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Ketipramine

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Ketipramine
Clinical data
Routes of
administration
Oral
ATC code
  • none
Identifiers
  • 5-[3-(dimethylamino)propyl]-5,11-dihydro-10H-dibenzo[b,f]azepin-10-one
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC19H22N2O
Molar mass294.398 g·mol−1
3D model (JSmol)
  • O=C3c1c(cccc1)N(c2c(cccc2)C3)CCCN(C)C

Ketipramine (G-35,259), also known asketimipramine orketoimipramine, is atricyclic antidepressant (TCA) that was tested inclinical trials for the treatment ofdepression in the 1960s but was never marketed.[1][2][3] It differs fromimipramine in terms ofchemical structure only by a singleketonegroup, and is approximately equivalent in effectiveness as anantidepressant in comparison.[4]

It was one of the drugs tested byRoland Kuhn in a series of unethical experiments testing drugs on children withoutinformed consent that were done in a psychiatric hospital located in Münsterlingen,Switzerland.[5][6][7]

See also

[edit]

References

[edit]
  1. ^Dictionary of organic compounds. London: Chapman & Hall. 1996.ISBN 0-412-54090-8.
  2. ^Simeon J, Fuchs M, Nikolovski O, Bucci L (1970)."Ketipramine in the therapy of depression in outpatients".Psychosomatics.11 (4):342–6.doi:10.1016/S0033-3182(70)71634-4.PMID 5459338. Archived fromthe original on 2011-07-27.
  3. ^Park S, Glick B, Floyd A, Gershon S (May 1971). "Ketipramine fumarate as compared to imipramine in depressed outpatients".Current Therapeutic Research, Clinical and Experimental.13 (5):322–5.PMID 4998396.
  4. ^Author Unknown (1971).Ann Reports Medicinal Chem V6 (v. 6). Boston: Academic Press.ISBN 0-12-040506-7.{{cite book}}:|author= has generic name (help)
  5. ^Die Experimente von Münsterlingen 20. November 2012. Tages-Anzeiger
  6. ^Münsterlingen: Alles noch viel schlimmer
  7. ^Simone Rau:Das Ausmass der Medi-Versuche in Münsterlingen ist weit grösser. In:Der Bund, 31. Oktober 2016.
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
5-HT1ARTooltip 5-HT1A receptoragonists
GABAARTooltip GABAA receptorPAMsTooltip positive allosteric modulators
Hypnotics
Gabapentinoids
(α2δVDCCblockers)
Antidepressants
Antipsychotics
Sympatholytics
(Antiadrenergics)
Others
α1
Agonists
Antagonists
α2
Agonists
Antagonists
β
Agonists
Antagonists
mAChRsTooltip Muscarinic acetylcholine receptors
Agonists
Antagonists
Precursors
(andprodrugs)
nAChRsTooltip Nicotinic acetylcholine receptors
Agonists
(andPAMsTooltip positive allosteric modulators)
Antagonists
(andNAMsTooltip negative allosteric modulators)
Precursors
(andprodrugs)
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
Classes
Antidepressants
(Tricyclic antidepressants(TCAs))
Antihistamines
Antipsychotics
Anticonvulsants
Anticholinergics
Others
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