T150

(−)-Thalidomide

>98%, solid

• Sinónimos: S(−)-2-(2,6-Dioxo-3-piperidinyl)-1H-isoindole-1,3(2H)-dione
• Fórmula empírica (notación de Hill): C₁₃H₁₀N₂O₄
• Número CAS: 841-67-8
• Peso molecular: 258.23
• NACRES: NA.77
• PubChem Substance ID: 24899969
• UNSPSC Code: 12352207
• MDL number: MFCD00210219
• Assay: >98%
• Form: solid

Propiedades

• ligand: thalidomide
• assay: >98%
• form: solid
• optical activity: [α]23/D −62.6°, c = 2 in DMF(lit.)
• reaction suitability: reagent type: ligand
• technique(s): cell culture | embryo: suitable
• color: white
• solubility: DMSO: soluble, H₂O: insoluble, ethanol: insoluble
• originator: Celgene
• SMILES string: O=C1CC[C@H](N2C(=O)c3ccccc3C2=O)C(=O)N1
• 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)/t9-/m0/s1
• InChI key: UEJJHQNACJXSKW-VIFPVBQESA-N
• Gene Information: human ... LITAF(9516), TNF(7124) ; mouse ... Nos2(18126) ; rat ... Nos1(24598)

Descripción

General description

Thalidomide is a stereoisomer, which exists in two enantiomeric states. The S enantiomer is teratogenic. Thalidomide consists of two linked rings, a phthalimide and glutarimide ring.

Application

Thalidomide has been used to study its teratogenic effects in chicken embryos and human embryonic cells. This study reported that thalidomide causes limb defects by stabilizing PTEN, inhibiting the expression of Akt and activating caspase-dependent apoptosis[1]. Thalidomide has also been used for studying glutathione mediated teratogenic resistance in mouse embryos[2].

Biochem/physiol Actions

(-)-Thalidomide selectively inhibits the biosynthesis of tumor necrosis factor α (TNF-α), which is essential for inflammatory response. It is an anti-emetic drug and is used to treat morning sickness in pregnant women. Thalidomide is also used to treat leprosy, multiple myeloma, Crohn′s disease and human immunodeficiency virus (HIV) infection. Thalidomide also inhibits angiogenesis. It is associated with several diseases such as, peripheral neuropathy, facial palsies, Duane syndrome and autism.

Features and Benefits

This compound was developed by Celgene. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

Preparation Note

(-)-Thalidomide is soluble in DMSO, but is insoluble in water and ethanol.

Información de seguridad

• pictograms: GHS08,GHS07
• signalword: Danger
• hcodes: H302,H360
• pcodes: P201 - P301 + P312 + P330 - P308 + P313
• Hazard Classifications: Acute Tox. 4 Oral - Repr. 1B
• Clase de almacenamiento: 6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
• wgk: WGK 3
• ppe: Eyeshields, Gloves, type P3 (EN 143) respirator cartridges