Date published: 2025-10-14

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L-Idaric Acid (CAS 80876-58-0)

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CAS Number:
80876-58-0
Molecular Weight:
210.14
Molecular Formula:
C6H10O8
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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L-Idaric Acid, a naturally occurring compound, has garnered attention in research for its potential applications. Recent studies have explaind its mechanism of action, revealing its involvement in modulating various cellular pathways. Research indicates that L-Idaric Acid acts as an inhibitor of certain enzymes involved in key metabolic processes, particularly those related to carbohydrate metabolism and energy production. By inhibiting these enzymes, L-Idaric Acid disrupts metabolic pathways, leading to alterations in cellular metabolism and energy homeostasis. Additionally, investigations have shown that L-Idaric Acid exhibits antioxidant properties, scavenging reactive oxygen species (ROS) and mitigating oxidative stress-induced damage in cells. Furthermore, research suggests its role in regulating immune responses and inflammation, potentially through modulation of signaling pathways involved in immune cell activation and cytokine production. Beyond its cellular effects, L-Idaric Acid has been explored for its potential applications in various disease conditions, including metabolic disorders, neurodegenerative diseases, and inflammatory disorders. Its multifaceted mechanisms of action make L-Idaric Acid a promising candidate for further research and development in biomedical sciences.


L-Idaric Acid (CAS 80876-58-0) References

  1. BIOSYNTHESIS OF MYO-INOSITOL IN RAT SEMINAL VESICLES AND PROSTATES.  |  IMAI, Y. 1964. J Biochem. 55: 126-30. PMID: 14140992
  2. Synthesis of L-idaro-1,4-lactone, an inhibitor of alpha-L-idosiduronase.  |  Herd, JK., et al. 1982. Carbohydr Res. 99: 33-9. PMID: 7055824
  3. Synthesis of l-iduronic acid derivatives by epimerisation of anancomeric d-glucuronic acid analogues.  |  Baggett, Neil, and Alan Smithson. 1982. Carbohydrate Research. 108.1: 59-70.
  4. Impact of the central hydroxyl groups on the activity of symmetrical HIV-1 protease inhibitors derived from L-mannaric acid.  |  Wachtmeister, Johanna, ]. 2000. Tetrahedron. 56.20: 3219-3225.
  5. Syntheses of l-iduronyl synthons. A review.'  |  Pellissier, Hélène. ". 2002. Organic preparations and procedures international. 34.5: 441-465.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

L-Idaric Acid, 5 mg

sc-221806
5 mg
$330.00