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Varenicline: An α4β2 Nicotinic Receptor Partial Agonist for Smoking Cessation
Journal of Medicinal Chemistry · 2005 · Vol. 48(10) · pp. 3474–3477
Jotham W. Coe✉(Pfizer (United States))Paige R. Brooks(Pfizer (United States))Michael G. Vetelino(Pfizer (United States))Michael Wirtz(Pfizer (United States))Eric P. Arnold(Pfizer (United States))Jianhua Huang(Pfizer (United States))Steven B. Sands(Pfizer (United States))Thomas I. Davis(Pfizer (United States))Lorraine A. Lebel(Pfizer (United States))Carol B. Fox(Pfizer (United States))Alka Shrikhande(Pfizer (United States))James Heym(Pfizer (United States))Eric Schaeffer(Pfizer (United States))Hans Rollema(Pfizer (United States))Yi Lu(Pfizer (United States))Robert S. Mansbach(Pfizer (United States))Leslie K. Chambers(Pfizer (United States))Charles C. Rovetti(Pfizer (United States))David W. Schulz(Pfizer (United States))F. David Tingley(Pfizer (United States))Brian T. O’Neill(Pfizer (United States))
Abstract
Herein we describe a novel series of compounds from which varenicline (1, 6,7,8,9-tetrahydro-6,10-methano-6H-pyrazino[2,3-h][3]benzazepine) has been identified for smoking cessation. Neuronal nicotinic acetylcholine receptors (nAChRs) mediate the dependence-producing effects of nicotine. We have pursued alpha4beta2 nicotinic receptor partial agonists to inhibit dopaminergic activation produced by smoking while simultaneously providing relief from the craving and withdrawal syndrome that accompanies cessation attempts. Varenicline displays high alpha4beta2 nAChR affinity and the desired in vivo dopaminergic profile.
Nicotinic Acetylcholine Receptors StudyReceptor Mechanisms and SignalingSynthesis and Biological EvaluationVareniclinePartial agonistChemistryNicotinic agonistSmoking cessationNicotinePharmacologyAgonistNicotinic acetylcholine receptorAcetylcholine receptor
MeSH terms
VareniclineAnimalsBenzazepinesCell LineCerebral CortexHumansOocytesQuinoxalinesRadioligand AssayReceptors, NicotinicXenopus laevisSmoking CessationNicotinic AgonistsRatsIn Vitro Techniques
Citations
930
FWCI
22.07
field-weighted impact
References
72
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100%
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BMJ · 1994 · 5,770 citations
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