Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

Gevotroline

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Gevotroline
Clinical data
Routes of
administration
Oral
ATC code
  • None
Legal status
Legal status
  • In general: uncontrolled
Identifiers
  • 8-fluoro-2-(3-pyridin-3-ylpropyl)-1,3,4,5-tetrahydropyrido[4,3-b]indole
CAS Number
PubChemCID
ChemSpider
UNII
ChEBI
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC19H20FN3
Molar mass309.388 g·mol−1
3D model (JSmol)
  • Fc2cc1c3c([nH]c1cc2)CCN(C3)CCCc4cccnc4

Gevotroline (WY-47,384) is anatypical antipsychotic with atricyclicstructure which was under development for the treatment ofschizophrenia byWyeth-Ayerst.[1][2][3] It acts as a balanced, modestaffinityD2 and5-HT2 receptorantagonist and also possesses highaffinity for thesigma receptor.[2][4][5][6] It was well tolerated and showed efficacy inphase IIclinical trials but was never marketed.[2][3]

See also

[edit]

References

[edit]
  1. ^Triggle DJ (1996).Dictionary of Pharmacological Agents. Boca Raton: Chapman & Hall/CRC.ISBN 0-412-46630-9.
  2. ^abcAbou-Gharbia M, Moyer JA (1990). Bristol JA (ed.)."Novel Antipyschotic Agents".Annual Reports in Medicinal Chemistry.25. Boston: Academic Press:1–10.doi:10.1016/S0065-7743(08)61577-8.ISBN 0-12-040525-3.
  3. ^abJackson DM, Mohell N (1996)."A Review of the Pharmacology of New Antipsychotic Drugs". In Stone TW (ed.).CNS neurotransmitters and neuromodulators: dopamine. Boca Raton: CRC Press.ISBN 0-8493-7632-7.
  4. ^Snyder SH, Largent BL (1989). "Receptor mechanisms in antipsychotic drug action: focus on sigma receptors".The Journal of Neuropsychiatry and Clinical Neurosciences.1 (1):7–15.doi:10.1176/jnp.1.1.7.PMID 2577720.
  5. ^Matheson GK, Guthrie D, Bauer C, Knowles A, White G, Ruston C (January 1991). "Sigma receptor ligands alter concentrations of corticosterone in plasma in the rat".Neuropharmacology.30 (1):79–87.doi:10.1016/0028-3908(91)90046-E.PMID 1675451.S2CID 29702968.
  6. ^Gudelsky GA, Nash JF (February 1992). "Neuroendocrinological and neurochemical effects of sigma ligands".Neuropharmacology.31 (2):157–162.doi:10.1016/0028-3908(92)90026-L.PMID 1348112.S2CID 36585024.
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-HT37
5-HT3
5-HT4
5-HT5A
5-HT6
5-HT7
σ1
σ2
Unsorted
Classes
Antidepressants
(Tricyclic antidepressants(TCAs))
Antihistamines
Antipsychotics
Anticonvulsants
Anticholinergics
Others
Retrieved from "https://en.wikipedia.org/w/index.php?title=Gevotroline&oldid=1303265292"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp