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rdf:type
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http://linked.open...gbank/description
| - A piperidinyl isoindole originally introduced as a non-barbiturate hypnotic, but withdrawn from the market due to teratogenic effects.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 immunosuppresive and anti-angiogenic activity. It inhibits release of tumor necrosis factor-alpha from monocytes, and modulates other cytokine action. [PubChem] (en)
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http://linked.open...y/drugbank/dosage
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http://linked.open...gy/drugbank/group
| - approved (en)
- withdrawn (en)
- investigational (en)
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http://linked.open...drugbank/halfLife
| - The mean half-life of elimination ranges from approximately 5 to 7 hours following a single dose and is not altered upon multiple dosing. (en)
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http://linked.open...ugbank/indication
| - For the acute treatment of the cutaneous manifestations of moderate to severe erythema nodosum leprosum (ENL). Also for use as maintenance therapy for prevention and suppression of the cutaneous manifestations of ENL recurrence. (en)
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sameAs
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Title
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adms:identifier
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http://linked.open...mechanismOfAction
| - In patients with erythema nodosum leprosum (ENL) the mechanism of action is not fully understood. Available data from in vitro studies and preliminary clinical trials suggest that the immunologic effects of this compound can vary substantially under different conditions, but may be related to suppression of excessive tumor necrosis factor-alpha (TNF-a) production and down-modulation of selected cell surface adhesion molecules involved in leukocyte migration. For example, administration of thalidomide has been reported to decrease circulating levels of TNF-a in patients with ENL, however, it has also been shown to increase plasma TNF-a levels in HIV-seropositive patients. As a cancer treatment, the drug may act as a VEGF inhibitor. (en)
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http://linked.open...drugbank/packager
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http://linked.open...y/drugbank/patent
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http://linked.open...outeOfElimination
| - Thalidomide itself has less than 0.7% of the dose excreted in the urine as unchanged drug. (en)
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http://linked.open.../drugbank/synonym
| - Thalidomide (en)
- Distaval (en)
- Pro-ban M (en)
- Sedalis (en)
- Softenon (en)
- Talimol (en)
- N-Phthaloylglutamimide (en)
- N-Phthalylglutamic acid imide (en)
- (+-)-N-(2,6-dioxo-3-Piperidyl)phthalimide (en)
- (+-)-Thalidomide (en)
- (±)-N-(2,6-dioxo-3-piperidyl)phthalimide (en)
- (±)-thalidomide (en)
- 1,3-dioxo-2-(2,6-dioxopiperidin-3-yl)isoindoline (en)
- 2,6-dioxo-3-phthalimidopiperidine (en)
- 3-Phthalimidoglutarimide (en)
- K-17 (en)
- N-(2,6-dioxo-3-piperidyl)phthalimide (en)
- N-Phthalyl-glutaminsaeure-imid (en)
- Talidomida (en)
- Thalidomidum (en)
- alpha-(N-Phthalimido)glutarimide (en)
- alpha-N-Phthalylglutaramide (en)
- alpha-Phthalimidoglutarimide (en)
- α-(N-phthalimido)glutarimide (en)
- α-N-phthalylglutaramide (en)
- α-phthalimidoglutarimide (en)
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http://linked.open...drugbank/toxicity
| - The R-configuration and the S-configuration are more toxic individually than the racemic mixture. The LD<sub>50</sub> could not be established in mice for racemic thalidomide, whereas LD<sub>50</sub> values for the R and S configurations are reported to be 0.4 to 0.7 g/kg and 0.5 to 1.5 g/kg, respectively. (en)
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http://linked.open...nk/proteinBinding
| - 55% and 66% for the (+)R and (−)S enantiomers, respectively. (en)
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http://linked.open...ynthesisReference
| - Jamshed Shah, "Synthesis and anti-tumor activity of nitrogen substituted thalidomide analogs." U.S. Patent US20030139451, issued July 24, 2003. (en)
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http://linked.open...y/mesh/hasConcept
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foaf:page
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http://linked.open...ugbank/IUPAC-Name
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http://linked.open...gy/drugbank/InChI
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http://linked.open...Molecular-Formula
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http://linked.open.../Molecular-Weight
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http://linked.open...noisotopic-Weight
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http://linked.open...y/drugbank/SMILES
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http://linked.open.../Water-Solubility
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http://linked.open...ogy/drugbank/logP
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http://linked.open...ogy/drugbank/logS
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http://linked.open...l/drug/hasATCCode
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http://linked.open...nd-Acceptor-Count
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http://linked.open...-Bond-Donor-Count
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http://linked.open...drugbank/InChIKey
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http://linked.open...urface-Area--PSA-
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http://linked.open...nk/Polarizability
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http://linked.open...bank/Refractivity
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http://linked.open...atable-Bond-Count
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http://linked.open...ugbank/absorption
| - The absolute bioavailability has not yet been characterized in human subjects due to its poor aqueous solubility. In studies of both healthy volunteers and subjects with Hansen’s disease, the mean time to peak plasma concentrations (Tmax) ranged from 2.9 to 5.7 hours indicating that thalidomide is slowly absorbed from the gastrointestinal tract. (en)
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http://linked.open.../affectedOrganism
| - Humans and other mammals (en)
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http://linked.open...casRegistryNumber
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http://linked.open...drugbank/category
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http://linked.open...gbank/containedIn
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http://linked.open...k/Bioavailability
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http://linked.open...bank/Ghose-Filter
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http://linked.open...nk/MDDR-Like-Rule
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http://linked.open...ank/Melting-Point
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http://linked.open...k/Number-of-Rings
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http://linked.open...siological-Charge
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