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Pipoxizine

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Pipoxizine
Clinical data
ATC code
  • None
Identifiers
  • 2-(2-{2-[4-(Diphenylmethylene)-1-piperidinyl]ethoxy}ethoxy)ethanol
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC24H31NO3
Molar mass381.516 g·mol−1
3D model (JSmol)
  • c1ccc(cc1)C(=C2CCN(CC2)CCOCCOCCO)c3ccccc3
  • InChI=1S/C24H31NO3/c26-16-18-28-20-19-27-17-15-25-13-11-23(12-14-25)24(21-7-3-1-4-8-21)22-9-5-2-6-10-22/h1-10,26H,11-20H2
  • Key:SCMPXORBOTWFTI-UHFFFAOYSA-N

Pipoxizine (INNTooltip International Nonproprietary Name) is afirst-generation antihistamine as well asserotonin antagonist of thediphenylmethylpiperazine group related tohydroxyzine.[1][2] It was investigated as abronchodilator but was never marketed.[1][3][4]

References

[edit]
  1. ^abGanellin CR, Triggle DJ (21 November 1996).Dictionary of Pharmacological Agents. CRC Press. pp. 1619–.ISBN 978-0-412-46630-4.
  2. ^World Health Organization (1988).International Nonproprietary Names (INN) for Pharmaceutical Substances. W.H.O.ISBN 9789240560369.
  3. ^Brunner A, Gartmann J, Studler H. "Pipoxizine, a New Bronchodilator".Lung.154 (2): 143.
  4. ^Neukirch F, Korobaeff M, Verdier F, Timsit G, Fay M, Drutel P (1978). "[Effect of a histamine aerosol in 20 subjects with histamine hyperreactivity. Application to a study of the protective properties of pipoxizine]".Revue de l'Institut d'Hygiene des Mines (in French).33 (4):191–195.PMID 45187.
H1
Agonists
Antagonists
H2
Agonists
Antagonists
H3
Agonists
Antagonists
H4
Agonists
Antagonists
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
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