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Lin, N.-H.; Gunn, D. E.; Ryther, K. B.; Garvey, D. S.; Donnelly-Roberts, D. L.; Decker, M. W.; Brioni, J. D.; Buckley, M. J.; Rodrigues, A. D.; Marsh, K. G.; Anderson, D. J.; Buccaftisco, J. J.; Prendergast, M. A.; Sullivan, J. P.; Williams, M.; Arneric, S. P.; Holladay, M. W. Structure-activity studies on 2-methyl-3-(2(S)-pyrrolidinylmethoxy)pyridine (ABT-089): an orally bioavailable 3-pyridyl ether nicotinic acetylcholine receptor ligand with cognition-enhancing properties. J. Med. Chem. 1997, 40, 385-390.
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D values reported in the literature. Ebnöther, A.; Weber, H. P.; Meier, W. Helv. Chim. Acta 1976, 59, 2462-2468.
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24
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85066772083
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note
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The isomers were analyzed by normal-phase HPLC with a Daicel Chiralpak AD column (10 mm, 250 × 4.6 mm) at room temperature, using a mobile phase consisting of heptane, ethanol, and trifluoroacetic acid (90:10:0.2) at 1.0 mL/min. Detection was carried out at 254 nm.
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25
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15144343126
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Characterization of human recombinant neuronal nicotinic acetylcholine receptor subunit combinations α2β4, α3β4 and α4β4 stably expressed in HEK293 cells
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(a) Stauderman, K. A.; Mahaffy, L. S.; Akong, M.; Veliçelebi, G.; Chavez-Noriega, L. E.; Crona, J. H.; Johnson, E. C.; Elliott, K. J.; Gillespie, A.; Reid, R. T.; Adams, P.; Harpold, M. M.; Corey-Naeve, J. Characterization of human recombinant neuronal nicotinic acetylcholine receptor subunit combinations α2β4, α3β4 and α4β4 stably expressed in HEK293 cells. J. Pharmacol. Exp. Ther. 1998, 284, 777-789.
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26
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85066772818
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note
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Compound 5 was tested at a saturated concentration with current responses (elicited at -60 mV) normalized to the response produced by a saturating concentration of nicotine (for α2β4, α3β4, α4β2, and α4β4), acetylcholine (α2β2 and α7), and DMPP (α3β2) applied to the same oocytes.
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27
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0030941561
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Pharmacological characterization of recombinant human neuronal nicotinic acetylcholine receptors hα2β2, hα2β4, hα3β2, hα3β4, hα4β2, hα4β4 and hα7 expressed in Xenopus oocytes
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Chavez-Noriega, L. E.; Crona, J. H.; Washburn, M. S.; Urrutia, A.; Elliott, K. J.; Johnson, E. C. Pharmacological characterization of recombinant human neuronal nicotinic acetylcholine receptors hα2β2, hα2β4, hα3β2, hα3β4, hα4β2, hα4β4 and hα7 expressed in Xenopus oocytes. J. Pharmacol. Exp. Ther. 1997, 280, 346-456.
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28
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0142097347
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Electrophysiological characterization of SIB-1553A activity on recombinant human nicotinic receptors express in Xenopus oocytes and HEK-293 cells
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Washburn, M. S.; Chavez-Noriega, L. E.; Crona, J. H.; Vernier, J.-M.; Johnson, E. Electrophysiological characterization of SIB-1553A activity on recombinant human nicotinic receptors express in Xenopus oocytes and HEK-293 cells. Soc. Neurosci. Abstr. 1997, 23, 1198.
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A subtype of nicotinic cholinergic receptor in rat brain is composed of α4 and β2 subunits and is up-regulated by chronic nicotine treatment
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Pharmacological characterization of SIB-1553A, a novel subtype selective neuronal nicotinic acetylcholine receptor agonist
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SIB-1553A, a novel nAChR agonist with cognitive enhancing properties in aged rodents and nonhuman primates: Effects on various memory forms
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Bontempi, B.; Whelan, K. T.; Risbrough, V. B.; Joppa, M. A.; Kille, N.; Buccafusco, J. J.; Menzaghi, F.; Lloyd, G. K. SIB-1553A, a novel nAChR agonist with cognitive enhancing properties in aged rodents and nonhuman primates: effects on various memory forms. Soc. Neurosci. Abstr. 1997, 23, 477.15.
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