Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

Indorenate

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Indorenate
Identifiers
  • methyl 3-amino-2-(5-methoxy-1H-indol-3-yl)propanoate
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC13H16N2O3
Molar mass248.282 g·mol−1
3D model (JSmol)
  • COC(=O)C(CN)c1c[nH]c(ccc2OC)c1c2
  • InChI=1S/C13H16N2O3/c1-17-8-3-4-12-9(5-8)11(7-15-12)10(6-14)13(16)18-2/h3-5,7,10,15H,6,14H2,1-2H3 ☒N
  • Key:YFEDJMLMWJSRJJ-UHFFFAOYSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Indorenate (TR-3369), is atryptaminederivative which acts as anagonist at the5-HT1A,5-HT1B and5-HT2Cserotoninreceptors. It hasanxiolytic,antihypertensive andanorectic effects, predominantly through action at 5-HT1A, but with some contribution from the 5-HT1B and 5-HT2C subtypes, and possibly some other non-serotonergic targets also.[1][2][3][4][5][6][7][8][9]

See also

[edit]

References

[edit]
  1. ^Antonaccio MJ, Kerwin L (1981)."On the effects and mechanism of action of the antihypertensive agent TR 3369 (5-methoxytryptamine beta-methylcarboxylate) in spontaneously hypertensive rats".Journal of Cardiovascular Pharmacology.3 (6):1306–11.doi:10.1097/00005344-198111000-00018.PMID 6173531.S2CID 53762649.
  2. ^Schoeffter P, Hoyer D (November 1988)."Centrally acting hypotensive agents with affinity for 5-HT1A binding sites inhibit forskolin-stimulated adenylate cyclase activity in calf hippocampus".British Journal of Pharmacology.95 (3):975–85.doi:10.1111/j.1476-5381.1988.tb11728.x.PMC 1854240.PMID 3207999.
  3. ^Fernández-Guasti A, Escalante A, Hong E, Agmo A (September 1990). "Behavioural actions of the serotonergic anxiolytic indorenate".Pharmacology Biochemistry and Behavior.37 (1):83–8.doi:10.1016/0091-3057(90)90045-J.PMID 1979877.S2CID 22146281.
  4. ^López Cabrera M, Velázquez Martínez DN, Prado R, García G, Ortiz R (1991). "Effects of the intracerebroventricular administration of indorenate and fenfluramine on spontaneous behavior and food intake in rats".Proceedings of the Western Pharmacology Society.34:465–8.PMID 1788330.
  5. ^Velázquez-Martínez DN, López Cabrera M, Sánchez H, Ramírez JI, Hong E (March 1999)."Discriminative stimulus properties of indorenate, a serotonin agonist".Journal of Psychiatry & Neuroscience.24 (2):122–30.PMC 1188992.PMID 10212554.
  6. ^Sánchez H, Velázquez-Martínez DN (March 2001). "Discriminative stimulus properties of indorenate, a 5-HT1A, 5-HT1B and 5-HT2C agonist: a study in rats".Journal of Psychopharmacology.15 (1):29–36.doi:10.1177/026988110101500106.PMID 11277605.S2CID 13257797.
  7. ^Miranda F, Orozco G, Velázquez-Martínez DN (July 2002). "Full substitution of the discriminative cue of a 5-HT(1A/1B/2C) agonist with the combined administration of a 5-HT(1B/2C) and a 5-HT(1A) agonist".Behavioural Pharmacology.13 (4):303–11.doi:10.1097/00008877-200207000-00007.PMID 12218511.S2CID 24468773.
  8. ^Miranda F, Hong E, Sánchez H, Velázquez-Martínez DN (January 2003). "Further evidence that the discriminative stimulus properties of indorenate are mediated by 5-HT 1A/1B/2C receptors".Pharmacology Biochemistry and Behavior.74 (2):371–80.doi:10.1016/S0091-3057(02)01010-9.PMID 12479957.S2CID 23429292.
  9. ^López-Meraz ML, Neri-Bazán L, Rocha L (September 2006)."Indorenate modifies a1-adrenergic and benzodiazepine receptor binding in the rat brain: an autoradiography study".The Journal of Pharmacy and Pharmacology.58 (9):1243–8.doi:10.1211/jpp.58.9.0011.PMID 16945183.S2CID 44723130.
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
Tryptamines
4-Hydroxytryptamines
andesters/ethers
5-Hydroxy- and
5-methoxytryptamines
N-Acetyltryptamines
α-Alkyltryptamines
Cyclized tryptamines
Isotryptamines
Related compounds


Stub icon

This article about ananxiolytic is astub. You can help Wikipedia byexpanding it.

Retrieved from "https://en.wikipedia.org/w/index.php?title=Indorenate&oldid=1282635512"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp