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thalidomide A synthetic derivative of glutamic acid (alpha-phthalimido-glutarimide) with teratogenic, immunomodulatory, anti-inflammatory and anti-angiogenic properties. Thalidomide acts primarily by inhibiting both the production of tumor necrosis factor alpha (TNF-alpha) in stimulated peripheral monocytes and the activities of interleukins and interferons. This agent also inhibits polymorphonuclear chemotaxis and monocyte phagocytosis. In addition, thalidomide inhibits pro-angiogenic factors such as vascular endothelial growth factor (VEGF) and basic fibroblast growth factor (bFGF), thereby inhibiting angiogenesis. Check for active clinical trials or closed clinical trials using this agent. (NCI Thesaurus)
Synonyms: | | alpha-phthalimidoglutarimide N-phthaloylglutamimide N-phthalylglutamic acid imide | | | US brand names: | | Synovir Thalomid | | | Foreign brand names: | | Contergan Distaval Kevadon Neurosedyn Pantosediv Sedoval K-17 Softenon Talimol | | | Abbreviation: | | THAL | | | Chemical structure names: | | - 2-(2,6-dioxo-3-piperidinyl)-1H-isoindole-1,3(2H)-dione
- 2,6-dioxo-3-phthalimidopiperidine
- 3-phthalimidoglutarimide
- N-(2,6-dioxo-3-piperidyl)phthalimide
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