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Quinupramine

From Wikipedia, the free encyclopedia
Tricyclic antidepressant
Pharmaceutical compound
Quinupramine
Clinical data
Routes of
administration
Oral
ATC code
Legal status
Legal status
  • In general: ℞ (Prescription only)
Pharmacokinetic data
Eliminationhalf-life33 hours
Identifiers
  • (±)-11-quinuclidin-3-yl-5,6-dihydrobenzo[b][1]benzazepine
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
CompTox Dashboard(EPA)
ECHA InfoCard100.046.149Edit this at Wikidata
Chemical and physical data
FormulaC21H24N2
Molar mass304.437 g·mol−1

Quinupramine (brand namesKevopril,Kinupril,Adeprim,Quinuprine) is atricyclic antidepressant (TCA) used inEurope for the treatment ofdepression.[1][2]

Pharmacologically, quinupramine actsin vitro as a strongmuscarinic acetylcholine receptorantagonist (anticholinergic) andH1 receptorantagonist (antihistamine), moderate5-HT2 receptorantagonist, and weakserotonin andnorepinephrine reuptake inhibitor.[3] It has negligible affinity for theα1-adrenergic,α2-adrenergic,β-adrenergic, orD2receptor.[3]

Clinically, quinupramine is reported to bestimulating similarly toimipramine,desipramine, anddemexiptiline.[4] It can be inferred that itsin vivometabolites may have stronger effects on the reuptake of norepinephrine and/or serotonin than quinupramine itself.[citation needed]

References

[edit]
  1. ^Swiss Pharmaceutical Society (2000).Index Nominum 2000: International Drug Directory (Book with CD-ROM). Boca Raton: Medpharm Scientific Publishers. p. 908.ISBN 3-88763-075-0.
  2. ^Vela JM, Buschmann H, Holenz J, Párraga A, Torrens A (2007).Antidepressants, Antipsychotics, Anxiolytics: From Chemistry and Pharmacology to Clinical Application. Weinheim: Wiley-VCH. p. 248.ISBN 978-3-527-31058-6.
  3. ^abSakamoto H, Yokoyama N, Kohno S, Ohata K (December 1984)."Receptor binding profile of quinupramine, a new tricyclic antidepressant".Japanese Journal of Pharmacology.36 (4):455–460.doi:10.1254/jjp.36.455.PMID 6098759.
  4. ^Kent A, Billiard M (2003).Sleep: physiology, investigations, and medicine. New York: Kluwer Academic/Plenum. p. 233.ISBN 0-306-47406-9.
SSRIsTooltip Selective serotonin reuptake inhibitors
SNRIsTooltip Serotonin–norepinephrine reuptake inhibitors
NRIsTooltip Norepinephrine reuptake inhibitors
NDRIsTooltip Norepinephrine–dopamine reuptake inhibitors
NaSSAsTooltip Noradrenergic and specific serotonergic antidepressants
SARIsTooltip Serotonin antagonist and reuptake inhibitors
SMSTooltip Serotonin modulator and stimulators
Others
TCAsTooltip Tricyclic antidepressants
TeCAsTooltip Tetracyclic antidepressants
Others
Non-selective
MAOATooltip Monoamine oxidase A-selective
MAOBTooltip Monoamine oxidase B-selective
Miscellaneous
α1
Agonists
Antagonists
α2
Agonists
Antagonists
β
Agonists
Antagonists
H1
Agonists
Antagonists
H2
Agonists
Antagonists
H3
Agonists
Antagonists
H4
Agonists
Antagonists
DATTooltip Dopamine transporter
(DRIsTooltip Dopamine reuptake inhibitors)
NETTooltip Norepinephrine transporter
(NRIsTooltip Norepinephrine reuptake inhibitors)
SERTTooltip Serotonin transporter
(SRIsTooltip Serotonin reuptake inhibitors)
VMATsTooltip Vesicular monoamine transporters
Others
mAChRsTooltip Muscarinic acetylcholine receptors
Agonists
Antagonists
Precursors
(andprodrugs)
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
Classes
Antidepressants
(Tricyclic antidepressants(TCAs))
Antihistamines
Antipsychotics
Anticonvulsants
Anticholinergics
Others
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