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10
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0018381173
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Cardiac muscarinic blocking and atropinic blocking effects of a tetramine disulfide with α-adrenoceptor blocking activity
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Benfey, B.G.1
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11
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0018936286
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Potentiation and inhibition of nicotinic effects on striated muscle by the tetramine disulfide benextramine
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12
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0023068542
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2 muscarinic blocking activity as revealed by symmetrical and unsymmetrical poly amines
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14
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15444342741
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Unpublished results
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(b) Unpublished results.
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15
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0024490371
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Structure-activity relationships among methoctramine-related polymethylene tetraamines. Chain-length and substituent effects on M-2 muscarinic receptor blocking activity
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Angeli, P.6
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16
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15444351208
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note
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2O) C, H, N.
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17
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15444354468
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note
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50 values which represent the concentration required to inhibit enzyme activity by 50%.
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18
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15444347907
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note
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3).
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19
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15444349090
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note
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25 Three concentrations of each inhibitor and four substrate concentrations were used; acetylthiocholine concentration never exceeded 0.55 mM, to avoid substrate inhibition. Duplicate assays were conducted at each of the concentration combinations, and the mean of the enzyme velocity values was used for graphical analysis (individual velocity values were all within ±5% of the mean value).
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20
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15444348722
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note
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26 bis-tetrahydroaminacridine inhibitors of AChE. These compounds bind simultaneously at both the catalytic and the peripheral sites of AChE and are characterized by "a linear mixed type of enzyme inhibition".
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21
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15444345220
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note
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28 and retrieved from the Brookhaven Protein Data Bank; Phe330 was replaced by Tyr, which is present in the human AChE, with the same conformation.
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22
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0028081047
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Docking analysis of a series of benzylamino acetylcholinesterase inhibitors with a phthalimide, benzoyl, orindanone moiety
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Yamamoto, Y.; Ishihara, Y.; Kuntz, I. D. Docking analysis of a series of benzylamino acetylcholinesterase inhibitors with a phthalimide, benzoyl, orindanone moiety. J. Med. Chem. 1994, 37, 3141-3153.
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Yamamoto, Y.1
Ishihara, Y.2
Kuntz, I.D.3
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23
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0027368530
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Quaternary ligand binding to aromatic residues in the active-site gorge of acetylcholinesterase
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Harel, M.; Schalk, I.; Ehret-Sabattier, L.; Bouet, F.; Goeldner, M.; Hirth, C.; Axelsen, P.; Silman, I.; Sussman, J. Quaternary ligand binding to aromatic residues in the active-site gorge of acetylcholinesterase. Proc. Natl. Acad. Sci. U.S.A. 1993, 90, 9032-9035.
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Harel, M.1
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Hirth, C.6
Axelsen, P.7
Silman, I.8
Sussman, J.9
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24
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73649209211
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Cumulative dose-response curves. II. Technique for the making of dose-response curves in isolated organs and the evaluation of drug parameters
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Van Rossum, J.M.1
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25
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15444340430
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note
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The backbone atoms of Trp84 and Trp279 from the model and from the structure of AChE cocrystallized with decamethonium (Brookhaven Protein Data Bank entry 1acl) were aligned, and the resulting position of decamethonium is shown in Figure 2.
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26
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33644811612
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A new and rapid colorimetric determination of acetylcholinesterase activity
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Ellmann, G.L.1
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27
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0024205951
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Affinity and selectivity of diperiden enantiomers for muscarinic receptor subtypes
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Eltze, M.1
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29
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0343134441
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Molecular mechanisms for hydrolytic enzyme action. III. A general mechanism for the inhibition of acetylcholinesterase
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Laidler, K.J.2
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30
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0029817834
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Highly potent, selective, and low cost bis-tetrahydroaminacrine inhibitors of acetylcholinesterase
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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.
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Pang, Y.-P.1
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31
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84986437005
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MacroModel - An integrated software system for modeling organic and bioorganic molecules using molecular mechanics
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Mohamadi, F.; Richards, N. G. J.; Guida, W. C.; Liskamp, R. M. J.; Lipton, M. A.; Caulfield, C. E.; Chang, G.; Hendrickson, T. F.; Still, W. C. MacroModel - an integrated software system for modeling organic and bioorganic molecules using molecular mechanics. J. Comput. Chem. 1990, 11, 440-467.
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Still, W.C.9
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32
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0025778840
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Atomic structure of acetylcholinesterase from Torpedo Californica: A prototypic acetylcholine-binding protein
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Sussman, J. L.; 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.
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Sussman, J.L.1
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Toker, L.6
Silman, I.7
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