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Serotonin HCl

Catalog No.
B1830
Endogenous 5-HT receptor agonist
Grouped product items
SizePriceStock Qty
10mM (in 1mL DMSO)
$60.00
In stock
50mg
$50.00
In stock
For scientific research use only and should not be used for diagnostic or medical purposes.

Tel: +1-832-696-8203

Email: [email protected]

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Background

Serotonin hydrochloride is a monoamine neurotransmitter in the central nervous system and an endogenous 5-HT receptor agonist. Serotonin hydrochloride is also a catechol O-methyltransferase (COMT) inhibitor with a Ki of 44 μM.

It is biochemically derived from tryptophan, and it plays an important role in the regulation of mood, sleep, vomiting, sexuality, and appetite. Several disorders are linked to low levels of serotonin, including depression, migraines, bipolar disorder, and anxiety. Its actions are wiped off primarily by uptake of serotonin from the synapse. Serotonin reuptake can be inhibited with cocaine, MDMA, tricyclic antidepressants, and selective serotonin reuptake inhibitors.

In vitro: Serotonin hydrochloride is a monoamine neurotransmitter in the central nervous system and an endogenous 5-HT receptor agonist. Serotonin hydrochloride can also inhibit catechol O-methyltransferase (COMT), an enzyme causing to modulation the perception of pain, via non-competitive binding to the site bound by catechol substrates with a binding affinity comparable to the binding affinity of catechol itself (Ki= 44 μM). Results demonstrate that addition of 100 μM of Serotonin hydrochloride reduces the reaction velocity of COMT.

In vivo: Serotonin hydrochloride produces robust hypersensitivity comparing to saline-treated controls (p<0.001). Compared to IL-13 receiving vehicle following induction of DSS colitis. Obvious growth in colonic 5-HT content is observed in IL-13 mice receiving Serotonin hydrochloride. 

References:

1. Tsao D, et al. Serotonin-induced hypersensitivity via inhibition of catechol O-methyltransferase activity. Mol Pain. 2012 Apr 13;8:25.

2. Shajib MS, et al. Interleukin 13 and serotonin: linking the immune and endocrine systems in murine models of intestinal inflammation. PLoS One. 2013 Aug 28;8(8):e72774.

3. Martínez A, Knappskog PM, Haavik J. A structural approach into human tryptophan hydroxylase and its implications for the regulation of serotonin biosynthesis. Curr Med Chem. 2001 Jul;8(9):1077-91. Review. PubMed PMID: 11472242.

4. Liu Q, Yang Q, Sun W, Vogel P, Heydorn W, Yu XQ, Hu Z, Yu W, Jonas B, Pineda R, Calderon-Gay V, Germann M, O'Neill E, Brommage R, Cullinan E, Platt K, Wilson A, Powell D, Sands A, Zambrowicz B, Shi ZC. Discovery and characterization of novel tryptophan hydroxylase inhibitors that selectively inhibit serotonin synthesis in the gastrointestinal tract. J Pharmacol Exp Ther. 2008 Apr;325(1):47-55. doi: 10.1124/jpet.107.132670. Epub 2008 Jan 11. PubMed PMID: 18192499.

Chemical Properties

Physical AppearanceA solid
StorageStore at -20°C
M.Wt212.68
Cas No.153-98-0
FormulaC10H12N2O·HCl
Solubility≥11.12 mg/mL in EtOH with ultrasonic; ≥22.35 mg/mL in H2O; ≥8.2 mg/mL in DMSO
Chemical Name3-(2-aminoethyl)-1H-indol-5-ol;hydrochloride
SDFDownload SDF
Canonical SMILESC1=CC2=C(C=C1O)C(=CN2)CCN.Cl
Shipping ConditionSmall Molecules with Blue Ice, Modified Nucleotides with Dry Ice.
General tips We do not recommend long-term storage for the solution, please use it up soon.

Quality Control

Chemical structure

Serotonin HCl