Date published: 2026-5-24

1-800-457-3801

SCBT Portrait Logo
Seach Input

(R)-(+)-Thalidomide (CAS 2614-06-4)

0.0(0)
Write a reviewAsk a question

Alternate Names:
(R)-Thalidomide
Application:
(R)-(+)-Thalidomide is one isomer of the antiangiogenic Thalidomide
CAS Number:
2614-06-4
Purity:
≥98%
Molecular Weight:
258.23
Molecular Formula:
C13H10N2O4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

(R)-(+)-Thalidomide is one of the enantiomers of thalidomide, a compound that has been widely studied due to its interesting chemical and biological properties. The (R)-enantiomer of thalidomide has been a subject of extensive research in the field of chirality and its effects on biological activity. R)-(+)-Thalidomide has been examined for its ability to modulate the immune system and influence the production of various cytokines and growth factors. This compound has been found to selectively inhibit the production of tumor necrosis factor alpha (TNF-α), a critical cytokine involved in systemic inflammation and a key target in studies of inflammatory diseases. Researchers explore how this modulation occurs by investigating the binding of (R)-(+)-Thalidomide to the cereblon complex, a part of the ubiquitin ligase complex, affecting the degradation of specific transcription factors. Beyond immunomodulation, (R)-(+)-Thalidomide has been used in research to understand its effects on cellular mechanisms like angiogenesis. The compound′s ability to inhibit the formation of new blood vessels under certain conditions is linked to its impact on vascular endothelial growth factor (VEGF) and basic fibroblast growth factor (bFGF) pathways. (R)-(+)-Thalidomide is also a valuable tool in chiral chemistry research, particularly in studying the mechanisms behind the differential biological activities of enantiomers. It helps in understanding how the stereochemistry of a molecule influences its interaction with various biological targets.


(R)-(+)-Thalidomide (CAS 2614-06-4) References

  1. Investigation of the in vitro biotransformation of R-(+)-thalidomide by HPLC, nano-HPLC, CEC and HPLC--APCI-MS.  |  Meyring, M., et al. 1999. J Chromatogr B Biomed Sci Appl. 723: 255-64. PMID: 10080653
  2. Modified DNA aptamer that binds the (R)-isomer of a thalidomide derivative with high enantioselectivity.  |  Shoji, A., et al. 2007. J Am Chem Soc. 129: 1456-64. PMID: 17263432
  3. Recent advances in analytical determination of thalidomide and its metabolites.  |  Bosch, ME., et al. 2008. J Pharm Biomed Anal. 46: 9-17. PMID: 18023317
  4. Teratogenic effects of thalidomide: molecular mechanisms.  |  Ito, T., et al. 2011. Cell Mol Life Sci. 68: 1569-79. PMID: 21207098
  5. Enantiomerization mechanism of thalidomide and the role of water and hydroxide ions.  |  Tian, C., et al. 2012. Chemistry. 18: 14305-13. PMID: 23065668
  6. A Mini-Review on Thalidomide: Chemistry, Mechanisms of Action, Therapeutic Potential and Anti-Angiogenic Properties in Multiple Myeloma.  |  Mercurio, A., et al. 2017. Curr Med Chem. 24: 2736-2744. PMID: 28571559
  7. A comparison of the teratogenic activity of thalidomide in rabbits and rats.  |  Schumacher, H., et al. 1968. J Pharmacol Exp Ther. 160: 189-200. PMID: 5639104
  8. Thalidomide is an inhibitor of angiogenesis.  |  D'Amato, RJ., et al. 1994. Proc Natl Acad Sci U S A. 91: 4082-5. PMID: 7513432
  9. Thalidomide inhibits the replication of human immunodeficiency virus type 1.  |  Makonkawkeyoon, S., et al. 1993. Proc Natl Acad Sci U S A. 90: 5974-8. PMID: 8327469

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

(R)-(+)-Thalidomide, 10 mg

sc-208224
10 mg
$183.00