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Isotryptamine

From Wikipedia, the free encyclopedia
This article is about the specific substance. For the class of substances, seesubstituted isotryptamine.
Isotryptamine
Names
IUPAC name
2-indol-1-ylethanamine
Other names
2-Indolylethylamine; 2-(1-Indolyl)ethylamine; 2-(1H-Indol-1-yl)ethanamine
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/C10H12N2/c11-6-8-12-7-5-9-3-1-2-4-10(9)12/h1-5,7H,6,8,11H2
    Key: BXEFQUSYBZYTAE-UHFFFAOYSA-N
  • C1=CC=C2C(=C1)C=CN2CCN
Properties
C10H12N2
Molar mass160.220 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Isotryptamine, also known as2-(1-indolyl)ethylamine, is achemical compound andpositional isomer oftryptamine (2-(3-indolyl)ethylamine).[1] A variety of isotryptaminederivatives, orsubstituted isotryptamines, have been studied and described.[2][3][4][5][6][7]

See also

[edit]

References

[edit]
  1. ^"2-(1H-indol-1-yl)ethanamine".PubChem. Retrieved14 November 2024.
  2. ^Glennon RA, Jacyno JM, Young R, McKenney JD, Nelson D (January 1984). "Synthesis and evaluation of a novel series of N,N-dimethylisotryptamines".J Med Chem.27 (1):41–45.doi:10.1021/jm00367a008.PMID 6581313.
  3. ^Dunlap LE, Azinfar A, Ly C, Cameron LP, Viswanathan J, Tombari RJ, Myers-Turnbull D, Taylor JC, Grodzki AC, Lein PJ, Kokel D, Olson DE (February 2020)."Identification of Psychoplastogenic N,N-Dimethylaminoisotryptamine (isoDMT) Analogues through Structure-Activity Relationship Studies".J Med Chem.63 (3):1142–1155.doi:10.1021/acs.jmedchem.9b01404.PMC 7075704.PMID 31977208.
  4. ^Duan W, Cao D, Wang S, Cheng J (January 2024). "Serotonin 2A Receptor (5-HT2AR) Agonists: Psychedelics and Non-Hallucinogenic Analogues as Emerging Antidepressants".Chem Rev.124 (1):124–163.doi:10.1021/acs.chemrev.3c00375.PMID 38033123.
  5. ^Atiq MA, Baker MR, Voort JL, Vargas MV, Choi DS (May 2024)."Disentangling the acute subjective effects of classic psychedelics from their enduring therapeutic properties".Psychopharmacology (Berl).doi:10.1007/s00213-024-06599-5.PMC 12226698.PMID 38743110.
  6. ^Rasmussen K, Chytil M, Agrawal R, Leach P, Gillie D, Mungenast A, Vancutsem P, Engel S, Meyer R, Koenig A, Rus M (2024). "14. Preclinical Pharmacology of DLX-001, a Novel Non-Hallucinogenic Neuroplastogen With the Potential for Treating Neuropsychiatric Diseases".Biological Psychiatry.95 (10). Elsevier BV: S80.doi:10.1016/j.biopsych.2024.02.192.ISSN 0006-3223.
  7. ^Rasmussen K, Engel S, Chytil M, Koenig A, Meyer R, Rus M, Olson D, Salinas E (December 2023)."ACNP 62nd Annual Meeting: Poster Abstracts P251 - P500: P361. Preclinical Pharmacology of DLX-001, a Novel Non-Hallucinogenic Neuroplastogen With the Potential for Treating Neuropsychiatric Diseases".Neuropsychopharmacology.48 (Suppl 1): 211–354 (274–275).doi:10.1038/s41386-023-01756-4.PMC 10729596.PMID 38040810.
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


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