Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

Butanserin

From Wikipedia, the free encyclopedia
Pharmaceutical compound
Butanserin
Clinical data
Other namesR-53393; R53393; R-53,393
Drug classSerotonin 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
PubChemCID
DrugBank
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC24H26FN3O3
Molar mass423.488 g·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 (INNTooltip International Nonproprietary Name; developmental code nameR-53393) is aserotonin5-HT2 receptorantagonist andα1-adrenergic receptor antagonist which was studied as anantihypertensive agent but was never marketed.[1][2][3] It was first described in thescientific literature by 1984.[1][2][3]

See also

[edit]

References

[edit]
  1. ^abElks, J. (14 November 2014).The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer.ISBN 978-1-4757-2085-3. Retrieved16 January 2026.
  2. ^abMegens 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. ^abKorstanje 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.
5-HT1
5-HT1A
5-HT1B
5-HT1D
5-HT1E
5-HT1F
5-HT2
5-HT2A
5-HT2B
5-HT2C
5-HT37
5-HT3
5-HT4
5-HT5A
5-HT6
5-HT7
α1
Agonists
Antagonists
α2
Agonists
Antagonists
β
Agonists
Antagonists
Stub icon

Thisdrug article relating to thecardiovascular system is astub. You can help Wikipedia byadding missing information.

Retrieved from "https://en.wikipedia.org/w/index.php?title=Butanserin&oldid=1334186565"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2026 Movatter.jp