Descriptor English: | Thalidomide | ||||
Descriptor Spanish: |
Talidomida
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Descriptor Portuguese: | Talidomida | ||||
Descriptor French: | Thalidomide | ||||
Entry term(s): |
Sedoval Thalomid |
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Tree number(s): |
D02.241.223.805.810.800 D03.383.621.808.800 D03.633.100.513.750.750 |
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RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D013792 | ||||
Scope note: | A piperidinyl isoindole originally introduced as a non-barbiturate hypnotic, but withdrawn from the market due to teratogenic effects.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. |
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Allowable Qualifiers: |
AA analogs & derivatives AD administration & dosage AE adverse effects AG agonists AI antagonists & inhibitors AN analysis BL blood CF cerebrospinal fluid CH chemistry CL classification CS chemical synthesis EC economics HI history IM immunology IP isolation & purification ME metabolism PD pharmacology PK pharmacokinetics PO poisoning RE radiation effects SD supply & distribution ST standards TO toxicity TU therapeutic use UR urine |
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Pharm Action: |
Immunosuppressive Agents Leprostatic Agents Teratogens Angiogenesis Inhibitors |
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Registry Number: | 4Z8R6ORS6L | ||||
CAS Type 1 Name: | 1H-Isoindole-1,3(2H)-dione, 2-(2,6-dioxo-3-piperidinyl)- | ||||
DeCS ID: | 14171 | ||||
Unique ID: | D013792 | ||||
Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||
Date Established: | 1966/01/01 | ||||
Date of Entry: | 1999/01/01 | ||||
Revision Date: | 2017/05/24 |
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CHEMICALS AND DRUGS
Organic Chemicals [D02]Organic Chemicals -
CHEMICALS AND DRUGS
Heterocyclic Compounds [D03]Heterocyclic Compounds -
CHEMICALS AND DRUGS
Heterocyclic Compounds [D03]Heterocyclic Compounds
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Thalidomide
- Preferred
Sedoval
- Narrower
Thalomid
- Narrower
Concept UI |
M0021267 |
Scope note | 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. |
Preferred term | Thalidomide |
Concept UI |
M0332437 |
Preferred term | Sedoval |
Concept UI |
M0476424 |
Preferred term | Thalomid |
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