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Xylometazoline information


Xylometazoline
Clinical data
Pronunciation/ˌzlˌmɛtəˈzln/
ZY-lo-MET-ə-ZOH-leen
Trade namesOtrivin, Otrivine, others
AHFS/Drugs.comMonograph
MedlinePlusa608026
License data
  • US DailyMed: Xylometazoline
Pregnancy
category
  • C
Dependence
liability
Moderate[1]
Routes of
administration
intranasal (spray or drops)
Drug classα1 and α2 Adrenergic receptor agonist,
Decongestant
ATC code
  • R01AA07 (WHO) S01GA03 (WHO)
Legal status
Legal status
  • In general: Over-the-counter (OTC)
Pharmacokinetic data
Elimination half-life>10 seconds
ExcretionUrinary
Identifiers
IUPAC name
  • 2-[(4-tert-butyl-2,6-dimethylphenyl)methyl]-
    4,5-dihydro-1H-imidazole
CAS Number
  • 526-36-3 ☒N
PubChem CID
  • 5709
IUPHAR/BPS
  • 517
DrugBank
  • DB06694 checkY
ChemSpider
  • 5507 checkY
UNII
  • WPY40FTH8K
KEGG
  • D08684 checkY
ChEMBL
  • ChEMBL312448 checkY
CompTox Dashboard (EPA)
  • DTXSID8046957 Edit this at Wikidata
ECHA InfoCard100.007.629 Edit this at Wikidata
Chemical and physical data
FormulaC16H24N2
Molar mass244.382 g·mol−1
3D model (JSmol)
  • Interactive image
SMILES
  • N\1=C(\NCC/1)Cc2c(cc(cc2C)C(C)(C)C)C
InChI
  • InChI=1S/C16H24N2/c1-11-8-13(16(3,4)5)9-12(2)14(11)10-15-17-6-7-18-15/h8-9H,6-7,10H2,1-5H3,(H,17,18) checkY
  • Key:HUCJFAOMUPXHDK-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Xylometazoline, also spelled xylomethazoline, is a medication used to reduce symptoms of nasal congestion, allergic rhinitis, and sinusitis.[2] Use is not recommended for more than seven days.[3] Use is also not recommended in those less than three months of age and some say not less than 6 years of age.[3][4] It is used directly in the nose as a spray or drops.[3]

Side effects include trouble sleeping, irritation of the nose, nausea, nosebleed (3%), period pain (10%) and headache (3%).[5][2][3] Long term use (> 10 days) is not recommended due to a rhinitis medicamentosa when stopped.[5][6] Use is not recommended during pregnancy.[2] Xylometazoline is in the decongestant and alpha-adrenergic agonist families of medication.[6][7]

One study classified it with selectivity ratios in alpha 2 adrenergic receptors of 151 for a2A vs a2B, 4.5 a2A vs a2C, and 33.9 a2B vs a2C.  Making it a highly selective a2A agonist.[8]

Xylometazoline was patented in 1956 and came into medical use in 1959.[9][10] It is on the World Health Organization's List of Essential Medicines.[4][11] Xylometazoline is available as a generic medication.[3]

  1. ^ {{Fulga, Ana, Andrei Zenovia, Doriana Cristea Ene, Constantin Stan, Dorel Firescu, and Iuliu Fulga. 2021. “Addiction to Nasal Decongestants Based on Α-Adrenoceptor Agonists Case Series and Literature Review: Array”. EuroEconomica 40 (2). https://dj.univ-danubius.ro/index.php/EE/article/view/1455}}
  2. ^ a b c "Otrivine Adult Measured Dose Sinusitis Spray - Summary of Product Characteristics (SPC) - (eMC)". www.medicines.org.uk. 13 April 2016. Archived from the original on 29 December 2016. Retrieved 28 December 2016.
  3. ^ a b c d e British national formulary : BNF 69 (69 ed.). British Medical Association. 2015. p. 786. ISBN 978-0-85711-156-2.
  4. ^ a b World Health Organization (2019). World Health Organization model list of essential medicines: 21st list 2019. Geneva: World Health Organization. hdl:10665/325771. WHO/MVP/EMP/IAU/2019.06. License: CC BY-NC-SA 3.0 IGO.
  5. ^ a b Eccles R, Martensson K, Chen SC (April 2010). "Effects of intranasal xylometazoline, alone or in combination with ipratropium, in patients with common cold". Current Medical Research and Opinion. 26 (4): 889–899. doi:10.1185/03007991003648015. PMID 20151787. S2CID 34728458.
  6. ^ a b Graf P (1997). "Rhinitis medicamentosa: aspects of pathophysiology and treatment". Allergy. 52 (40 Suppl): 28–34. doi:10.1111/j.1398-9995.1997.tb04881.x. PMID 9353558. S2CID 72326981.
  7. ^ "Xylometazoline nasal medical facts from Drugs.com". www.drugs.com. Archived from the original on 29 December 2016. Retrieved 28 December 2016.
  8. ^ Proudman RG, Akinaga J, Baker JG (October 2022). "The signaling and selectivity of α-adrenoceptor agonists for the human α2A, α2B and α2C-adrenoceptors and comparison with human α1 and β-adrenoceptors". Pharmacology Research & Perspectives. 10 (5): e01003. doi:10.1002/prp2.1003. PMC 9471048. PMID 36101495.
  9. ^ Fischer J, Ganellin CR (2006). Analogue-based Drug Discovery. John Wiley & Sons. p. 552. ISBN 978-3-527-60749-5. Archived from the original on 29 December 2016.
  10. ^ US patent 2868802A, Hüni, Albrecht, "2-(γ-TERT-BUTYL-O,O'-DIMETHYL-PHENYL-METHYL)-IMIDAZOLINE AND SALTS", issued 1959-01-13, assigned to Ciba Pharmaceutical Products Inc., Summit, N. J. 
  11. ^ World Health Organization (2021). World Health Organization model list of essential medicines: 22nd list (2021). Geneva: World Health Organization. hdl:10665/345533. WHO/MHP/HPS/EML/2021.02.

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