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Agomelatine

Catalog No. A1362 Name Sigma Aldrich
CAS Number 138112-76-2 Website http://www.sigmaaldrich.com
M. F. C15H17NO2 Telephone 1-800-521-8956
M. W. 243.30098 Fax
Purity ≥98% (HPLC) Email
Storage Chembase ID: 72589

SYNONYMS

IUPAC name
N-[2-(7-methoxynaphthalen-1-yl)ethyl]acetamide
IUPAC Traditional name
agomelatine
Synonyms
S-20098
N-[2-(7-Methoxy-1-naphthalenyl)ethyl]-acetamide

DATABASE IDS

MDL Number MFCD00916659
CAS Number 138112-76-2

PROPERTIES

Empirical Formula (Hill Notation) C15H17NO2
Purity ≥98% (HPLC)
Apperance white to off-white powder
Solubility DMSO: >50 mg/mL
GHS Pictograms GHS09
GHS Signal Word Warning
GHS Hazard statements H400
European Hazard Symbols Nature polluting Nature polluting (N)
MSDS Link Download
GHS Precautionary statements P273
Risk Statements 50
Safety Statements 61
Storage Temperature 2-8°C
German water hazard class 3

DETAILS

Description (English)
Biochem/physiol Actions
Agomelatine is an extremely potent agonist at both melatonin receptors (MT1 and MT2), with additional antagonism at 5HT2C. It is a novel antidepressant with many desired in vivo properties, including neuroprotection and neurogenesis in depression-sensitive brain areas. Agomelatine′s efficacy appears to be due to both melatonergic and serotonergic properties. In neurogenesis assays, both in vitro and in vivo, the compound effects were differentially affected by antagonists for MT1/MT2 and 5HT2C, demonstrating actions through all three receptors.
Description (简体中文)
Biochem/physiol Actions
Agomelatine is an extremely potent agonist at both melatonin receptors (MT1 and MT2), with additional antagonism at 5HT2C. It is a novel antidepressant with many desired in vivo properties, including neuroprotection and neurogenesis in depression-sensitive brain areas. Agomelatine′s efficacy appears to be due to both melatonergic and serotonergic properties. In neurogenesis assays, both in vitro and in vivo, the compound effects were differentially affected by antagonists for MT1/MT2 and 5HT2C, demonstrating actions through all three receptors.

REFERENCES