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Names

6-HO-T
6-Hydroxytryptamine

IUPAC name

3-(2-Aminoethyl)-1H-indol-6-ol

ID 5738 · Formula C₁₀H₁₂N₂O · Molecular weight 176.215

Tags Tryptamine

InChI InChI=1S/C10H12N2O/c11-4-3-7-6-12-10-5-8(13)1-2-9(7)10/h1-2,5-6,12-13H,3-4,11H2

InChI Key WZTKTNRVJAMKAS-UHFFFAOYSA-N This stereoisomer Any stereoisomer

SMILES NCCc1c[nH]c2c1ccc(c2)O

ChemSpider 141007
PubChem 160463
Wikidata Q83069196

Kalir, A; Szara, S. Synthesis and pharmacological activity of alkylated tryptamines. J. Med. Chem., 1 May 1966, 9 (3), 341–344. 482 kB. https://doi.org/10.1021/jm00321a017 #22

Wiseman-Distler, MH; Sourkes, TL. The effect of 4-hydroxyindoles on the metabolism of 5-hydroxytryptamine (serotonin). Ann. N. Y. Acad. Sci., 1 Jan 1962, 96 (1), 142–151. 458 kB. https://doi.org/10.1111/j.1749-6632.1962.tb50109.x

Hoffer, A; Osmond, H. The Hallucinogens, Academic Press, New York, . 3.9 MB. #6-Hydroxytryptamine

Brimblecombe, RW; Pinder, RM. Hallucinogenic agents, Wright-Scientechnica, Bristol, UK, 1 Jan 1975. 46.2 MB. #Page 106

Gupta, SP; Singh, P; Bindal, MC. QSAR studies on hallucinogens. Chem. Rev., 1 Dec 1983, 83 (6), 633–649. 2.8 MB. https://doi.org/10.1021/cr00058a003 #105

4-HO-T · 4-Hydroxytryptamine

5-HO-T · 5-HT · 5-Hydroxytryptamine · Serotonin

4-MAR · 4-MAX · 4-Methylaminorex

4′-Methylaminorex

1494

3′-Methylaminorex

10198

10202

12015

3-MAR · 3-Methylaminorex

7-HO-T · 7-Hydroxytryptamine

7993

7987

Cotinine

7 Dec 2019 · · Isomer Design