Thalidomide FDA Link

A piperidinyl isoindole originally introduced as a non-barbiturate hypnotic, but withdrawn from the market due to teratogenic effects. It has been reintroduced and used for a number of immunological and inflammatory disorders. Thalidomide displays immunosuppressive and anti-angiogenic activity. It inhibits release of TUMOR NECROSIS FACTOR-ALPHA from monocytes, and modulates other cytokine action.

Also Known As:

Thalomid; Sedoval; 1H-Isoindole-1,3(2H)-dione, 2-(2,6-dioxo-3-piperidinyl)-

Pharmalogical Action Categories:

Angiogenesis Inhibitors
Immunosuppressive Agents
Leprostatic Agents
Teratogens

Organic Chemicals: 140
- Carboxylic Acids: 986
  - Carbocyclic Acids
    - Phthalic Acids: 1
      - Phthalimides: 14
        Thalidomide: 4742
Heterocyclic Compounds: 207
- 1-Ring Heterocyclic Compounds
  - Piperidines: 17
    - Piperidones: 39
      - Thalidomide: 4742
- Fused-Ring Heterocyclic Compounds
  - 2-Ring Heterocyclic Compounds
    - Isoindoles: 20
      - Phthalimides: 14
        Thalidomide: 4742

Ruth Wadman Selected Research

Ruth Wadman Research Topics

Disease

Drug/Important Bio-Agent (IBA)