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Details

Stereochemistry ACHIRAL
Molecular Formula C10H12N2O2
Molecular Weight 192.2145
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 5,6-DIHYDROXYTRYPTAMINE

SMILES

NCCC1=CNC2=CC(O)=C(O)C=C12

InChI

InChIKey=SKOKLDQYOKPCPU-UHFFFAOYSA-N
InChI=1S/C10H12N2O2/c11-2-1-6-5-12-8-4-10(14)9(13)3-7(6)8/h3-5,12-14H,1-2,11H2

HIDE SMILES / InChI

Molecular Formula C10H12N2O2
Molecular Weight 192.2145
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Serotonin receptors are involved in the spinal mediation of descending facilitation of surgical incision-induced increase of Fos-like immunoreactivity in rats.
2010-03-23
Regeneration of 5-HT fibers in hippocampal heterotopia of methylazoxymethanol-induced micrencephalic rats after neonatal 5,7-DHT injection.
2010-03
Histone H3 Acetylation is Asymmetrically Induced Upon Learning in Identified Neurons of the Food Aversion Network in the Mollusk Helix Lucorum.
2010
Response disengagement on a spatial self-ordered sequencing task: effects of regionally selective excitotoxic lesions and serotonin depletion within the prefrontal cortex.
2009-05-06
Interactions between dopamine and melatonin organize circadian rhythmicity in the retina of the green iguana.
2007-12
Amphetamine and mCPP effects on dopamine and serotonin striatal in vivo microdialysates in an animal model of hyperactivity.
2007-02
Comparative studies of the effects of chlorpromazine and 5,6-dihydroxytryptamine on locomotion, defensive reactions in the snail Helix lucorum, and command neuron excitability in long-term sensitization.
2006-09
Involvement of supraspinal imidazoline receptors and descending monoaminergic pathways in tizanidine-induced inhibition of rat spinal reflexes.
2005-09
[Comparative investigation of influence of injections of chlorpromazine and 5,6-dihydroxytryptamine on locomotion, defensive reactions of snall helix lucorum and excitability of command neurons in long-term sensitization].
2005-07
Imidazoline receptors associated with noradrenergic terminals in the rostral ventrolateral medulla mediate the hypotensive responses of moxonidine but not clonidine.
2005
Opposite morphological responses of partially denervated cortical serotonergic and noradrenergic axons to repeated stress in adult rats.
2004-07-30
The 5-HT3 receptor facilitates at-level mechanical allodynia following spinal cord injury.
2004-07
Interaction between serotonergic and noradrenergic axons during axonal regeneration.
2003-11
Global 5-HT depletion attenuates the ability of amphetamine to decrease impulsive choice on a delay-discounting task in rats.
2003-11
Elimination of serotonergic cells induces a marked increase in generation of dopaminergic neurons from mesencephalic precursors.
2003-10
Electrophysiological studies of the effects of 5,6-dihydroxytryptamine on the acquisition of a conditioned defensive reflex in snails.
2003-07
Comparative effects of injecting 5,6-dihydroxytryptamine in the dorsal or medial raphe nuclei on rat puberty.
2003-05-15
7-Hydroxytryptophan, a novel, specific, cytotoxic agent for carcinoids and other serotonin-producing tumors.
2002-06-15
Monoamine neurotoxins-induced apoptosis in lymphocytes by a common oxidative stress mechanism: involvement of hydrogen peroxide (H(2)O(2)), caspase-3, and nuclear factor kappa-B (NF-kappaB), p53, c-Jun transcription factors.
2002-02-15
[Electrophysiological study of 5,6-dihydroxytryptamine effect on defensive reflex conditioning in the snail].
2002-02
Serotonin modulates expression of VIP and GRP mRNA via the 5-HT(1B) receptor in the suprachiasmatic nucleus of the rat.
2001-10
Studies on the behavioral and hypotensive effects of intraventricular prostacyclin (PGI2) in rats.
1981-11
Turning in MFB-lesioned rats and antagonism of neuroleptic-induced catalepsy after lisuride and LSD.
1978-05-08
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:20:42 GMT 2025
Edited
by admin
on Mon Mar 31 19:20:42 GMT 2025
Record UNII
W2QY253O8S
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1H-INDOLE-5,6-DIOL, 3-(2-AMINOETHYL)-
Preferred Name English
5,6-DIHYDROXYTRYPTAMINE
Systematic Name English
3-(2-AMINOETHYL)INDOLE-5,6-DIOL
Systematic Name English
INDOLE-5,6-DIOL, 3-(2-AMINOETHYL)-
Systematic Name English
Code System Code Type Description
PUBCHEM
21163
Created by admin on Mon Mar 31 19:20:42 GMT 2025 , Edited by admin on Mon Mar 31 19:20:42 GMT 2025
PRIMARY
EPA CompTox
DTXSID40198930
Created by admin on Mon Mar 31 19:20:42 GMT 2025 , Edited by admin on Mon Mar 31 19:20:42 GMT 2025
PRIMARY
ECHA (EC/EINECS)
225-810-3
Created by admin on Mon Mar 31 19:20:42 GMT 2025 , Edited by admin on Mon Mar 31 19:20:42 GMT 2025
PRIMARY
CAS
5090-36-8
Created by admin on Mon Mar 31 19:20:42 GMT 2025 , Edited by admin on Mon Mar 31 19:20:42 GMT 2025
PRIMARY
FDA UNII
W2QY253O8S
Created by admin on Mon Mar 31 19:20:42 GMT 2025 , Edited by admin on Mon Mar 31 19:20:42 GMT 2025
PRIMARY