Date published: 2025-10-19

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(8R,12R,11R,16RS)-Misoprostol-d5

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Alternate Names:
(11α,13E)-11,16-Dihydroxy-16-methyl-9-oxoprost-13-en-1-oic Acid-d5 Methyl Ester
Application:
(8R,12R,11R,16RS)-Misoprostol-d5 is a deuterated version of PGE1 with agonist activity mediated by EP2, EP3, and EP4
Molecular Weight:
387.56
Molecular Formula:
C22H33D5O5
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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(8R,12R,11R,16RS)-Misoprostol-d5 is a deuterated version of misoprostol, where five hydrogen atoms are replaced by deuterium, a stable isotope of hydrogen. This modification is primarily used in research to study the pharmacokinetics and metabolic pathways of misoprostol without the intent for therapeutic applications. The presence of deuterium atoms slows the rate of metabolic degradation due to the kinetic isotope effect, where bonds involving deuterium are more difficult to break compared to those with hydrogen. This results in a more prolonged interaction of the compound within biological systems, which can be crucial for detailed metabolic studies. By using (8R,12R,11R,16RS)-Misoprostol-d5 in research, scientists can trace and understand the behavior of misoprostol in various biological contexts with greater accuracy, observing how it interacts with different enzymes and what metabolic pathways it undergoes in a more controlled manner. This type of study is critical for elucidating the mechanisms of action of the parent compound at a molecular level, providing insights into its biochemical interactions and transformations without directly implicating clinical or therapeutic contexts. Moreover, this research contributes significantly to the fields of synthetic and analytical chemistry, where such isotopically labeled compounds are indispensable tools.


(8R,12R,11R,16RS)-Misoprostol-d5 References

  1. Prevention of NSAID-induced gastric ulcer with misoprostol: multicentre, double-blind, placebo-controlled trial.  |  Graham, DY., et al. 1988. Lancet. 2: 1277-80. PMID: 2904006
  2. Intravaginal misoprostol versus dinoprostone as cervical ripening and labor-inducing agents.  |  Fletcher, H., et al. 1994. Obstet Gynecol. 83: 244-7. PMID: 8290188
  3. Duodenal and gastric ulcer prevention with misoprostol in arthritis patients taking NSAIDs. Misoprostol Study Group.  |  Graham, DY., et al. 1993. Ann Intern Med. 119: 257-62. PMID: 8328732

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

(8R,12R,11R,16RS)-Misoprostol-d5, 1 mg

sc-217514
1 mg
$350.00