Description
Cell-permeable. A teratogen and sedative-hypnotic with inherent anti-inflammatory properties. A selective inhibitor of tumor necrosis factor α (TNF-α) synthesis. Thalidomide initiates its teratogenic effects by binding to cereblon (CRBN), a thalidomide-binding protein, and inhibiting the associated ubiquitin ligase activity.
(±)-Thalidomide is a teratogen and sedative-hypnotic with inherent anti-inflammatory properties. A selective inhibitor of tumor necrosis factor α (TNF-α) synthesis. Thalidomide initiates its teratogenic effects by binding to cereblon (CRBN), a thalidomide-binding protein, and inhibiting the associated ubiquitin ligase activity.
2020 | (±)-Thalidomide DataSheet
Alternate Name/Synonyms: (RS)-2-(2,6-dioxopiperidin-3-yl)-1H-isoindole-1,3(2H)-dione
Appearance: White solid
Formulation: N/A
CAS Number: 50-35-1
Structure Available?: Yes
Peptide sequence: N/A
Salt Form: No
Molecular Formula: C₁₃H₁₀N₂O₄
Molecular Weight: 258.23
Cell-Permeable?: Yes
Purity: ≥98% by TLC
Solubilities: DMSO (5 mg/ml)
Handling: Protect from air and light
Country of Origin: USA
Tag Line: A selective inhibitor of tumor necrosis factor α (TNF-α) synthesis
MDL Number: MFCD00153873
PubChem CID: 5426
SMILES: C1CC(=O)NC(=O)C1N2C(=O)C3=CC=CC=C3C2=O
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: UEJJHQNACJXSKW-UHFFFAOYSA-N
Additional Information
Storage Condition: |
-20°C |
Shipping Condition: |
Gel Pack |
Shelf Life: |
24 months |