2614-06-4
Chemical Structure
(R)-Thalidomide
Synonym(s): (R)-(+)-Thalidomide
- CAS No.: 2614-06-4
- Formula:C13H10N2O4
- Molecular Weight:258.23
IUPAC Name: (R)-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione
InChIKey: UEJJHQNACJXSKW-SECBINFHSA-N
SMILES: O=C1N([C@H](CC2)C(NC2=O)=O)C(C3=C1C=CC=C3)=O
Biological Activity: (R)-Thalidomide ((R)-(+)-Thalidomide) is the R-enantiomer of Thalidomide (HY-14658). (R)-Thalidomide has psychomotor stabilizing properties[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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(R)-Thalidomide | 99.52% | (R)-Thalidomide ((R)-(+)-Thalidomide) is the R-enantiomer of Thalidomide (HY-14658). (R)-Thalidomide has psychomotor stabilizing properties. | ||||||||||||||||||||
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Similarity Score 1.00
HY-14658Thalidomide -
Similarity Score 1.00
HY-14658A(S)-Thalidomide -
Similarity Score 0.86
HY-139548Thalidomide-5-methyl -
Similarity Score 0.85
HY-W1005059N-Methylthalidomide -
Similarity Score 0.85
HY-W454632Thalidomide-5-Cl -
Similarity Score 0.84
HY-W586331Thalidomide-iodo -
Similarity Score 0.84
HY-W069604Thalidomide-5-Br -
Similarity Score 0.84
HY-W8677044-Me-Thalidomide -
Similarity Score 0.84
HY-W0235735-Aminothalidomide -
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References
- [1]. Murphy S, et al. Enantioselectivity of thalidomide serum and tissue concentrations in a rat glioma model and effects of combination treatment with cisplatin and BCNU. J Pharm Pharmacol. 2007 Jan;59(1):105-14. [Content Brief]
- [2]. Stephens TD, et al. Mechanism of action in thalidomide teratogenesis. Biochem Pharmacol. 2000 Jun 15;59(12):1489-99.