CAS 50-35-1
:Thalidomide
Description:
Thalidomide, with the CAS number 50-35-1, is a synthetic compound originally developed in the late 1950s as a sedative and later prescribed for morning sickness in pregnant women. It is classified as a phthalimide derivative and has a molecular formula of C13H10N2O4. Thalidomide is known for its unique mechanism of action, which includes immunomodulatory effects, anti-inflammatory properties, and inhibition of angiogenesis. Its structure features a chiral center, leading to two enantiomers, one of which is associated with the drug's therapeutic effects, while the other is linked to severe teratogenic effects, resulting in birth defects when taken during pregnancy. Due to these risks, thalidomide was withdrawn from the market in the early 1960s. However, it has since been repurposed and is now used under strict regulations for the treatment of certain conditions, such as multiple myeloma and leprosy-related complications. Its use is closely monitored due to its potential side effects, including peripheral neuropathy and thromboembolic events.
Formula:C13H10N2O4
InChI:InChI=1S/C13H10N2O4/c16-10-6-5-9(11(17)14-10)15-12(18)7-3-1-2-4-8(7)13(15)19/h1-4,9H,5-6H2,(H,14,16,17)
InChI key:InChIKey=UEJJHQNACJXSKW-UHFFFAOYSA-N
SMILES:O=C1N(C(=O)C=2C1=CC=CC2)C3C(=O)NC(=O)CC3
Synonyms:- 1,3-Dioxo-2-(2,6-dioxopiperidin-3-yl)isoindoline
- 1H-Isoindole-1,3(2H)-dione, 2-(2,6-dioxo-3-piperidinyl)-
- 2-(2,6-Dioxo-3-Piperidinyl)-1H-Isoindole-1,3(2H)-Dione
- 2-(2,6-Dioxo-piperidin-3-yl)-isoindole-1,3-dione
- 2-(2,6-Dioxopiperidin-3-yl)-2,3-dihydro-1H-isoindole-1,3-dione
- 2-(2,6-Dioxopiperidin-3-yl)isoindole-1,3-dione
- 2-(2,6-Dioxopiperidin-3-yl)isoindoline-1,3-dione
- 2-(2,6-dioxopiperidin-3-yl)-1H-isoindole-1,3(2H)-dione
- 2-Phthalimidoglutarimide
- 3-Phthalimidoglutarimide
- Celgene
- Contergan
- Distaval
- Immunoprin
- K 17
- Kevadon
- Myrin
- N-(2,6-Dioxo-3-piperidinyl)phthalimide
- N-(2,6-Dioxo-3-piperidyl)phthalimide
- N-Phthaloylglutamimide
- Neurosedyn
- Nsc 527179
- Nsc 66847
- Pantosediv
- Pharmion
- Phthalimide, N-(2,6-dioxo-3-piperidyl)-
- Quetimid
- Sauramide
- Sedalis
- Sedoval
- Softenil
- Softenon
- Suaramide
- Synovir
- Talidomida
- Talimol
- Talinol
- Thaled
- Thalidomid
- Thalomid
- α-(N-Phthalimido)glutarimide
- α-N-Phthalylglutaramide
- See more synonyms
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Found 18 products.
(±)-Thalidomide
CAS:Formula:C13H10N2O4Purity:>98.0%(HPLC)(N)Color and Shape:White to Almost white powder to crystalMolecular weight:258.23(+/-)-Thalidomide, 99+%
CAS:<p>Teratogenic compound found to inhibit HIV-1 replication and FGF-induced angiogenesis</p>Formula:C13H10N2O4Purity:99+%Color and Shape:White to cream, PowderMolecular weight:258.23Thalidomide
CAS:<p>Teratogenic compound found to inhibit HIV-1 replication and FGF-induced angiogenesis</p>Formula:C13H10N2O4Molecular weight:258.23Thalidomide
CAS:<p>Imides and their derivatives (excluding sacharin), and salts thereof</p>Formula:C13H10N2O4Color and Shape:White Off-White PowderMolecular weight:258.06406Thalidomide
CAS:<p>Thalidomide, a glutamic acid derivative, has teratogenic and immunomodulatory effects.</p>Formula:C13H10N2O4Purity:98.88% - 99.88%Color and Shape:White SolidMolecular weight:258.23Thalidomide-d4
CAS:Formula:C13H6D4N2O4Color and Shape:White To Off-White SolidMolecular weight:262.26Thalidomide
CAS:Formula:C13H10N2O4Purity:≤ 0.1%Color and Shape:White to off-white powderMolecular weight:258.23(+/-)-Thalidomide - Bio-X ™
CAS:Controlled Product<p>Thalidomide is a piperidinyl isoindole drug that is used to treat various cancers such as myeloma and erythema nodosum leprosum. This drug is immunosuppressive and has anti-angiogenic activity. Thalidomide’s mechanism of action is not fully understood however it is thought to block the activity of tumor necrosis factor-alpha (TNF-α).</p>Formula:C13H10N2O4Purity:Min. 95%Color and Shape:PowderMolecular weight:258.23 g/mol(+/-)-Thalidomide
CAS:Controlled Product<p>Classified as immunomodulatory drug, thalidomide suppresses the expression of tumor necrosis factor-alpha (TNF-α), interferes with a cascade of pro-inflammatory cytokines, and interferes with the secretion of vascular endothelial growth factor (VEGF) and beta fibroblast growth factor (bFGF). Similarly to apremilast, thalidomide carries a phthalimide ring, together with a glutarimide ring that is specifically recognized by the target molecule cereblon. Thanks to its ability to contrast neoangiogenesis and the modifications of the bone marrow stromal microenvironment, thalidomide is a powerful tool to fight hematologic cancers. In the treatment of SARS-CoV-2, the immunomodulatory and anti-inflammatory action of thalidomide has and has proved beneficial when combined with a low-dose glucocorticoid.</p>Formula:C13H10N2O4Purity:Min. 95%Color and Shape:White PowderMolecular weight:258.23 g/mol(+/-)-Thalidomide
CAS:<p>M02554 - (+/-)-Thalidomide</p>Formula:C13H10N2O4Purity:98%Color and Shape:SolidMolecular weight:258.233Thalidomide
CAS:Controlled Product<p>Applications Inhibits FGF-induced angiogenesis. Inhibits replication of human immunodeficiency virus type 1. Teratogenic sedative. There is now a growing clinical interest in Thalidomide, and it is introduced as an immunomodulatory agent used primarily in combination with dexamethasone to treat multiple myeloma.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References D’Amato, r.J., et al.: Proc. Natl. Acad. Sci. USA, 91, 4082 (1994), Makonkawkeyoon, S., et al.: Proc. Natl. Acad. Sci. USA, 90, 5974 (1993), Schumacher, H., et al.: J. Pharmacol. Exp. Therap., 160, 189 (1968)<br></p>Formula:C13H10N2O4Color and Shape:NeatMolecular weight:258.23













