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Etodolac (CAS 41340-25-4)

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Alternate Names:
Etodolic acid; Etogesic; Lodine; Tedolan; Ultradol
Application:
Etodolac is a Cox-2 inhibitor with anti-inflammatory activity
CAS Number:
41340-25-4
Purity:
≥98%
Molecular Weight:
287.35
Molecular Formula:
C17H21NO3
Supplemental Information:
This is 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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Etodolac is a nonsteroidal anti-inflammatory compound that functions as an inhibitor of the enzyme cyclooxygenase (COX). It specifically inhibits the COX-2 enzyme, which is responsible for the production of prostaglandins involved in inflammation and pain. By blocking the action of COX-2, etodolac reduces the synthesis of prostaglandins, thereby decreasing inflammation and pain. This chemical′s mode of action involves binding to the active site of the COX-2 enzyme, preventing the conversion of arachidonic acid into prostaglandins. This inhibition of prostaglandin synthesis contributes to the anti-inflammatory and analgesic effects of etodolac. Additionally, etodolac may act to have some selectivity for COX-2 over COX-1, which may contribute to its reduced gastrointestinal side effects compared to other NSAIDs. Overall, etodolac′s function as a COX-2 inhibitor makes it a useful tool for studying the role of prostaglandins in inflammation and pain pathways at the molecular level.


Etodolac (CAS 41340-25-4) References

  1. Etodolac inhibits EBER expression and induces Bcl-2-regulated apoptosis in Burkitt's lymphoma cells.  |  Kobayashi, M., et al. 2005. Eur J Haematol. 75: 212-20. PMID: 16104877
  2. Etodolac. A reappraisal of its pharmacology and therapeutic use in rheumatic diseases and pain states.  |  Balfour, JA. and Buckley, MM. 1991. Drugs. 42: 274-99. PMID: 1717225
  3. Etodolac attenuates mechanical allodynia in a mouse model of neuropathic pain.  |  Inoue, N., et al. 2009. J Pharmacol Sci. 109: 600-5. PMID: 19346674
  4. Etodolac: efficacy in osteoarthritis and effects on chondrocyte function.  |  Bacon, PA. 1990. Rheumatol Int. 10 Suppl: 3-7. PMID: 2150570
  5. Etodolac blocks the allyl isothiocyanate-induced response in mouse sensory neurons by selective TRPA1 activation.  |  Inoue, N., et al. 2012. Pharmacology. 90: 47-54. PMID: 22739568
  6. Etodolac activates and desensitizes transient receptor potential ankyrin 1.  |  Wang, S., et al. 2013. J Neurosci Res. 91: 1591-8. PMID: 24027177
  7. Etodolac. A preliminary review of its pharmacodynamic activity and therapeutic use.  |  Lynch, S. and Brogden, RN. 1986. Drugs. 31: 288-300. PMID: 2940079
  8. Pharmacokinetic modeling and simulation of etodolac following single oral administration in dogs.  |  Baek, IH. 2019. Xenobiotica. 49: 981-986. PMID: 30216103
  9. Improved degradation of etodolac in the presence of core-shell ZnFe2O4/SiO2/TiO2 magnetic photocatalyst.  |  Mrotek, E., et al. 2020. Sci Total Environ. 724: 138167. PMID: 32251886
  10. Transfersome Hydrogel Containing 5-Fluorouracil and Etodolac Combination for Synergistic Oral Cancer Treatment.  |  Bollareddy, SR., et al. 2022. AAPS PharmSciTech. 23: 70. PMID: 35132496
  11. Etodolac Enhances the Radiosensitivity of Irradiated HT-29 Human Colorectal Cancer Cells.  |  Shaghaghi, Z., et al. 2022. Curr Radiopharm. 15: 242-248. PMID: 35319403
  12. Cardiovascular Risks of Diclofenac Versus Other Older COX-2 Inhibitors (Meloxicam and Etodolac) and Newer COX-2 Inhibitors (Celecoxib and Etoricoxib): A Series of Nationwide Emulated Trials.  |  Schmidt, M., et al. 2022. Drug Saf. 45: 983-994. PMID: 35909207
  13. Application of ionic liquid to enhance the nose-to-brain delivery of etodolac.  |  Tanigawa, H., et al. 2022. Eur J Pharm Sci. 178: 106290. PMID: 36058500

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Etodolac, 100 mg

sc-204747
100 mg
$89.00
US: (Out of Stock: Availability February 11, 2026)

Etodolac, 250 mg

sc-204747A
250 mg
$131.00

What is the solubility of this product?

Asked by: hawkeye11
This product is soluble in DMSO (100 mM), and ethanol (100 mM)
Answered by: Tech Service 4
Date published: 2016-12-16
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Rated 5 out of 5 by from Ishiguro et alIshiguro et al. (PubMed ID 25797973) used the selective cyclooxygenase-2 inhibitor with anti-inflammatory activity, etodolac, to treat post-operative pain. -SCBT Publication Review
Date published: 2015-04-14
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Etodolac | CAS 41340-25-4 is rated 5.0 out of 5 by 1.
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