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vorinostat

HDAC inhibitor · Antineoplastic agent

HDAC inhibitorAntineoplastic agent
CDSCO approved
EXCRETION
not curated
INTERACTIONS
2 major
SEVERE in our sources
PREGNANCY
D
FDA category + note
Top interactions
  • ThalidomideSevereDatabaseDDInter
  • Valproic AcidSevereDatabaseDDInter

Mechanism

Vorinostat binds to the active site of HDACs and chelates zinc ions in the active site. The resulting inhibition of HDACs causes the accumulation of acetylated histones and other acetylated proteins, among which are transcription factors crucial for cell differentiation. It inhibits the enzymatic activities of HDAC1, -2, and -3 (class I) and HDAC6 (class II).

Indications

cutaneous T-cell lymphoma with persistent or recurrent disease after two systemic therapies

Pharmacokinetics

Half-life
about 2 h (elimination)
Bioavailability
slightly improved when taken with a meal
Metabolism
glucuronidation and hydrolysis (mostly)

Side effects

Common
diarrheafatiguenauseathrombocytopeniaanorexiadysgeusia

Pregnancy & lactation

Pregnancy

D

Drug interactions

Thalidomide
Severe
Database

Clinical effect not specified

Source: DDInter

Valproic Acid
Severe
Database

Clinical effect not specified

Source: DDInter

10 additional low-confidence interactions hidden — those rows lack a documented mechanism or management plan in our sources.

Related guidelines

Other HDAC inhibitor drugs

Ask House about vorinostat

Continue into a citation-backed clinical answer with the drug context already attached.

Sources: Goodman & Gilman 14e·Verified: 2026-05-10 · House clinical team