Chemistry:Otilonium bromide

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Short description: Chemical compound
Otilonium bromide
Otilonium bromide.png
Clinical data
Trade namesSpasmoctyl 40, Doralin
AHFS/Drugs.comInternational Drug Names
ATC code
Identifiers
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
Chemical and physical data
FormulaC29H43BrN2O4
Molar mass563.577 g·mol−1
3D model (JSmol)
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Otilonium bromide, sold under the trade name Spasmomen among others, is an antimuscarinic and calcium channel blocker used to relieve spasmodic pain of the gut, especially in irritable bowel syndrome.[1] This means it works in the gut themselves, by relaxing the small muscles of the intestines, which results in relieving cramps and therefore reduces pain.

Medical uses

A pooled analysis of three clinical trials suggest that otilonium is more effective than placebo for the treatment of irritable bowel syndrome.[2]

Pharmacology

Otilinium binds to both muscarinic receptors and tachykinin NK2 receptors.[3] It has been shown to inhibit L-type and T-type calcium channels, actions which may contribute to or determine its effects in the gut.[4][5]

When taken orally, very little of the drug is absorbed into the rest of the body,[6] which means that most of its actions remain confined to the gastrointestinal system.

References

  1. "Dismox". http://www.grupounipharm.com/sites/default/files/DISMOX+Inserto+CORREGIDO+2011.+Ingl%C3%A9s.pdf. 
  2. "Efficacy of otilonium bromide in irritable bowel syndrome: a pooled analysis". Therapeutic Advances in Gastroenterology 10 (3): 311–322. March 2017. doi:10.1177/1756283X16681708. PMID 28246548. 
  3. "Otilonium bromide: a selective spasmolytic for the gastrointestinal tract". The Journal of International Medical Research 27 (5): 207–22. 1999. doi:10.1177/030006059902700501. PMID 10689627. 
  4. "Otilonium bromide inhibits muscle contractions via L-type calcium channels in the rat colon". Neurogastroenterology and Motility 16 (2): 175–83. April 2004. doi:10.1111/j.1365-2982.2004.00518.x. PMID 15086871. 
  5. "T-type Ca(2+) channel modulation by otilonium bromide". American Journal of Physiology. Gastrointestinal and Liver Physiology 298 (5): G706-13. May 2010. doi:10.1152/ajpgi.00437.2009. PMID 20203058. 
  6. "Oral bioavailability and enterohepatic recirculation of otilonium bromide in rats". Archives of Pharmacal Research 31 (1): 117–24. January 2008. doi:10.1007/s12272-008-1129-2. PMID 18277617.