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Taprostene (CAS 108945-35-3)

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Alternate Names:
Rheocyclan; CG 4203
Application:
Taprostene is a highly selective agonist of the prostanoid receptor IP1
CAS Number:
108945-35-3
Purity:
≥95%
Molecular Weight:
398.49
Molecular Formula:
C24H30O5
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Taprostene, a synthetic derivative of prostaglandin E2 (PGE2), has been a subject of extensive research primarily within the realm of inflammation and immunology. One prominent area of investigation is its role as a modulator of immune responses, particularly in the context of inflammatory diseases. Studies have explaind taprostene′s mechanism of action, revealing its ability to interact with specific prostaglandin receptors, such as EP2 and EP4, on immune cells. Through these interactions, taprostene exerts regulatory effects on various signaling pathways involved in inflammation, including the NF-κB and MAPK pathways, leading to modulation of cytokine production and immune cell function. Moreover, taprostene has been explored for its potential applications in models of inflammatory disorders, such as rheumatoid arthritis and inflammatory bowel disease. Research efforts have aimed to further explain the precise molecular mechanisms underlying taprostene′s immunomodulatory effects and to evaluate its efficacy and safety for interventions targeting dysregulated immune responses. Additionally, investigations into taprostene′s pharmacokinetics and pharmacodynamics have provided valuable insights into its bioavailability, distribution, and metabolism, facilitating the development of optimized dosing regimens for experimental studies and potential clinical translation in the future.


Taprostene (CAS 108945-35-3) References

  1. Effects of PGI2 and analogues (taprostene, iloprost) on oxidation of native and glycated LDL.  |  Sobal, G. and Sinzinger, H. 1999. Life Sci. 65: 1237-46. PMID: 10503939
  2. Effect of cerebrocrast on the function of human platelets and release of the arachidonic acid from plasma membrane.  |  Briede, J., et al. 2002. Cell Biochem Funct. 20: 177-81. PMID: 11979514
  3. Investigation of the agonist activity of prostacyclin analogues on prostanoid EP4 receptors using GW 627368 and taprostene: evidence for species differences.  |  Jones, RL. and Chan, KM. 2005. Prostaglandins Leukot Essent Fatty Acids. 72: 289-99. PMID: 15763441
  4. Selective prostacyclin receptor agonism augments glucocorticoid-induced gene expression in human bronchial epithelial cells.  |  Wilson, SM., et al. 2009. J Immunol. 183: 6788-99. PMID: 19880449
  5. Taprostene, a stable prostacyclin analogue, enhances the thrombolytic efficacy of saruplase (recombinant single-chain urokinase-type plasminogen activator) in rabbits with pulmonary embolized thrombi.  |  Schneider, J. 1991. Prostaglandins. 41: 595-606. PMID: 2052741
  6. Effects of taprostene, a stable prostacyclin analogue, on haemodynamics, platelet function and arachidonate metabolism in healthy volunteers.  |  Virgolini, I., et al. 1990. Eur J Clin Pharmacol. 38: 347-50. PMID: 2111774
  7. The prostacyclin analogue taprostene and recombinant human superoxide dismutase increase the permanent survival rate of endotoxemic rats.  |  Schneider, J. and Matthiesen, T. 1990. Life Sci. 46: 1421-6. PMID: 2111867
  8. Evidence for a second receptor for prostacyclin on human airway epithelial cells that mediates inhibition of CXCL9 and CXCL10 release.  |  Wilson, SM., et al. 2011. Mol Pharmacol. 79: 586-95. PMID: 21173040
  9. Endothelium and myocardial protecting actions of taprostene, a stable prostacyclin analogue, after acute myocardial ischemia and reperfusion in cats.  |  Johnson, G., et al. 1990. Circ Res. 66: 1362-70. PMID: 2159389
  10. Additional myocardial salvage by coadministration of the epoprostenol analog taprostene to recombinant single-chain urokinase-type plasminogen activator in a canine coronary thrombosis model.  |  Groves, R., et al. 1989. Arzneimittelforschung. 39: 534-8. PMID: 2665759
  11. The effect of taprostene in patients with acute myocardial infarction treated with thrombolytic therapy: results of the START study. Saruplase Taprostene Acute Reocclusion Trial.  |  Bär, FW., et al. 1993. Eur Heart J. 14: 1118-26. PMID: 8404943
  12. [The effect of Taprostene on platelet activation and clinical course after percutaneous transluminal angioplasty].  |  Heinz, M., et al. 1996. Vasa. 25: 65-72. PMID: 8851268

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Taprostene, 1 mg

sc-215940
1 mg
$179.00

Taprostene, 5 mg

sc-215940A
5 mg
$645.00