligand-peripheral site interactions. J Med Chem 1999; 42: 4225-4231.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 4225-4231
-
-
Carlier, P.R.1
Chow, E.S.-H.2
Han, Y.3
Liu, J.4
Yazal, J.E.5
Pang, Y.-P.6
-
48
-
-
0027963184
-
2+ in blockade of the N-methyl-D-aspartate receptor channel
-
2+ in blockade of the N-methyl-D-aspartate receptor channel. Mol Pharmacol 1994; 46: 151-160.
-
(1994)
Mol. Pharmacol.
, vol.46
, pp. 151-160
-
-
Nelson, M.E.1
Albuquerque, E.X.2
-
49
-
-
0030474273
-
Polyamine analogue regulation of NMDA MK-801 binding: A structure-activity study
-
Bergeron RJ, Weimar WR, Wu Q, Feng Y, McManis JS. Polyamine analogue regulation of NMDA MK-801 binding: A structure-activity study. J Med Chem 1996; 39: 5257-5266.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 5257-5266
-
-
Bergeron, R.J.1
Weimar, W.R.2
Wu, Q.3
Feng, Y.4
McManis, J.S.5
-
50
-
-
0001564454
-
Dual-site binding of bivalent 4-aminopyridine and 4-aminoquinoline-based AChE inhibitors: Contribution of the hydrophobic alkylene tether to monomer and dimer affinities
-
Han YF, Li CP-L, Chow ES-H, Wang H, Pang Y-P, Carlier PR. Dual-site binding of bivalent 4-aminopyridine and 4-aminoquinoline-based AChE inhibitors: Contribution of the hydrophobic alkylene tether to monomer and dimer affinities. Bioorg Med Chem 1999; 7: 2569-2575.
-
(1999)
Bioorg. Med. Chem.
, vol.7
, pp. 2569-2575
-
-
Han, Y.F.1
Li, C.P.-L.2
Chow, E.S.-H.3
Wang, H.4
Pang, Y.-P.5
Carlier, P.R.6
-
52
-
-
0014543771
-
N4,N4′-decamethylenebis-4-aminopyridine and N9,N9′-decamethyl-9-aminoacridine
-
Paolini JP, Lendvay LJ, Palopoli FP. N4,N4′-decamethylenebis-4-aminopyridine and N9,N9′-decamethyl-9-aminoacridine. J Med Chem 1969; 12: 701-702.
-
(1969)
J. Med. Chem.
, vol.12
, pp. 701-702
-
-
Paolini, J.P.1
Lendvay, L.J.2
Palopoli, F.P.3
-
53
-
-
0034657522
-
Dimerization of an inactive fragment of huperzine A produces a drug with twice the potency of the natural product
-
Carlier PR, Du D-M, Han Y-F, Liu J, Perola E, Williams ID, et al. Dimerization of an inactive fragment of huperzine A produces a drug with twice the potency of the natural product. Angew Chem Int Ed 2000; 39: 1775-1777.
-
(2000)
Angew Chem. Int. Ed.
, vol.39
, pp. 1775-1777
-
-
Carlier, P.R.1
Du, D.-M.2
Han, Y.-F.3
Liu, J.4
Perola, E.5
Williams, I.D.6
-
54
-
-
0030989863
-
Studies on a new series of THA analogues: Effects of the aromatic residues that line the gorge of AChE
-
Pomponi M, Marta M, Colella A, Sacchi S, Patamia M, Gatta F, et al. Studies on a new series of THA analogues: Effects of the aromatic residues that line the gorge of AChE. FEBS Lett 1997; 409: 155-160.
-
(1997)
FEBS Lett.
, vol.409
, pp. 155-160
-
-
Pomponi, M.1
Marta, M.2
Colella, A.3
Sacchi, S.4
Patamia, M.5
Gatta, F.6
-
55
-
-
0035833105
-
Novel and potent tacrine-related hetero- and homobivalent ligands for acetylcholinesterase and butyrylcholinesterase
-
Savini L, Campiani G, Gaeta A, Pellerano C, Fattoruso C, Chiasserini L, et al. 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
Fattoruso, C.5
Chiasserini, L.6
-
56
-
-
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, et al. 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
-
57
-
-
0037161599
-
Homodimeric tacrine congeners as acetylcholinesterase inhibitors
-
Hu M-K, Wu L-J, Hsiao G, Yen M-H. Homodimeric tacrine congeners as acetylcholinesterase inhibitors. J Med Chem 2002; 45: 2277-2282.
-
(2002)
J. Med. Chem.
, vol.45
, pp. 2277-2282
-
-
Hu, M.-K.1
Wu, L.-J.2
Hsiao, G.3
Yen, M.-H.4
-
58
-
-
0026774930
-
The synthesis and in vitro acetylcholinesterase and butyrylcholinesterase inhibitory activity of tacrine (Cognex®) derivatives
-
Gregor VE, Emmerling MR, Lee C, Moore CJ. The synthesis and in vitro acetylcholinesterase and butyrylcholinesterase inhibitory activity of tacrine (Cognex®) derivatives. Bioorg Med Chem Lett 1992; 2: 861-864.
-
(1992)
Bioorg. Med. Chem. Lett.
, vol.2
, pp. 861-864
-
-
Gregor, V.E.1
Emmerling, M.R.2
Lee, C.3
Moore, C.J.4
-
59
-
-
0034036419
-
SAR of 9-amino-1,2,3,4-tetrahydroacridine-based acetylcholinesterase inhibitors: Synthesis, enzyme inhibitory activity, QSAR, and structure-based COMFA of tacrine analogues
-
Recanatini M, Cavalli A, Belluti F, Piazzi L, Rampa A, Bisi A, et al. SAR of 9-amino-1,2,3,4-tetrahydroacridine-based acetylcholinesterase inhibitors: Synthesis, enzyme inhibitory activity, QSAR, and structure-based COMFA of tacrine analogues. J Med Chem 2000; 43: 2007-2018.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 2007-2018
-
-
Recanatini, M.1
Cavalli, A.2
Belluti, F.3
Piazzi, L.4
Rampa, A.5
Bisi, A.6
-
60
-
-
0024338668
-
A practical synthesis of the chinese "nootropic" agent huperzine A: A possible lead in the treatment of Alzheimer's disease
-
Xia Y, Kozikowski AP. A practical synthesis of the chinese "nootropic" agent huperzine A: A possible lead in the treatment of Alzheimer's disease. J Am Chem Soc 1989; 111: 4116-4117.
-
(1989)
J. Am. Chem. Soc.
, vol.111
, pp. 4116-4117
-
-
Xia, Y.1
Kozikowski, A.P.2
-
61
-
-
0024518339
-
A total synthesis of (±)-huperzine A
-
Qian L, Ji R. A total synthesis of (±)-huperzine A. Tetrahedron Lett 1989; 30: 2089-2090.
-
(1989)
Tetrahedron. Lett.
, vol.30
, pp. 2089-2090
-
-
Qian, L.1
Ji, R.2
-
62
-
-
0002004240
-
An enantioselective synthesis of natural (-)-huperzine A via cinchona alkaloidspromoted asymmetric Michael reaction
-
Kaneko S, Yoshino T, Katoh T, Terashima S. An enantioselective synthesis of natural (-)-huperzine A via cinchona alkaloidspromoted asymmetric Michael reaction. Heterocycles 1997; 46: 27-30.
-
(1997)
Heterocycles
, vol.46
, pp. 27-30
-
-
Kaneko, S.1
Yoshino, T.2
Katoh, T.3
Terashima, S.4
-
63
-
-
0025730681
-
Synthesis of huperzine A and its analogues and their anticholinesterase activity
-
Kozikowski AP, Xia Y, Reddy ER, Tückmantel W, Hanin I, Tang XC. Synthesis of huperzine A and its analogues and their anticholinesterase activity. J Org Chem 1991; 56: 4636-4645.
-
(1991)
J. Org. Chem.
, vol.56
, pp. 4636-4645
-
-
Kozikowski, A.P.1
Xia, Y.2
Reddy, E.R.3
Tückmantel, W.4
Hanin, I.5
Tang, X.C.6
-
64
-
-
21144462011
-
Synthesis of analogues of huperzine A
-
He XC, Wang ZY, Li YL, Xu ZR, Bai DL. Synthesis of analogues of huperzine A. Chin Chem Lett 1993; 4: 597-600.
-
(1993)
Chin. Chem. Lett.
, vol.4
, pp. 597-600
-
-
He, X.C.1
Wang, Z.Y.2
Li, Y.L.3
Xu, Z.R.4
Bai, D.L.5
-
65
-
-
0029131257
-
Synthesis and evaluation of 5-amino-5,6,7,8-tetrahydroquino-lines as potential agents for the treatment of Alzheimer's disease
-
Fink DM, Bores GM, Effland RC, Huger FP, Kurys BE, Rush DK, et al. Synthesis and evaluation of 5-amino-5,6,7,8-tetrahydroquino-lines as potential agents for the treatment of Alzheimer's disease. J Med Chem 1995; 38: 3645-3651.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 3645-3651
-
-
Fink, D.M.1
Bores, G.M.2
Effland, R.C.3
Huger, F.P.4
Kurys, B.E.5
Rush, D.K.6
-
66
-
-
0001052820
-
An approach to modified heterocyclic analogues of huperzine A and isohuperzine A. Synthesis of the pyrimidone and pyrazole analogues, and their anticholinesterase activity
-
Kozikowski AP, Campiani G, Nacci V, Sega A, Saxena A, Doctor BP. An approach to modified heterocyclic analogues of huperzine A and isohuperzine A. Synthesis of the pyrimidone and pyrazole analogues, and their anticholinesterase activity. J Chem Soc Perkin Trans I 1996; 1287-1297.
-
(1996)
J. Chem. Soc. Perkin. Trans. I
, pp. 1287-1297
-
-
Kozikowski, A.P.1
Campiani, G.2
Nacci, V.3
Sega, A.4
Saxena, A.5
Doctor, B.P.6
-
67
-
-
0029909228
-
Identification of a more potent analogue of the naturally occurring alkaloid huperzine A. Predictive molecular modelling of its interaction with AChE
-
Kozikowski AP, Campiani G, Sun L-Q, Wang S, Saxena A, Doctor BP. Identification of a more potent analogue of the naturally occurring alkaloid huperzine A. Predictive molecular modelling of its interaction with AChE. J Am Chem Soc 1996; 118: 11357-11362.
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 11357-11362
-
-
Kozikowski, A.P.1
Campiani, G.2
Sun, L.-Q.3
Wang, S.4
Saxena, A.5
Doctor, B.P.6
-
68
-
-
0032474510
-
Synthesis and anticholinesterase activity of huperzine A analogues containing phenol and catechol replacements for the pyridone ring
-
Campiani G, Kozikowski AP, Wang S, Ming L, Nacci V, Saxena A, et al. Synthesis and anticholinesterase activity of huperzine A analogues containing phenol and catechol replacements for the pyridone ring. Bioorg Med Chem Lett 1998; 8: 1413-1418.
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, pp. 1413-1418
-
-
Campiani, G.1
Kozikowski, A.P.2
Wang, S.3
Ming, L.4
Nacci, V.5
Saxena, A.6
-
69
-
-
0033575679
-
Potent, easily synthesized huperzine A-tacrine hybrid acetylcholinesterase inhibitors
-
Carlier PR, Du D-M, Han Y-F, Liu J, Pang Y-P. Potent, easily synthesized huperzine A-tacrine hybrid acetylcholinesterase inhibitors. Bioorg Med Chem Lett 1999; 9: 2335-2338.
-
(1999)
Bioorg. Med. Chem. Lett.
, vol.9
, pp. 2335-2338
-
-
Carlier, P.R.1
Du, D.-M.2
Han, Y.-F.3
Liu, J.4
Pang, Y.-P.5
-
71
-
-
13044253491
-
Synthesis, in vitro pharmacology, and molecular modeling of very potent tacrine-huperzine A hybrids as acetylcholinesterase inhibitors of potential interest for the treatment of Alzheimer's disease
-
Camps P, Achab RE, Görbig DM, Morral J, Muñoz-Torrero D, Badia A, et al. Synthesis, in vitro pharmacology, and molecular modeling of very potent tacrine-huperzine A hybrids as acetylcholinesterase inhibitors of potential interest for the treatment of Alzheimer's disease. J Med Chem 1999; 42: 3227-3242.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 3227-3242
-
-
Camps, P.1
Achab, R.E.2
Görbig, D.M.3
Morral, J.4
Muñoz-Torrero, D.5
Badia, A.6
-
72
-
-
0033966913
-
Huprine X is a novel high-affinity inhibitor of acetylcholinesterase that is of interest for treatment of Alzheimer's disease
-
Camps P, Cusack B, Mallender WD, Achab RE, Morral J, Muñoz-Torrero D, et al. Huprine X is a novel high-affinity inhibitor of acetylcholinesterase that is of interest for treatment of Alzheimer's disease. Mol Pharmacol 2000; 57: 409-417.
-
(2000)
Mol. Pharmacol.
, vol.57
, pp. 409-417
-
-
Camps, P.1
Cusack, B.2
Mallender, W.D.3
Achab, R.E.4
Morral, J.5
Muñoz-Torrero, D.6
-
73
-
-
0037438531
-
Acetylcholinesterase complexed with bivalent ligands related to huperzine A: Experimental evidence for species-dependent protein-ligand complementarity
-
Wong DM, Greenblatt LIM, Dvir H, Carlier PR, Han Y-F, Pang Y-P, et al. Acetylcholinesterase complexed with bivalent ligands related to huperzine A: Experimental evidence for species-dependent protein-ligand complementarity. J Am Chem Soc 2003; 125: 363-373.
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 363-373
-
-
Wong, D.M.1
Greenblatt, L.I.M.2
Dvir, H.3
Carlier, P.R.4
Han, Y.-F.5
Pang, Y.-P.6
-
75
-
-
0031726513
-
Potent acetylcholinesterase inhibitors: Design, synthesis, and structure-activity relationships of bis-interacting ligands in the galanthamine series
-
Mary A, Renko Z, Guillou C, Thal C. Potent acetylcholinesterase inhibitors: Design, synthesis, and structure-activity relationships of bis-interacting ligands in the galanthamine series. Bioorg Med Chem 1998; 6: 1835-1850.
-
(1998)
Bioorg. Med. Chem.
, vol.6
, pp. 1835-1850
-
-
Mary, A.1
Renko, Z.2
Guillou, C.3
Thal, C.4
-
76
-
-
0141704173
-
Update on Alzheimer drugs (galantamine)
-
Raskind MA. Update on Alzheimer drugs (galantamine). Neurologist 2003; 9: 235-240.
-
(2003)
Neurologist
, vol.9
, pp. 235-240
-
-
Raskind, M.A.1
-
77
-
-
0031882851
-
Central nicotinic agonists ABT-418, ABT-089, and (-)-nicotine reduce distractability in adult monkeys
-
Prendergast MA, Jackson WJ, Terry Jr AV, Decker MW, Arneric SP, Buccafusco JJ. Central nicotinic agonists ABT-418, ABT-089, and (-)-nicotine reduce distractability in adult monkeys. Psychopharm 1998; 136: 50-58.
-
(1998)
Psychopharm.
, vol.136
, pp. 50-58
-
-
Prendergast, M.A.1
Jackson, W.J.2
Terry Jr., A.V.3
Decker, M.W.4
Arneric, S.P.5
Buccafusco, J.J.6
-
78
-
-
0034599814
-
Potent acetylcholinesterase inhibitors: Design, synthesis and structure-activity relationships of alkylene linked bis-galanthamine and galanthamine-galanthaminium salts
-
Guillou C, Mary A, Renko DZ, Gras E, Thal C. Potent acetylcholinesterase inhibitors: Design, synthesis and structure-activity relationships of alkylene linked bis-galanthamine and galanthamine-galanthaminium salts. Bioorg Med Chem Lett 2000; 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
-
79
-
-
0032561371
-
Acetylcholinesterase noncovalent inhibitors based on a polyamine backbone for potential use against Alzheimer's disease
-
Melchiorre C, Andrisano V, Bolognesi ML, Budriesi R, Cavalli A, Cavrini V, et al. Acetylcholinesterase noncovalent inhibitors based on a polyamine backbone for potential use against Alzheimer's disease. J Med Chem 1998; 41: 4186-4189.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 4186-4189
-
-
Melchiorre, C.1
Andrisano, V.2
Bolognesi, M.L.3
Budriesi, R.4
Cavalli, A.5
Cavrini, V.6
-
80
-
-
0037435051
-
Structure-activity relationships of acetylcholinesterase noncovalent inhibitors based on a polyamine backbone. 2. Role of the substituents on the phenyl ring and nitrogen atoms of caproctamine
-
Turniatti V, Rosini M, Bartolini M, Cavalli A, Marucci G, Andrisano V, et al. Structure-activity relationships of acetylcholinesterase noncovalent inhibitors based on a polyamine backbone. 2. Role of the substituents on the phenyl ring and nitrogen atoms of caproctamine. J Med Chem 2003; 46: 954-966.
-
(2003)
J. Med. Chem.
, vol.46
, pp. 954-966
-
-
Turniatti, V.1
Rosini, M.2
Bartolini, M.3
Cavalli, A.4
Marucci, G.5
Andrisano, V.6
-
81
-
-
0035382539
-
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. Dynamic deconvolution of a pre-equilibrated dynamic combinatorial library of acetylcholinesterase inhibitors. Chembiochem 2001; 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
-
82
-
-
0037087516
-
Click chemistry in situ: Acetylcholinesterase as a reaction vessel for the selective assembly of a femtomolar inhibitor from an array of building blocks
-
Lewis WG, Green LG, Grynszpan F, Radic Z, Carlier PR, Taylor P, et al. Click chemistry in situ: Acetylcholinesterase as a reaction vessel for the selective assembly of a femtomolar inhibitor from an array of building blocks. Angew Chem Int Ed 2002; 41: 1053-1057.
-
(2002)
Angew Chem. Int. Ed.
, vol.41
, pp. 1053-1057
-
-
Lewis, W.G.1
Green, L.G.2
Grynszpan, F.3
Radic, Z.4
Carlier, P.R.5
Taylor, P.6
-
83
-
-
0000096835
-
Click chemistry: Diverse chemical function from a few good reactions
-
Kolb HC, Finn MG, Sharpless KB. Click chemistry: Diverse chemical function from a few good reactions. Angew Chem Int Ed 2001; 40: 2004.
-
(2001)
Angew Chem. Int. Ed.
, vol.40
, pp. 2004
-
-
Kolb, H.C.1
Finn, M.G.2
Sharpless, K.B.3
-
84
-
-
0348109450
-
The growing impact of click chemistry on drug discovery
-
Kolb HC, Sharpless KB. The growing impact of click chemistry on drug discovery. Drug Discov Today 2003; 8: 1128-1137.
-
(2003)
Drug Discov. Today
, vol.8
, pp. 1128-1137
-
-
Kolb, H.C.1
Sharpless, K.B.2
-
85
-
-
0034648058
-
Protection against ischemic injury in primary cultured mouse astrocytes by bis(7)-tacrine, a novel acetylcholinesterase inhibitor
-
Wu D-C, Xiao X-Q, Ng AKY, Chen PMY, Chung W, Lee NTK, et al. Protection against ischemic injury in primary cultured mouse astrocytes by bis(7)-tacrine, a novel acetylcholinesterase inhibitor. Neurosci Lett 2000; 288: 95-98.
-
(2000)
Neurosci. Lett.
, vol.288
, pp. 95-98
-
-
Wu, D.-C.1
Xiao, X.-Q.2
Ng, A.K.Y.3
Chen, P.M.Y.4
Chung, W.5
Lee, N.T.K.6
-
86
-
-
0034284010
-
Bis(7)-tacrine, a promising anti-Alzheimer's agent, reduces hydrogen-peroxide-induced injury in rat pheochromocytoma cells: Comparison with tacrine
-
Xiao XQ, Lee NT-K, Carlier PR, Pang Y-P, Han YF. Bis(7)-tacrine, a promising anti-Alzheimer's agent, reduces hydrogen-peroxide-induced injury in rat pheochromocytoma cells: Comparison with tacrine. Neurosci Lett 2000; 290: 197-200.
-
(2000)
Neurosci. Lett.
, vol.290
, pp. 197-200
-
-
Xiao, X.Q.1
Lee, N.T.-K.2
Carlier, P.R.3
Pang, Y.-P.4
Han, Y.F.5
-
87
-
-
0037234423
-
The role of acetylcholinesterase in the pathogenesis of Alzheimer's disease
-
Rees TM, Brimijoin S. The role of acetylcholinesterase in the pathogenesis of Alzheimer's disease. Drugs of Today 2003; 39: 75-83.
-
(2003)
Drugs of Today
, vol.39
, pp. 75-83
-
-
Rees, T.M.1
Brimijoin, S.2
-
88
-
-
0037298750
-
β-amyloid aggregation induced by human acetylcholinesterase: Inhibition studies
-
Bartolini M, Bertucci C, Cavrini V, Andrisano V. β-amyloid aggregation induced by human acetylcholinesterase: Inhibition studies. Biochem Pharm 2003; 65: 407-416.
-
(2003)
Biochem. Pharm.
, vol.65
, pp. 407-416
-
-
Bartolini, M.1
Bertucci, C.2
Cavrini, V.3
Andrisano, V.4
-
89
-
-
12444257779
-
3-(4-{[benzyl(methylamino]methyl}-phenyl)-6,7-dimethoxy-2H-2-chromenone (AP2238) inhibits both acetylcholinesterase and acetylcholinesterase-induced β-amyloid aggregation: A dual function lead for Alzheimer's disease therapy
-
Piazzi L, Rampa A, Bisi A, Gobbi S, Belluti F, Cavalli A, et al. 3-(4-{[benzyl(methylamino]methyl}-phenyl)-6,7-dimethoxy-2H-2-chromenone (AP2238) inhibits both acetylcholinesterase and acetylcholinesterase-induced β-amyloid aggregation: A dual function lead for Alzheimer's disease therapy. J Med Chem 2003; 46: 2279-2282.
-
(2003)
J. Med. Chem.
, vol.46
, pp. 2279-2282
-
-
Piazzi, L.1
Rampa, A.2
Bisi, A.3
Gobbi, S.4
Belluti, F.5
Cavalli, A.6
-
90
-
-
0036235070
-
Design and study of piracetam-like nootropics, controversial members of the problematic class of cognition-enhancing drugs
-
Gualtieri F, Manetti D, Romanelli MN, Ghelardini C. Design and study of piracetam-like nootropics, controversial members of the problematic class of cognition-enhancing drugs. Curr Pharm Dgsign 2002; 8(2): 125-38.
-
(2002)
Curr. Pharm. Design
, vol.8
, Issue.2
, pp. 125-138
-
-
Gualtieri, F.1
Manetti, D.2
Romanelli, M.N.3
Ghelardini, C.4
-
91
-
-
0036233946
-
The potential utility of 5-HT1A receptor antagonists in the treatment of cognitive dysfunction associated with Alzheimer s disease
-
Schechter LE, Dawson LA, Harder JA. The potential utility of 5-HT1A receptor antagonists in the treatment of cognitive dysfunction associated with Alzheimer s disease. Curr Pharm Design 2002; 8(2): 139-45.
-
(2002)
Curr. Pharm. Design
, vol.8
, Issue.2
, pp. 139-145
-
-
Schechter, L.E.1
Dawson, L.A.2
Harder, J.A.3
-
92
-
-
0036431821
-
Amyloid forming proteases: Therapeutic targets for Alzheimer's disease
-
Schimmoller F, Higaki JN, Cordell B. Amyloid forming proteases: therapeutic targets for Alzheimer's disease. Curr Pharm Design 2002; 8(28): 2521-31.
-
(2002)
Curr. Pharm. Design
, vol.8
, Issue.28
, pp. 2521-2531
-
-
Schimmoller, F.1
Higaki, J.N.2
Cordell, B.3
|