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Lisdexamfetamine



Lisdexamfetamine
Systematic (IUPAC) name
(S)-2,6-diamino-N-[(S)-1-phenylpropan-2-yl]hexanamide
Identifiers
CAS number 608137-32-2
ATC code  ?
PubChem 11597697
Chemical data
Formula C15H25N3O 
Mol. mass 263.378 g/mol
Pharmacokinetic data
Bioavailability  ?
Metabolism Hepatic
Half life < 1 hour (prodrug molecule)
Excretion Renal: ~2%
Therapeutic considerations
Pregnancy cat.

C

Legal status

Schedule II(US)

Routes Oral

Lisdexamfetamine (L-lysine-d-amphetamine) is a prodrug consisting of the psychostimulant d-amphetamine coupled with the essential amino acid L-lysine. Lisdexamfetamine was developed so that the psychostimulant is released and activated more slowly as the prodrug molecule is hydrolyzed—consequently cleaving off the amino acid-during the first pass through the intestines and/or the liver.

Additional recommended knowledge

Vyvanse is the dimesylate salt of lisdexamfetamine marketed by Shire Pharmaceuticals. Vyvanse is FDA approved—in strengths up to 70 mg—for the treatment of attention-deficit hyperactivity disorder in pediatric patients ages 6–12. Not only does Shire aspire to have Vyvanse replace Adderall XR as their flagship ADHD product, they also have their marketing target set at 50% of the ADHD pharmaceutical market share. Shire will be applying for FDA—as well as European—approval for the treatment of adolescents and adult patients with ADHD. Shire has stated prospects of applying Vyvanse for FDA approval for the treatment of depression.

A 25 mg strength Vyvanse capsule is molecularly equivalent to 10 mg Dexedrine Spansules (both the aforementioned pharmaceuticals are about 7.425 mg dextroamphetamine). 30mg is the weakest Vyvanse available (edit.) However, this molecular equivalence is not a bioequivalence ratio. While the AUC for the aforementioned pharmaceuticals is equivalent, the peak exposure of dextroamphetamine with Vyvanse is about 50% higher than that of dexedrine with Dexedrine Spansules.[1]

In human oral abuse-liability studies, 150 mg Vyvanse produced a "likeability"—euphoric effect—that was determined to be indistinguishable from 200 mg of the Schedule IV drug diethylpropion hydrochloride or 40 mg of dextroamphetamine.[2]  

Notes and references

  1. ^ FDA Approval of Vyvanse - Pharmacological Reviews
  2. ^ http://www.vyvanse.com/pdf/prescribing_information.pdf

http://www.vyvanse.com

erk wann

 
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Lisdexamfetamine". A list of authors is available in Wikipedia.
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