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Indeloxazine

From Wikipedia, the free encyclopedia
Antidepressant and cerebral activator
Pharmaceutical compound
Indeloxazine
Clinical data
Other namesCI-874, YM-08054
ATC code
  • None
Legal status
Legal status
  • Discontinued
Identifiers
  • 2-(3H-Inden-4-yloxymethyl)morpholine
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC14H17NO2
Molar mass231.295 g·mol−1
3D model (JSmol)
  • O(c1cccc2\C=C/Cc12)CC3OCCNC3
  • InChI=1S/C14H17NO2/c1-3-11-4-2-6-14(13(11)5-1)17-10-12-9-15-7-8-16-12/h1-4,6,12,15H,5,7-10H2 checkY
  • Key:MADRVGBADLFHMO-UHFFFAOYSA-N checkY
  (verify)

Indeloxazine (INN; trade namesElen andNoin) is anantidepressant andcerebral activator[1][2] that was marketed inJapan andSouth Korea byYamanouchi Pharmaceutical Co., Ltd for the treatment ofpsychiatric symptoms associated withcerebrovascular diseases, namelydepression resulting fromstroke,emotional disturbance, andavolition.[3][4] It was marketed from 1988[4] to 1998, when it was removed from the market reportedly for lack of effectiveness.[5]

Indeloxazine acts as aserotonin releasing agent,norepinephrine reuptake inhibitor, andNMDA receptor antagonist.[6][7] It has been found to enhanceacetylcholine release in the ratforebrain through activation of the5-HT4 receptor via its action as a serotonin releasing agent.[8][9][10] The drug has been found to possessnootropic,[11][12]neuroprotective,[13][14][15][16]anticonvulsant,[17] andantidepressant-like effects inanimal models.[1][6]

References

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  1. ^abKojima T, Niigata K, Fujikura T, Tachikawa S, Nozaki Y, Kagami S, Takahashi K (September 1985)."Syntheses of (+/-)-2-[(inden-7-yloxy)methyl]morpholine hydrochloride (YM-08054, indeloxazine hydrochloride) and its derivatives with potential cerebral-activating and antidepressive properties".Chemical & Pharmaceutical Bulletin.33 (9):3766–3774.doi:10.1248/cpb.33.3766.PMID 4092278.
  2. ^Hayes AG, Chang T (January 1983). "Determination of indeloxazine, a new antidepressant agent, in human plasma by gas-liquid chromatography with electron-capture detection".Journal of Chromatography.272 (1):176–180.doi:10.1016/s0378-4347(00)86115-0.PMID 6841538.
  3. ^Index nominum, international drug ... - Google Books. Taylor & Francis. 2000.ISBN 978-3-88763-075-1.
  4. ^abGanellin CR, Triggle JD, MacDonald F (1997).Dictionary of pharmacological agents - Google Books. CRC Press.ISBN 978-0-412-46630-4.
  5. ^Hayashi K, Hashimoto K, Yanagi M, Umeda T, Hama R (August 1998)."Drug approval in Japan questioned".Lancet.352 (9126): 491.doi:10.1016/s0140-6736(05)79232-1.PMID 9708787.S2CID 43687432.
  6. ^abYamaguchi T, Ohyama M, Suzuki M, Ozawa Y, Hatanaka K, Hidaka K, Yamamoto M (September 1998). "Neurochemical and behavioral characterization of potential antidepressant properties of indeloxazine hydrochloride".Neuropharmacology.37 (9):1169–1176.doi:10.1016/s0028-3908(98)00009-4.PMID 9833647.S2CID 12707551.
  7. ^Kaneko S, Sugimura M, Inoue T, Satoh M (June 1991). "Effects of several cerebroprotective drugs on NMDA channel function: evaluation using Xenopus oocytes and [3H]MK-801 binding".European Journal of Pharmacology.207 (2):119–128.doi:10.1016/0922-4106(91)90086-w.PMID 1652446.
  8. ^Peñas-Cazorla R, Vilaró MT (November 2015). "Serotonin 5-HT4 receptors and forebrain cholinergic system: receptor expression in identified cell populations".Brain Structure & Function.220 (6):3413–3434.doi:10.1007/s00429-014-0864-z.hdl:10261/124736.PMID 25183542.S2CID 14116338.
  9. ^Yamaguchi T, Suzuki M, Yamamoto M (December 1997)."Facilitation of acetylcholine release in rat frontal cortex by indeloxazine hydrochloride: involvement of endogenous serotonin and 5-HT4 receptors".Naunyn-Schmiedeberg's Archives of Pharmacology.356 (6):712–720.doi:10.1007/pl00005110.PMID 9453456.S2CID 7800009. Archived fromthe original on 1999-10-08. Retrieved2010-01-11.
  10. ^Yamamoto M, Takahashi K, Ohyama M, Sasamata M, Yatsugi S, Okada M, Endoh H (May 1994). "Possible involvement of central cholinergic system in ameliorating effects of indeloxazine, a cerebral activator, on disturbance of learning behavior in rats".Progress in Neuro-Psychopharmacology & Biological Psychiatry.18 (3):603–613.doi:10.1016/0278-5846(94)90016-7.PMID 8078992.S2CID 11703415.
  11. ^Ogawa N, Haba K, Sora YH, Higashida A, Sato H, Ogawa S (1988). "Comparison of the effects of bifemelane hydrochloride and indeloxazine hydrochloride on scopolamine hydrobromide-induced impairment in radial maze performance".Clinical Therapeutics.10 (6):704–711.PMID 3219685.
  12. ^Yamamoto M, Shimizu M (July 1987). "Cerebral activating properties of indeloxazine hydrochloride".Neuropharmacology.26 (7A):761–770.doi:10.1016/0028-3908(87)90239-5.PMID 3627384.S2CID 46153252.
  13. ^Ogawa N, Haba K, Yoshikawa H, Ono T, Mizukawa K (August 1988). "Comparison of the effects of bifemelane hydrochloride, idebenone and indeloxazine hydrochloride on ischemia-induced depletion of brain acetylcholine levels in gerbils".Research Communications in Chemical Pathology and Pharmacology.61 (2):285–288.PMID 3187197.
  14. ^Yamamoto M, Shimizu M, Sakamoto N, Ohtomo H, Kogure K (November 1987). "Protective effects of indeloxazine hydrochloride on cerebral ischemia in animals".Archives Internationales de Pharmacodynamie et de Therapie.290 (1):16–24.PMID 3446040.
  15. ^Shimizu-Sasamata M, Terai M, Harada M, Yamamoto M (1993). "Anti-hypoxic and anti-ischemic actions of indeloxazine hydrochloride and its optical isomers: possible involvement of cerebral energy metabolism".Archives Internationales de Pharmacodynamie et de Therapie.324:33–46.PMID 8297184.
  16. ^Yamamoto M, Shimizu M (April 1987). "Effects of indeloxazine hydrochloride (YM-08054) on anoxia".Archives Internationales de Pharmacodynamie et de Therapie.286 (2):272–281.PMID 3592867.
  17. ^Nakamura J, Anraku T, Shirouzu M, Iwashita Y, Nakazawa Y (June 1993). "Effects of indeloxazine HCl on kindled amygdaloid seizures in rats: comparison with the effects of phenytoin, diazepam, ethanol, and imipramine".Pharmacology, Biochemistry, and Behavior.45 (2):445–450.doi:10.1016/0091-3057(93)90263-s.PMID 8327550.S2CID 26761718.
SSRIsTooltip Selective serotonin reuptake inhibitors
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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
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Non-selective
MAOATooltip Monoamine oxidase A-selective
MAOBTooltip Monoamine oxidase B-selective
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AMPARTooltip α-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor
KARTooltip Kainate receptor
NMDARTooltip N-Methyl-D-aspartate receptor
Group I
mGluR1Tooltip Metabotropic glutamate receptor 1
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mGluR2Tooltip Metabotropic glutamate receptor 2
mGluR3Tooltip Metabotropic glutamate receptor 3
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mGluR4Tooltip Metabotropic glutamate receptor 4
mGluR6Tooltip Metabotropic glutamate receptor 6
mGluR7Tooltip Metabotropic glutamate receptor 7
mGluR8Tooltip Metabotropic glutamate receptor 8
DRAsTooltip Dopamine releasing agents
NRAsTooltip Norepinephrine releasing agents
SRAsTooltip Serotonin releasing agents
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