Vorinostat

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Vorinostat
Systematic (IUPAC) name
N-hydroxy-N'-phenyl-octanediamide
Identifiers
CAS number 149647-78-9
ATC code  ?
PubChem 5311
Chemical data
Formula C14H20N2O3 
Mol. mass 264.32 g/mol
Pharmacokinetic data
Bioavailability  ?
Protein binding 71%
Metabolism Hepatic glucuronidation and oxidation
CYP system not involved
Half life 2 hours
Excretion Renal (negligible)
Therapeutic considerations
Licence data

US

Pregnancy cat.

D(US)

Legal status

-only(US)

Routes Oral

Vorinostat (rINN) or suberoylanilide hydroxamic acid (SAHA) is a member of a larger class of compounds that inhibit histone deacetylases (HDAC). Histone deacetylase inhibitors (HDI) have a broad spectrum of epigenetic activities. SAHA is marketed under the name Vorinostat, brand name Zolinza, for the treatment of cutaneous T cell lymphoma (CTCL), a type of skin cancer, to be used when the disease persists, gets worse, or comes back during or after treatment with other medicines. It has been used to treat Sézary's disease.[1]

A recent study suggested that vorinostat also possesses some activity against recurrent glioblastoma multiforme, resulting in a median overall survival of 5.7 months (compared to 4 - 4.4 months in earlier studies). Further brain tumor trials are planned in which vorinostat will be combined with other drugs.

Zolinza was approved by the U.S. Food and Drug Administration (FDA) for the treatment of CTCL on October 6, 2006, and it is manufactured by Patheon, Inc., in Mississauga, Ontario, Canada, for Merck & Co., Inc., White House Station, New Jersey.

[edit] References

  1. ^ Cuneo A, Castoldi. Mycosis fungoidses/Sezary's syndrome. Retrieved on 2008-02-15.
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