ChemicalBook >> CAS DataBase List >>N-ACETYL-5-HYDROXYTRYPTAMINE

N-ACETYL-5-HYDROXYTRYPTAMINE

CAS No.
1210-83-9
Chemical Name:
N-ACETYL-5-HYDROXYTRYPTAMINE
Synonyms
Normelatoni;NORMELATONIN;AKOS BC-0717;N-Acetyl-5-HT;Acetylserotonin;N-ACETYLSEROTONIN;ACETYL-SEROTONINE;5-Hydroxymelatonin;O-Demethylmelatonin;MELATONINE EP IMP B
CBNumber:
CB2737409
Molecular Formula:
C12H14N2O2
Molecular Weight:
218.25
MDL Number:
MFCD00005656
MOL File:
1210-83-9.mol
Last updated:2023-06-08 09:03:03

N-ACETYL-5-HYDROXYTRYPTAMINE Properties

Melting point 120-122 °C (lit.)
Boiling point 556.8±40.0 °C(Predicted)
Density 1.268±0.06 g/cm3(Predicted)
storage temp. 2-8°C
solubility ethanol: 50 mg/mL
pka 10.09±0.40(Predicted)
form powder
color white
Stability Hygroscopic
CAS DataBase Reference 1210-83-9(CAS DataBase Reference)
FDA UNII P4TO3C82WV

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H319-H302-H335-H315
Precautionary statements  P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P-P264-P270-P301+P312-P330-P501
Safety Statements  22-24/25
WGK Germany  3
HS Code  29339900
NFPA 704
0
2 0

N-ACETYL-5-HYDROXYTRYPTAMINE price More Price(27)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich A1824 N-Acetyl-5-hydroxytryptamine ≥99% (TLC), powder 1210-83-9 100mg $153 2024-03-01 Buy
TCI Chemical A1277 N-Acetyl-5-hydroxytryptamine >98.0%(HPLC)(N) 1210-83-9 1g $453 2024-03-01 Buy
TCI Chemical A1277 N-Acetyl-5-hydroxytryptamine >98.0%(HPLC)(N) 1210-83-9 100mg $86 2024-03-01 Buy
Cayman Chemical 14535 N-Acetylserotonin ≥98% 1210-83-9 50mg $37 2024-03-01 Buy
Cayman Chemical 14535 N-Acetylserotonin ≥98% 1210-83-9 100mg $68 2024-03-01 Buy
Product number Packaging Price Buy
A1824 100mg $153 Buy
A1277 1g $453 Buy
A1277 100mg $86 Buy
14535 50mg $37 Buy
14535 100mg $68 Buy

N-ACETYL-5-HYDROXYTRYPTAMINE Chemical Properties,Uses,Production

Chemical Properties

white to off-white or slightly pink powder

Uses

A metabolite of Melatonin (M215000).

Uses

N-Acetyl-5-hydroxytryptamine has been used to treat neuron cells and to analyze its effects on?Krüppel-like factor 15 (KLF15) expression.

Definition

ChEBI: A member of the class of hydroxyindoles that is the N-acetyl derivative of serotonin.

General Description

N-Acetylserotonin (NAS)/normelatonin acts as a precursor of melatonin in the tryptophan metabolic pathway.

Biological Activity

n-acetylserotonin is an agonist at the melatonin receptors mt1, mt2, and mt3.a melatonin receptor is a g protein-coupled receptor binding melatonin. three types of melatonin receptor have been identified. the mt1 and mt2 receptor subtypes are in humans and other mammals, whereas an additional melatonin receptor subtype mt3 has been identified in amphibia and birds.

Biochem/physiol Actions

N-acetyl-serotonin (NAS/normelatonin) can act as a shelter to neurons due to its protecting ability against oxidative challenges. It can also repress the actions of the transcription factor NF-kappaB. NAS possesses antioxidant and antiaging actions. It has protective action against β-amyloid induced neurotoxicity. It helps to maintain the optimal fluidity of the biological membranes.

in vitro

n-acetylserotonin, a precursor of melatonin, was acetylated from serotonin by arylalkylamine nacetyltransferase (aanat). n-acetylserotonin was found to be able to swiftly activate trkb in a circadian manner. n-acetylserotonin also exhibited antidepressant effect in a trkb-dependent manner. in additioin, n-acetylserotonin could rapidly activate trkb, but not trka or trkc, in a neurotrophin- and mt3 receptor-independent manner. moreover, n-acetylserotonin, but not melatonin, showed a robust antidepressant-like behavioral effect in a trkb-dependent way [1].

in vivo

animal study found that in bdnf knockout mice the administration of n-acetylserotonin could activate trkb. moreover, the endogenous trkb was activated in wild-type c3h/f+/+ mice but not in aanat-mutated c57bl/6j mice, in a circadian rhythm. in addition, trkb activation was found to be high at night in the dark and low during the day [1].

References

[1] jang, s. w.,liu, x.,pradoldej, s., et al. n-acetylserotonin activates trkb receptor in a circadian rhythm. proceedings of the national academy of sciences of the united states of america 107(8), 3876-3881 (2010).

N-ACETYL-5-HYDROXYTRYPTAMINE Preparation Products And Raw materials

Global( 172)Suppliers
Supplier Tel Email Country ProdList Advantage
Capot Chemical Co.,Ltd.
571-85586718 +8613336195806 sales@capotchem.com China 29797 60
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29914 58
Chongqing Chemdad Co., Ltd
+86-023-61398051 +8613650506873 sales@chemdad.com China 39916 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
Hefei TNJ Chemical Industry Co.,Ltd.
0551-65418671 sales@tnjchem.com China 34572 58
HANGZHOU CLAP TECHNOLOGY CO.,LTD
86-571-88216897,88216896 13588875226 sales@hzclap.com CHINA 6313 58
Unipharm pharmaceutical industry Co., Ltd
536-8266195 +8613953676784 lee@unipharm-sd.com China 1206 58
Dayang Chem (Hangzhou) Co.,Ltd.
571-88938639 +8617705817739 info@dycnchem.com CHINA 52867 58
PT CHEM GROUP LIMITED
+86-85511178 +86-85511178 peter68@ptchemgroup.com China 35453 58
GIHI CHEMICALS CO.,LIMITED
+8618058761490 info@gihichemicals.com China 50000 58

View Lastest Price from N-ACETYL-5-HYDROXYTRYPTAMINE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
N-ACETYL-5-HYDROXYTRYPTAMINE pictures 2019-07-06 N-ACETYL-5-HYDROXYTRYPTAMINE
1210-83-9
US $100.00 / KG 1KG 99% Cusstomized Career Henan Chemical Co
N-Acetyl-5-hydroxytryptamine, 3-(N-Acetyl-2-aminoethyl)-5-hydroxyindole, 98% N-Acetyl-5-hydroxytryptamine,N-Acetylserotonin, Normelatonin 3-(2-Acetamidoethyl)-5-hydroxyindole N-Acetylserotonin N-Acetylserotonin, Normelatonin Acetylserotonin N-Acetyl-5-HT N-Acetyl-5-hydroxy-1H-indole-3-ethaneamine N-Acetyl-5-hydroxytryptamine,99% AcetaMide,N-[2-(5-hydroxy-1H-indol-3-yl)ethyl]- O-Demethylmelatonin N-Acetyl-5-hydroxytryptamine 3-(2-ACETAMIDOETHYL)-5-HYDROXYINDOLE SEROTONIN, N-ACETYL- NORMELATONIN N-[2-(5-HYDROXY-1H-INDOL-3-YL)ETHYL]ACETAMIDE N-ACETYLSEROTONIN N-ACETYL-5-HYDROXYTRYPTAMINE N-ALPHA-ACETYL SEROTONINE ACETYL-SEROTONINE ACETYL-SEROTONIN, N- ACETYL-5-HYDROXY TRYPTAMINE AKOS BC-0717 3-(N-ACETYL-2-AMINOETHYL)-5-HYDROXYINDOLE 5-Hydroxymelatonin 5-Hydroxy-N-acetyltryptamine Normelatoni N-[2-(5-hydroxy-1H-indol-3-yl)ethyl]ethanamide N-Acetyl-5-hydroxytrytamine N-Acetyl-5-hydroxytryptamine;N-Acetylserotonin N-Acetyl-5-hydroxytryptamine > Serotonin Impurity 5 Melatonin Impurtiy 2 Melatonin EP Impurity B MELATONINE EP IMP B 1210-83-9 Immediate precursor of melatonin. It is formed from serotonin and acetyl-CoA in a reaction catalyzed by serotonin N-acetyl transferase, the rate-limiting enzyme in melatonin biosynthesis. Heterocyclic Building Blocks Tryptamines Indoles Building Blocks Various Metabolites and Impurities Indoles Intermediates & Fine Chemicals Metabolites & Impurities Pharmaceuticals Heterocyclic Compounds Tryptamines Amino Acids Metabolites & Impurities, Pharmaceuticals, Intermediates & Fine Chemicals