1-Docosanol

1-Docosanol
Names
Preferred IUPAC name
Docosan-1-ol[1]
Other names
Behenic alcohol[1]

Behenyl alcohol[1]
Cachalot BE-22
1-Docosanol[2]
n-Docosanol[2]
Docosyl alcohol[1]
Emery 3304[2]

Loxiol VPG 1451
Identifiers
CAS Number
3D model (JSmol)
Beilstein Reference
 1770470
ChEBI
ChEMBL
ChemSpider
DrugBank
ECHA InfoCard 100.010.498
EC Number
  • 211-546-6
KEGG
MeSH docosanol
PubChem CID
RTECS number
  • JR1315000
UNII
InChI
  • InChI=1S/C22H46O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23/h23H,2-22H2,1H3 Y
    Key: NOPFSRXAKWQILS-UHFFFAOYSA-N Y
  • InChI=1/C22H46O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23/h23H,2-22H2,1H3
    Key: NOPFSRXAKWQILS-UHFFFAOYAB
SMILES
  • CCCCCCCCCCCCCCCCCCCCCCO
Properties
Chemical formula
 C22H46O
Molar mass 326.609 g·mol−1
Melting point 70 °C; 158 °F; 343 K
Boiling point 180 °C; 356 °F; 453 K at 29 Pa
log P 10.009
Pharmacology
D06BB11 (WHO)
Topical
Legal status
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YN ?)
Infobox references

1-Docosanol, also known as behenyl alcohol, is a saturated fatty alcohol containing 22 carbon atoms, used traditionally as an emollient, emulsifier, and thickener in cosmetics.[6]

In July 2000, docosanol was approved for medical use in the United States as an antiviral agent for reducing the duration of cold sores.[3][4][7] It is an over-the-counter medication (OTC). It is sold under the brand name Abreva among others.[3][5][8][9]

Side effects

One of the most common side effects that has been reported from docosanol is headache. Headaches caused by the medication tend to be mild and can occur in any region of the head.[10] In clinical trials, headache occurred in 10.4% of people treated with docosanol cream and 10.7% of people treated with placebo.[8]

The most serious side effects, although rare, are allergic reactions. Some of the patients experienced the symptoms of allergic reactions, including difficulty breathing, confusion, angioedema (facial swelling), fainting, dizziness, hives or chest pain.[10]

Other side effects may include: acne, burning, dryness, itching, rash, redness, acute diarrhea, soreness, swelling.[11]

Mechanism of action

Docosanol is thought to act by inhibiting the fusion of the human host cell with the viral envelope of the herpes virus, thus preventing its replication.[8][12]

History

The drug was approved as a cream for oral herpes after clinical trials by the FDA in July 2000.[4][13] It was shown to shorten the healing by 17.5 hours on average (95% confidence interval: 2 to 22 hours) in a placebo-controlled trial.[14] Another trial showed no effect when treating the infected backs of guinea pigs.[15]

Two experiments with n-docosanol cream failed to show statistically significant differences by any parameter between n-docosanol cream and vehicle control–treated sites or between n-docosanol and untreated infection sites.[15]

Society and culture

Controversy

In March 2007, it was the subject of a US nationwide class-action suit against Avanir and GlaxoSmithKline as the claim that it cut recovery times in half was found to have been misleading in a California court, but the case was eventually settled and the "cuts healing time in half" claim had not been used in product advertising for some years.[16]

References
  1. "Docosan-1-ol (CHEBI:31000)". Chemical Entities of Biological Interest (ChEBI). UK: European Bioinformatics Institute.
  2. Chemical Book: 1-Docosanol
  3. "Abreva- docosanol cream". DailyMed. 18 April 2022. Retrieved 14 October 2022.
  4. "Drug Approval Package: Abreva (Docosanol) NDA #20-941". U.S. Food and Drug Administration (FDA). 21 August 2001. Retrieved 13 October 2022.
  5. "List of nationally authorised medicinal products" (PDF). ema.europa.eu. European Medicines Agency. 2 December 2021. Archived (PDF) from the original on 15 October 2022. Retrieved 23 October 2022.
  6. "CosIng: Behenyl alcohol". European Commission. Retrieved 14 March 2021.
  7. Katz DH, Marcelletti JF, Khalil MH, Pope LE, Katz LR (December 1991). "Antiviral activity of 1-docosanol, an inhibitor of lipid-enveloped viruses including herpes simplex". Proc. Natl. Acad. Sci. U.S.A. 88 (23): 10825–10829. Bibcode:1991PNAS...8810825K. doi:10.1073/pnas.88.23.10825. PMC 53024. PMID 1660151.
  8. Haberfeld H, ed. (2020). Austria-Codex (in German). Vienna: Österreichischer Apothekerverlag. Erazaban Creme.
  9. "mediLexicon: Docosanol". Archived from the original on 10 March 2013. Retrieved 2 September 2008.
  10. "Abreva Side Effects". Livestrong.com. Retrieved 20 May 2010.
  11. "Side Effects". Drugs.com. Retrieved 20 May 2010.
  12. Docosanol Monograph. Accessed 14 March 2021.
  13. "Drug Name: Abreva (docosanol) – approval". centerwatch.com. July 2000. Archived from the original on 6 October 2008. Retrieved 17 October 2007.
  14. Sacks, SL; Thisted, RA; Jones, TM; Barbarash, RA; Mikolich, DJ; Ruoff, GE; Jorizzo, JL; Gunnill, LB; et al. (2001). "Clinical efficacy of topical docosanol 10% cream for herpes simplex labialis: A multicenter, randomized, placebo-controlled trial". J Am Acad Dermatol. 45 (2): 222–230. doi:10.1067/mjd.2001.116215. PMID 11464183.
  15. McKeough, MB; Spruance, SL (2001). "Comparison of new topical treatments for herpes labialis: Efficacy of penciclovir cream, acyclovir cream, and n-docosanol cream against experimental cutaneous herpes simplex virus type 1 infection". Archives of Dermatology. 137 (9): 1153–1158. doi:10.1001/archderm.137.9.1153. PMID 11559210.
  16. "California Court Upholds Settlement Of Class Action Over Cold Sore Medicationl". BNA Inc. July 2000. Archived from the original on 5 February 2008. Retrieved 17 October 2007.
  • "Docosanol". Drug Information Portal. U.S. National Library of Medicine.
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