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SC-53116: The First Selective Agonist at the Newly Identified Serotonin 5-HT4 Receptor Subtype
Journal of Medicinal Chemistry
  • Daniel L. Flynn
  • Daniel Zabrowski
  • Daniel Becker, Loyola University Chicago
  • Roger Nosal
Document Type
Article
Publication Date
3-1-1992
Pages
1486–1489
Publisher Name
American Chemical Society
Disciplines
Abstract

Serotonin acts as a neurotransmitter, neuromodulator, and hormone in mammals, and it is known to exhibit profound pharmacological activities in the central nervous system, autonomic nervous system, enteric nervous system, and cardiovascular system. Among monoamine neuro-transmitters, serotonin is unsurpassed in the number of receptor subtypes identified. Until recently, serotonin was thought to act through receptors subtyped as 5-HT1, 5-HT2, and 5-HT3. Furthermore, even these subtypes have been subclassed to now include 5-HT1A, 5-HT1B, 5-HTlc, 5-HT1D, 5-HT2A, 5-HT2B, and 5-HT3A ,5-HT3B ,and 5-HT33C.2

Comments
Author Posting © American Chemical Society, 1992. The definitive version was published in Journal of Medicinal Chemistry, Volume 35, Number 8, April 1992. http://dx.doi.org/10.1021/jm00086a019
Creative Commons License
Creative Commons Attribution-Noncommercial-No Derivative Works 3.0
Citation Information
Daniel L. Flynn, Daniel Zabrowski, Daniel Becker and Roger Nosal. "SC-53116: The First Selective Agonist at the Newly Identified Serotonin 5-HT4 Receptor Subtype" Journal of Medicinal Chemistry Vol. 35 Iss. 8 (1992)
Available at: http://works.bepress.com/daniel_p_becker/12/