Vorinostat
Vorinostat
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.
Also known as L-001079038, MSK-390, N-Hydroxy-N'-phenyloctanediamide, SAHA, Suberanilohydroxamic Acid, Suberoylanilide Hydroxamic Acid, VORINOSTAT, Zolinza — per NCIT
Also identified as
- ATC L01XH01 per RXNORM
- NCIT NCIT:C1796 per NCIT
- SCTID 422505001 per RXNORM
- SCTID 422523009 per RXNORM
- UNII 58IFB293JI per RXNORM
Indications
| Disease | Relation | Source |
|---|---|---|
| Primary cutaneous T-cell non-Hodgkin lymphoma | may treat | MEDRT · Public domain (U.S. Government work) |
Organ Effects
| Organ | Side effect / interaction | Source |
|---|---|---|
| Lymphoid system | may treat a disease of this organ | DERIVED · CC BY 4.0 |
| Skin of body | may treat a disease of this organ | DERIVED · CC BY 4.0 |
2 entries above are marked DERIVED: Atlas Médico inferred them by combining two sourced claims, and no source asserts these links directly. Treat them as a navigation aid, not as a clinical statement.