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Butanserin

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Pharmaceutical compound
Butanserin
Clinical data
Other namesR-53393; R53393; R-53,393
Drug class Serotonin 5-HT2A receptor antagonist; α1-Adrenergic receptor antagonist; Antihypertensive agent
ATC code
  • None
Identifiers
  • 3-[4-[4-(4-fluorobenzoyl)piperidin-1-yl]butyl]-1H-quinazoline-2,4-dione
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
Formula C24H26FN3O3
Molar mass 423.488g·mol−1
3D model (JSmol)
  • C1CN(CCC1C(=O)C2=CC=C(C=C2)F)CCCCN3C(=O)C4=CC=CC=C4NC3=O
  • InChI=1S/C24H26FN3O3/c25-19-9-7-17(8-10-19)22(29)18-11-15-27(16-12-18)13-3-4-14-28-23(30)20-5-1-2-6-21(20)26-24(28)31/h1-2,5-10,18H,3-4,11-16H2,(H,26,31)
  • Key:MLDQSYUQSLUEPG-UHFFFAOYSA-N

Butanserin (INN Tooltip International Nonproprietary Name; developmental code name R-53393) is a serotonin 5-HT2 receptor antagonist and α1-adrenergic receptor antagonist which was studied as an antihypertensive agent but was never marketed.[1] [2] [3] It was first described in the scientific literature by 1984.[1] [2] [3]

See also

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References

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  1. 1 2 Elks, J. (14 November 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. ISBN 978-1-4757-2085-3 . Retrieved 16 January 2026.
  2. 1 2 Megens AA, Niemegeers CJ (August 1984). "Antagonism of the antidiarrhoeal effect of clonidine and the lethal effect of noradrenaline in rats: a reliable procedure to evaluate the in-vivo alpha 1- and alpha 2-blocking activity of drugs?". J Pharm Pharmacol. 36 (8): 516–520. doi:10.1111/j.2042-7158.1984.tb04442.x. PMID 6148393.
  3. 1 2 Korstanje C, Sprenkels R, Doods HN, Hugtenburg JG, Boddeke E, Batink HD, Thoolen MJ, Van Zwieten PA (May 1986). "Characterization of flufylline, fluprofylline, ritanserin, butanserin and R 56413 with respect to in-vivo alpha 1-,alpha 2- and 5-HT2-receptor antagonism and in-vitro affinity for alpha 1-,alpha 2- and 5-HT2-receptors: comparison with ketanserin". J Pharm Pharmacol. 38 (5): 374–379. doi:10.1111/j.2042-7158.1986.tb04590.x. PMID 2872314.
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