H9523

Serotonin hydrochloride

≥98%, powder, neurotransmitter

• Synonyme(s) : 3-(2-Aminoethyl)-5-hydroxyindole hydrochloride, 5-HT, 5-Hydroxytryptamine hydrochloride
• Formule empirique (notation de Hill): C₁₀H₁₂N₂O · HCl
• Numéro CAS: 153-98-0
• Poids moléculaire : 212.68
• Numéro Beilstein : 3570963
• Numéro MDL: MFCD00012686
• Code UNSPSC : 12352200
• ID de substance PubChem : 24278124
• Nomenclature NACRES : NA.77

Propriétés

• product name: Serotonin hydrochloride, powder
• Pureté: ≥98%
• Niveau de qualité: 200
• Forme: powder
• Couleur: white to off-white
• Pf: 149-154 °C (lit.)
• Solubilité: H₂O: 17 mg/mL; 0.1 M HCl: 22 mg/mL; ethanol: 5.3 mg/mL
• Température de stockage: 2-8°C
• Chaîne SMILES: Cl[H].NCCc1c[nH]c2ccc(O)cc12
• InChI: 1S/C10H12N2O.ClH/c11-4-3-7-6-12-10-2-1-8(13)5-9(7)10;/h1-2,5-6,12-13H,3-4,11H2;1H
• Clé InChI: MDIGAZPGKJFIAH-UHFFFAOYSA-N
• Informations sur le gène: human ... HTR3A(3359)

Description

Description générale

Serotonin is a ubiquitous molecule found in all animals. It shows diverse effects in the central and peripheral nervous system (CAN/PNS). Serotonin acts as a hormone and as a mitogen. It is produced in the axon terminal present in the brain. Action potential induces the release of serotonin that diffuses across the synapse to turn on the post-synaptic receptors. Serotonin plays a crucialrole in development, respiration, thermoregulation, endocrine, cardiovascular, and gastrointestinal functions. It also plays a role in sensory perceptional behaviors such as the sleep-wake cycle, sex, mood, memory, aggression, pain sensitivity, learning, and cognition. Serotonin impacts several psychiatric disorders such as schizophrenia, anorexia nervosa, depression, and a range of anxiety disorders such as obsessive-compulsive disorder, panic attacks, and social phobia. Variations in serotonin levels are associated withimpulse-related disorders or personalities like substance abuse, gambling, attention deficit disorder, obsessive-control, and aggression.

Application

Serotonin hydrochloride hasbeen used: to study the mechanisms of 5-hydroxytryptamine receptor antagonistsregulate fibrosis in liver spheroids, to study its effects on theextracellular-related-kinase (ERK) phosphorylation in human embryonic kidneycells, in transwell assay, wound healing assay and tumor allograft assay incolon carcinoma cell line

Actions biochimiques/physiologiques

Neurotransmitter.

Caractéristiques et avantages

This compound is featured on the Biogenic Amine Transporters page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

Notes préparatoires

Solutions should be freshly prepared.

Informations sur la sécurité

• Pictogrammes: GHS06,GHS08
• Mention d'avertissement: Danger
• Mentions de danger: H301,H361
• Conseils de prudence: P202 - P264 - P280 - P301 + P310 - P405 - P501
• Classification des risques: Acute Tox. 3 Oral - Repr. 2
• Code de la classe de stockage: 6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
• Classe de danger pour l'eau (WGK): WGK 3
• Point d'éclair (°F): Not applicable
• Point d'éclair (°C): Not applicable
• Équipement de protection individuelle: dust mask type N95 (US), Eyeshields, Gloves