Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

Demexiptiline

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Demexiptiline
Skeletal formula of demexiptiline
Space-filling model of the demexiptiline molecule
Clinical data
Trade namesDeparon, Tinoran
Routes of
administration
Oral
ATC code
  • none
Legal status
Legal status
  • In general: ℞ (Prescription only)
Pharmacokinetic data
Eliminationhalf-life35 hours[1]
Identifiers
  • 5H-dibenzo(a,d)cyclohepten-5-oneO-(2-(methylamino)ethyl)oxime
CAS Number
PubChemCID
DrugBank
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC18H18N2O
Molar mass278.355 g·mol−1
3D model (JSmol)
  • O(\N=C3/c1ccccc1\C=C/c2c3cccc2)CCNC

Demexiptiline (brand namesDeparon,Tinoran) is atricyclic antidepressant (TCA) used inFrance for the treatment ofdepression.[2][3] It acts primarily as anorepinephrine reuptake inhibitor similarly todesipramine.[4]

Synthesis

[edit]

The ketone dibenzosuberenone (1) is treated withhydroxylamine (2) to give itsketoxime (3). Base-catalyzedalkylation withClCH2CH2NHCH3 (4) yields demexiptiline.[5][6]

References

[edit]
  1. ^Dörwald FZ (4 February 2013).Lead Optimization for Medicinal Chemists: Pharmacokinetic Properties of Functional Groups and Organic Compounds. John Wiley & Sons. pp. 313–.ISBN 978-3-527-64565-7.
  2. ^Swiss Pharmaceutical Society (2000).Index Nominum 2000: International Drug Directory (Book with CD-ROM). Boca Raton: Medpharm Scientific Publishers. p. 301.ISBN 3-88763-075-0.
  3. ^Triggle DJ (1996).Dictionary of Pharmacological Agents. Boca Raton: Chapman & Hall/CRC. p. 583.ISBN 0-412-46630-9.
  4. ^Teste JF, Pelsy-Johann I, Decelle T, Boulu RG (1993). "Anti-immobility activity of different antidepressant drugs using the tail suspension test in normal or reserpinized mice".Fundamental & Clinical Pharmacology.7 (5):219–26.doi:10.1111/j.1472-8206.1993.tb00235.x.PMID 8370568.S2CID 24240307.
  5. ^Aichinger G, Behner O, Hoffmeister F, Schütz S (June 1969). "Basic tricyclic oxyiminoethers and their pharmacological properties".Arzneimittel-Forschung (in German).19: Suppl 5a:838+.PMID 5819763.
  6. ^US 3963778, Schütz S, Behner O, Hoffmeister F, "Basic oximes and their preparation", issued 15 June 1976, assigned to Bayer AG 

Further reading

[edit]
  • Martin A, Masson JM, Jusseaume P, Beloncle M, Voisinet C (November 1981). "[Demexiptiline in the treatment of melancholic states (reflections after 3 years of use)]".Annales médico-psychologiques (in French).139 (9):1023–35.PMID 7337336.
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


Stub icon

Thisdrug article relating to thenervous system is astub. You can help Wikipedia byexpanding it.

Retrieved from "https://en.wikipedia.org/w/index.php?title=Demexiptiline&oldid=1250507899"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp