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An Entity of Type : owl:Class, within Data Space : linked.opendata.cz:8890 associated with source document(s)

AttributesValues
rdf:type
rdfs:label
  • Vorinostat
rdfs:subClassOf
Has_Target
Concept_In_Subset
Semantic_Type
  • Organic Chemical
  • Pharmacologic Substance
Preferred_Name
  • Vorinostat
NSC_Code
  • 701852
UMLS_CUI
  • C0672708
CAS_Registry
  • 149647-78-9
Accepted_Therapeutic_Use_For
  • Cutaneous T-cell Lymphoma
FDA_UNII_Code
  • 58IFB293JI
Contributing_Source
  • FDA
ALT_DEFINITION
  • A drug that is used to treat cutaneous T-cell lymphoma that does not get better, gets worse, or comes back during or after treatment with other drugs. It is also being studied in the treatment of other types of cancer. Vorinostat is a type of histone deacetylase inhibitor.NCI-GLOSS
PDQ_Open_Trial_Search_ID
  • 37944
PDQ_Closed_Trial_Search_ID
  • 37944
Chemical_Formula
  • C14H20N2O3
Legacy_Concept_Name
  • Suberoylanilide_Hydroxamic_Acid
FULL_SYN
  • N-Hydroxy-N'-phenyloctanediamideSNNCI
  • VorinostatPTNCI
  • vorinostatPTNCI-GLOSSCDR0000455153
  • SAHAPTNCI-GLOSSCDR0000455152
  • suberoylanilide hydroxamic acidSYNCI-GLOSSCDR0000044908
  • Suberanilohydroxamic AcidSYDCP09559
  • Suberanilohydroxamic AcidCNNCI
  • SAHAABNCI
  • ZolinzaPTNCI-GLOSSCDR0000514187
  • ZolinzaBRNCI
  • VORINOSTATPTFDA58IFB293JI
  • Suberoylanilide Hydroxamic AcidCNNCI
  • L-001079038CNNCI
DEFINITION
  • A synthetic hydroxamic acid derivative with antineoplastic activity. Vorinostat, a second generation polar-planar compound, binds to the catalytic domain of the histone deacetylases (HDACs). This allows the hydroxamic moiety to chelate zinc ion located in the catalytic pockets of HDAC, thereby inhibiting deacetylation and leading to an accumulation of both hyperacetylated histones and transcription factors. Hyperacetylation of histone proteins results in the upregulation of the cyclin-dependant kinase p21, followed by G1 arrest. Hyperacetylation of non-histone proteins such as tumor suppressor p53, alpha tubulin, and heat-shock protein 90 produces additional anti-proliferative effects. This agent also induces apoptosis and sensitizes tumor cells to cell death processes. Vorinostat crosses the blood-brain barrier.NCI
code
  • C1796
sameAs
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