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SML0039

Armodafinil

≥98% (HPLC)

Synonim(y):

(R)-Modafinil; 2-[(R)-(Diphenylmethyl)sulfinyl]-acetamide, CEP 10952, CRL 40982, Nuvigil

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Informacje o tej pozycji

Wzór empiryczny (zapis Hilla):
C15H15NO2S
Numer CAS:
Masa cząsteczkowa:
273.35
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
MDL number:
Assay:
≥98% (HPLC)
Form:
powder


Quality Segment

assay

≥98% (HPLC)

form

powder

optical activity

[α]/D -15 to -20° in methanol (C=1)

color

white to tan

solubility

DMSO: ≥16 mg/mL

originator

Teva

storage temp.

2-8°C

SMILES string

NC(=O)CS(=O)C(c1ccccc1)c2ccccc2

InChI

1S/C15H15NO2S/c16-14(17)11-19(18)15(12-7-3-1-4-8-12)13-9-5-2-6-10-13/h1-10,15H,11H2,(H2,16,17)/t19-/m1/s1

InChI key

YFGHCGITMMYXAQ-LJQANCHMSA-N

Gene Information

human ... SLC6A3(6531)

Application

Armodafinil may be used in cell signaling studies.

Biochem/physiol Actions

Armodafinil has affinity for dopamine transporters and inhibits the uptake of dopamine in brain areas that are involved in the cognitive performances. It is beneficial for the patients of substance abuse and mental disorders.[1]
Armodafinil is a psychostimulant wake-promoting agent.
Armodafinil is the R isomer and longer-lasting isomer of racemic modafinil. It is a psychostimulant wake-promoting agent developed for the treatment of narcolepsy, shift work sleep disorder and excessive daytime sleepiness associated with obstructive sleep apnea
Armodafinil is a non-amphetamine, having a half-life of 10−14 hours.

Features and Benefits

This compound was developed by Teva. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.
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pictograms

Health hazardExclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Repr. 2

Klasa składowania

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



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