Article · Wikipedia archive · Last revised Jun 3, 2026

7-Hydroxytryptamine

7-Hydroxytryptamine (7-HT) is a serotonin receptor modulator of the tryptamine family. It is the 7-hydroxy derivative of tryptamine and is a positional isomer of serotonin.

Last revised
Jun 3, 2026
Read time
≈ 2 min
Length
462 w
Citations
16
Source
7-Hydroxytryptamine
Clinical data
Other names7-HT; 7-OH-T; 7-HO-T; 7-Hydroxy-T
Drug classSerotonin receptor modulator; Monoamine reuptake inhibitor; Monoamine releasing agent
ATC code
  • None
Identifiers
  • 3-(2-aminoethyl)-1H-indol-7-ol
CAS Number
PubChem CID
ChemSpider
Chemical and physical data
FormulaC10H12N2O
Molar mass176.219 g·mol−1
3D model (JSmol)
  • C1=CC2=C(C(=C1)O)NC=C2CCN
  • InChI=1S/C10H12N2O/c11-5-4-7-6-12-10-8(7)2-1-3-9(10)13/h1-3,6,12-13H,4-5,11H2
  • Key:RETCYVKOCFWWTL-UHFFFAOYSA-N

7-Hydroxytryptamine (7-HT) is a serotonin receptor modulator of the tryptamine family.123 It is the 7-hydroxy derivative of tryptamine and is a positional isomer of serotonin (5-hydroxytryptamine; 5-HT).12

The drug shows sympathomimetic effects similarly to serotonin.14 On the other hand, similarly to 6-hydroxytryptamine but in contrast to serotonin, it showed little or no activity as a serotonin receptor agonist in the rabbit thoracic aorta, which expresses serotonin 5-HT2 receptors.2 The drug is known to act as a serotonin–norepinephrine–dopamine reuptake inhibitor (SNDRI), with greater potency on catecholamine reuptake than serotonin reuptake, whereas its possible effects in terms of monoamine release induction were not assessed.5 However, in other studies, 7-HT was reported to increase serotonin and norepinephrine release.6748 It did not show the long-lasting monoaminergic neurotoxicity of certain related compounds like 5,7-dihydroxytryptamine (5,7-DHT) in rodents.59

7-HT was first described in the scientific literature by Irvine Page by 1952.1

See also

See also

References

References

  1. Page IH (May 1952). "The vascular action of natural serotonin, 5- and 7-hydroxytryptamine and tryptamine". The Journal of Pharmacology and Experimental Therapeutics. 105 (1): 58–73. doi:10.1016/S0022-3565(25)05007-4. PMID 14939154.
  2. Clancy BM, Maayani S (June 1985). "5-Hydroxytryptamine receptor in isolated rabbit aorta: characterization with tryptamine analogs". The Journal of Pharmacology and Experimental Therapeutics. 233 (3): 761–769. doi:10.1016/S0022-3565(25)22895-6. PMID 4009488.
  3. Branchek T, Kates M, Gershon MD (December 1984). "Enteric receptors for 5-hydroxytryptamine". Brain Research. 324 (1): 107–118. doi:10.1016/0006-8993(84)90627-9. PMID 6518379.
  4. Göthert M, Dührsen U (July 1979). "Effects of 5-hydroxytryptamine and related compounds on the sympathetic nerves of the rabbit heart". Naunyn-Schmiedeberg's Archives of Pharmacology. 308 (1): 9–18. doi:10.1007/BF00499713. PMID 492358.
  5. Horn AS, Baumgarten HG, Schlosserberger HG (July 1973). "Inhibition of the uptake of 5-hydroxytryptamine, noradrenaline and dopamine into rat brain homogenates by various hydroxylated tryptamines". Journal of Neurochemistry. 21 (1): 233–236. doi:10.1111/j.1471-4159.1973.tb04242.x. PMID 4720899.
  6. Göthert M, Schlicker E (March 1983). "Autoreceptor-mediated inhibition of 3H-5-hydroxytryptamine release from rat brain cortex slices by analogues of 5-hydroxytryptamine". Life Sciences. 32 (11): 1183–1191. doi:10.1016/0024-3205(83)90186-8. PMID 6572776.
  7. Paton DM (November 1973). "Letter: Effect of substituted tryptamines on the efflux of noradrenaline from adrenergic nerves in rabbit atria". The Journal of Pharmacy and Pharmacology. 25 (11): 905–907. doi:10.1111/j.2042-7158.1973.tb09971.x. PMID 4149655.
  8. Daly JW, Creveling CR, Witkop B (May 1966). "The chemorelease of norepinephrine from mouse hearts. Structure-activity relationships. I. Sympathomimetic and related amines". Journal of Medicinal Chemistry. 9 (3): 273–280. doi:10.1021/jm00321a001. PMID 5960887.
  9. Lachenmayer L, Groth HP (July 1973). "Degeneration and regeneration of the adrenergic nerves in the rat iris induced by dihydroxytryptamines". Virchows Archiv. B, Cell Pathology. 13 (3) 197: 197–213. doi:10.1007/BF02889308. PMID 4201204.