ChemicalBook > CAS DataBase List > AgoMelatine-D6

AgoMelatine-D6

Product Name
AgoMelatine-D6
CAS No.
1079389-42-6
Chemical Name
AgoMelatine-D6
Synonyms
S-20098 D6;AgoMelatine-D6;[2H6]-Agomelatine;Beflubutamid Impurity 4 (Bromobutide);Acetamide-2,2,2-d3, N-[2-[7-(methoxy-d3)-1-naphthalenyl]ethyl]-;Agomelatine D6Q: What is Agomelatine D6 Q: What is the CAS Number of Agomelatine D6 Q: What is the storage condition of Agomelatine D6 Q: What are the applications of Agomelatine D6
CBNumber
CB12646212
Molecular Formula
C15H11D6NO2
Formula Weight
249.34
MOL File
1079389-42-6.mol
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AgoMelatine-D6 Property

storage temp. 
Store at -20°C
solubility 
Methanol: soluble
form 
A solid
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
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N-Bromosuccinimide Price

Cayman Chemical
Product number
26447
Product name
Agomelatine-d6
Packaging
1mg
Price
$359
Updated
2024/03/01
TRC
Product number
A430003
Product name
Agomelatine-d6
Packaging
10mg
Price
$1320
Updated
2021/12/16
ChemScene
Product number
CS-0019795
Product name
AgomelatineD6
Packaging
1mg
Price
$280
Updated
2021/12/16
Medical Isotopes, Inc.
Product number
D32833
Product name
Agomelatine-d6
Packaging
1mg
Price
$490
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
RDL0014212
Product name
AGOMELATINE-D6
Purity
95.00%
Packaging
5MG
Price
$497.17
Updated
2021/12/16
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AgoMelatine-D6 Chemical Properties,Usage,Production

Uses

Agomelatine-d6 is labelled Agomelatine (A430000) which is a melatoninergic agonist and selective antagonist of 5-HT2C receptors, and has been shown to be active in several animal models of depression. Agomelatine (S20098) displayed pKi values of 6.4 and 6.2 at native (porcine) and cloned, human (h)5-hydroxytryptamine (5-HT)2C receptors, respectively.

Biological Activity

Agomelatine-d6 is intended for use as an internal standard for the quantification of agomelatine by GC- or LC-MS. Agomelatine is an agonist of melatonin (MT) receptors and a derivative of melatonin .1 It binds to MT1 and MT2 receptors (Kis = 0.14 and 0.41 nM, respectively) and has an EC50 value of 0.1 nM in a [35S]GTPγS binding assay using CHO cells expressing MT2 receptors. Agomelatine is also an antagonist of the serotonin (5-HT) receptor subtypes 5-HT2B and 5-HT2C (Kis = 0.26 and 0.71 nM, respectively, for the human receptors).2 Agomelatine (40 mg/kg) inhibits the penile erection response induced by the 5-HT2 agonist Ro 60-0175 in rats. It also increases extracellular levels of noradrenaline and dopamine in the frontal cortex of freely moving rats when administered at doses ranging from 20 to 80 mg/kg. Agomelatine (10 mg/kg) reduces immobility time in the forced swim test and increases the amount of time spent in the open arms of the elevated plus maze, indicating antidepressant-like and anxiolytic-like activity, in a transgenic neuroendocrine model of depression.3 It also increases the rate of readjustment to circadian activity cycles following an induced phase shift.

References

1.Poissonnier-Durieux, S., Ettaoussi, M., Pérès, B., et al.Synthesis of 3-phenylnaphthalenic derivatives as new selective MT2 melatoninergic ligandsBioorg. Med. Chem.16(18)8339-8348(2008) 2.Millan, M.J., Gobert, A., Lejeune, F., et al.The novel melatonin agonist agomelatine (S20098) is an antagonist at 5-hydroxytryptamine2C receptors, blockade of which enhances the activity of frontocortical dopaminergic and adrenergic pathwaysJ. Pharmacol. Exp. Ther.306(3)954-964(2003) 3.Barden, N., Shink, E., Labbé, M., et al.Antidepressant action of agomelatine (S 20098) in a transgenic mouse modelProg. Neuropsychopharmacol. Biol. Psychiatry29(6)908-916(2005)

AgoMelatine-D6 Preparation Products And Raw materials

Raw materials

Preparation Products

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