Date published: 2026-5-18

1-800-457-3801

SCBT Portrait Logo
Seach Input

Δ12-PGJ2 (Δ12-Prostaglandin J2) (CAS 87893-54-7)

0.0(0)
Write a reviewAsk a question

Application:
Δ12-PGJ2 (Δ12-Prostaglandin J2) is a decomposition product of PGD2 showing potent antiviral and anti-proliferative activity
CAS Number:
87893-54-7
Purity:
98%
Molecular Weight:
334.5
Molecular Formula:
C20H30O4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

Δ12-Prostaglandin J2 (Δ12-PGJ2) is a naturally occurring derivative of prostaglandin D2 (PGD2), part of a family of compounds known as prostaglandins which are involved in numerous physiological processes. This specific compound, Δ12-PGJ2, is of significant interest in biochemical research due to its unique structural properties and its role as a reactive electrophile. The mechanism of action of Δ12-PGJ2 involves its interaction with cellular proteins through a Michael addition, where the electrophilic carbon in the cyclopentenone ring of Δ12-PGJ2 forms covalent bonds with nucleophilic sites on target proteins. This interaction can modulate the function of these proteins, influencing various signaling pathways and cellular responses such as inflammation, differentiation, and apoptosis. In the research field, Δ12-PGJ2 has been utilized to study its effects on transcription factors, particularly the nuclear factor-kappa B (NF-κB) and peroxisome proliferator-activated receptor gamma (PPARγ). By modifying the activity of these transcription factors, Δ12-PGJ2 serves as a tool to explore the regulatory mechanisms behind gene expression related to inflammation and metabolic processes. Additionally, its role in modulating inflammatory responses makes Δ12-PGJ2 a valuable compound for studying the resolution phase of inflammation, where it helps to promote the cessation of inflammatory signaling and initiation of healing processes. This is particularly useful in understanding the complex dynamics of inflammation and resolution within various tissues.


Δ12-PGJ2 (Δ12-Prostaglandin J2) (CAS 87893-54-7) References

  1. Identification of cDNAs for Sox-4, an HMG-Box protein, and a novel human homolog of yeast splicing factor SSF-1 differentially regulated during apoptosis induced by prostaglandin A2/delta12-PGJ2 in Hep3B cells.  |  Ahn, SG., et al. 1999. Biochem Biophys Res Commun. 260: 216-21. PMID: 10381369
  2. Lipocalin-type and hematopoietic prostaglandin D synthases as a novel example of functional convergence.  |  Urade, Y. and Eguchi, N. 2002. Prostaglandins Other Lipid Mediat. 68-69: 375-82. PMID: 12432930
  3. Prostaglandin J2 family and the cardiovascular system.  |  Sasaguri, T. and Miwa, Y. 2004. Curr Vasc Pharmacol. 2: 103-14. PMID: 15320511
  4. Prostaglandin D2 and J2-series (PGJ2, Delta12-PGJ2) prostaglandins stimulate IL-6 and MCP-1, but inhibit leptin, expression and secretion by 3T3-L1 adipocytes.  |  Peeraully, MR., et al. 2006. Pflugers Arch. 453: 177-87. PMID: 16924534
  5. PGJ2 and delta 12PGJ2 inhibit cell growth accompanied with inhibition of phosphoinositide turnover in human astrocytoma cells.  |  Nakahata, N., et al. 1990. Prostaglandins. 40: 405-16. PMID: 2177901
  6. Conjugation of 9-deoxy-delta 9,delta 12(E)-prostaglandin D2 with intracellular glutathione and enhancement of its antiproliferative activity by glutathione depletion.  |  Atsmon, J., et al. 1990. Cancer Res. 50: 1879-85. PMID: 2306739
  7. Increased generation of cyclopentenone prostaglandins after brain ischemia and their role in aggregation of ubiquitinated proteins in neurons.  |  Liu, H., et al. 2013. Neurotox Res. 24: 191-204. PMID: 23355003
  8. Inflammatory Pathways in Knee Osteoarthritis: Potential Targets for Treatment.  |  Bar-Or, D., et al. 2015. Curr Rheumatol Rev. 11: 50-58. PMID: 26002457
  9. Site and mechanism of growth inhibition by prostaglandins. I. Active transport and intracellular accumulation of cyclopentenone prostaglandins, a reaction leading to growth inhibition.  |  Narumiya, S. and Fukushima, M. 1986. J Pharmacol Exp Ther. 239: 500-5. PMID: 3772804
  10. Conversion of prostaglandin endoperoxides to C17-hydroxy acids catalyzed by human platelet thromboxane synthase.  |  Diczfalusy, U., et al. 1977. FEBS Lett. 84: 271-4. PMID: 598509
  11. Prostaglandin A2 and delta 12-prostaglandin J2 induce apoptosis in L1210 cells.  |  Kim, IK., et al. 1993. FEBS Lett. 321: 209-14. PMID: 8477853

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Δ12-PGJ2 (Δ12-Prostaglandin J2), 500 µg

sc-201257
500 µg
$257.00

Δ12-PGJ2 (Δ12-Prostaglandin J2), 1 mg

sc-201257A
1 mg
$500.00