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Oxypertine

From Wikipedia, the free encyclopedia
Antipsychotic medication

Pharmaceutical compound
Oxypertine
Clinical data
Trade namesOxypertine, others
Other namesWIN-18501; WIN18501; WIN-18,501, Win-18501; Win-18501-2
AHFS/Drugs.comInternational Drug Names
Routes of
administration		By mouth
ATC code
Legal status
Legal status
  • BR: Class C1 (Other controlled substances)[1]
  • In general: ℞ (Prescription only)
Identifiers
  • 5,6-Dimethoxy-2-methyl-3-[2-(4-phenylpiperazin-1-yl)ethyl]-1H-indole
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
CompTox Dashboard(EPA)
ECHA InfoCard100.005.291Edit this at Wikidata
Chemical and physical data
FormulaC23H29N3O2
Molar mass379.504 g·mol−1
3D model (JSmol)
  • CC1=C(C2=CC(=C(C=C2N1)OC)OC)CCN3CCN(CC3)C4=CC=CC=C4
  • InChI=1S/C23H29N3O2/c1-17-19(20-15-22(27-2)23(28-3)16-21(20)24-17)9-10-25-11-13-26(14-12-25)18-7-5-4-6-8-18/h4-8,15-16,24H,9-14H2,1-3H3 ☒N
  • Key:XCWPUUGSGHNIDZ-UHFFFAOYSA-N ☒N
  (verify)

Oxypertine, sold under the brand nameOxypertine among others, is anantipsychoticmedication of thepertine group which was previously used in the treatment ofschizophrenia but is no longer marketed.[2] It was also evaluated for the treatment ofanxiety.[3]

Pharmacology

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Pharmacodynamics

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The drug shows highaffinity for theserotonin5-HT2 anddopamineD2 receptors (Ki = 8.6 nM and 30 nM, respectively).[4] It antagonizes the behavioral effects oftryptamine, aserotonin receptoragonist, andapomorphine, adopamine receptoragonist, in animals.[4][5] Likereserpine andtetrabenazine, oxypertine depletescatecholamines, though notserotonin, possibly contributing to its antipsychotic effectiveness.[6]

Chemistry

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Chemically, it is asubstituted tryptamine andphenylpiperazinederivative.[7] Itschemical structure is similar to other "pertines" includingalpertine,milipertine, andsolypertine.[8][9]

History

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Oxypertine was first described in thescientific literature by 1962.[10]

Society and culture

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Names

[edit]

Oxypertine is thegeneric name of the drug and itsINNTooltip International Nonproprietary Name,USANTooltip United States Adopted Name,BANTooltip British Approved Name,DCFTooltip Dénomination Commune Française, andJANTooltip Japanese Accepted Name.[10][11][12][13] It is also known by its former developmental code nameWIN-18501.[10][11][12][13] The drug has been sold under brand names includingEquipertine,Forit,Integrin,Lanturil,Lotawin,Opertil, andOxypertine.[10][11][12][13]

See also

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References

[edit]
  1. ^Anvisa (2023-03-31)."RDC Nº 784 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial" [Collegiate Board Resolution No. 784 - Lists of Narcotic, Psychotropic, Precursor, and Other Substances under Special Control] (in Brazilian Portuguese).Diário Oficial da União (published 2023-04-04).Archived from the original on 2023-08-03. Retrieved2023-08-16.
  2. ^Hall C, Rhodes PH (1996).Dictionary of organic compounds. London: Chapman & Hall.ISBN 0-412-54090-8.
  3. ^Somohano MD, Broissin MC, Sobrino ZA (1976). "[Clinical evaluation of oxypertine in anxiety conditions]".Neurologia, Neurocirugia, Psiquiatria (in Spanish).17 (3):171–180.PMID 12484.
  4. ^abMegens AA, Kennis LE (1996). "Risperidone and related 5HT2/D2 antagonists: a new type of antipsychotic agent?". Progress in Medicinal Chemistry.33:185–232.doi:10.1016/s0079-6468(08)70306-0.ISBN 978-0-444-82310-6.PMID 8776944.{{cite journal}}:Cite journal requires|journal= (help)
  5. ^Niemegeers CJ, Janssen PA (June 1979). "A systematic study of the pharmacological activities of dopamine antagonists".Life Sciences.24 (24). Elsevier BV:2201–2216.doi:10.1016/0024-3205(79)90096-1.PMID 388130.
  6. ^Bak IJ, Hassler R, Kim JS (1969). "Differential monoamine depletion by oxypertine in nerve terminals. Granulated synaptic vesicles in relation to depletion of norepinephrine, dopamine and serotonin".Zeitschrift für Zellforschung und Mikroskopische Anatomie.101 (3):448–462.doi:10.1007/BF00335580.PMID 5362847.S2CID 32583722.
  7. ^Breulet M, Labar P, Delree C, Collard J, Bobon J (February 1968). "[Oxypertine, peperazine derivative of tryptophan with neuroleptic and dynamogenic properties]".Acta Neurologica et Psychiatrica Belgica (in French).68 (2):116–127.PMID 4972600.
  8. ^Ellis GP, Luscombe DK (1996).Progress in Medicinal Chemistry. Elsevier Science. p. 219.ISBN 978-0-08-086281-1. Retrieved30 October 2024.Pertines (class 7; Table 5.12) The pertines oxypertine, solypertine, milipertine, and alpertine are piperazinylethylindoles.
  9. ^Lednicer D, Mitscher LA (1980).The Organic Chemistry of Drug Synthesis, Volume 2. Organic Chemistry Series of Drug Synthesis. Wiley. pp. 341–343.ISBN 978-0-471-04392-8. Retrieved30 October 2024.
  10. ^abcdElks J (2014).The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer US. p. 924.ISBN 978-1-4757-2085-3. Retrieved2 November 2024.
  11. ^abcSchweizerischer Apotheker-Verein (2000).Index Nominum 2000: International Drug Directory. Medpharm Scientific Publishers. p. 779.ISBN 978-3-88763-075-1. Retrieved2 November 2024.
  12. ^abcMorton IK, Hall JM (2012).Concise Dictionary of Pharmacological Agents: Properties and Synonyms. Springer Netherlands. p. 212.ISBN 978-94-011-4439-1. Retrieved2 November 2024.
  13. ^abc"List of Antipsychotics". Archived fromthe original on 2016-03-03.


Typical
Disputed
Atypical
Others
D1-like
Agonists
PAMs
Antagonists
D2-like
Agonists
Antagonists
5-HT1
5-HT1A
5-HT1B
5-HT1D
5-HT1E
5-HT1F
5-HT2
5-HT2A
5-HT2B
5-HT2C
5-HT3–7
5-HT3
5-HT4
5-HT5A
5-HT6
5-HT7
Tryptamines
4-Hydroxytryptamines
andesters/ethers
5-Hydroxy- and
5-methoxytryptamines
N-Acetyltryptamines
α-Alkyltryptamines
Cyclized tryptamines
Isotryptamines
Related compounds
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