Dequalinium

Source: Wikipedia, the free encyclopedia.
Dequalinium
intravaginal
ATC code
Legal status
Legal status
Identifiers
  • 1,1'-decane-1,10-diylbis(4-amino-2-methylquinolinium) decyl]-2-methyl-4-quinolin-1-iumamine dichloride
JSmol)
  • c12ccccc1c(cc([n+]2CCCCCCCCCC[n+]4c3ccccc3c(N)cc4C)C)N
  • InChI=1S/C30H38N4/c1-23-21-27(31)25-15-9-11-17-29(25)33(23)19-13-7-5-3-4-6-8-14-20-34-24(2)22-28(32)26-16-10-12-18-30(26)34/h9-12,15-18,21-22,31-32H,3-8,13-14,19-20H2,1-2H3/p+2
  • Key:PCSWXVJAIHCTMO-UHFFFAOYSA-P

Dequalinium is a quaternary ammonium cation and bolaamphiphile commonly available as the dichloride salt. It is useful as an antiseptic and disinfectant. The bromide, iodide, acetate, and undecenoate salts are known as well. Dequalinium chloride is the active ingredient of several medications.

The dequalinium dication is symmetrical, containing two quaternary quinolinium units linked by an N-decylene chain.

Medical uses

Dequalinium chloride 0.25 mg is available as an

over-the-counter throat lozenge under brand names such as Dequadin and SP Troche. Mouthwash and buccal sprays at 0.5 % concentration are also available.[3][unreliable medical source?] In this form is it used to treat minor infections of the mouth and throat. It can help with tonsillitis but is not effective in cases of streptococci infections.[4]

The product is also available as a 10 mg prescription

bacterial Vaginosis and aerobic vaginitis). Brand names include Fluomizin and Vablys.[3]

In Austria, dequalinium chloride is combined with bacitracin and diphenylpyraline in Eucillin "B", an antibiotic cream. This cream is the first dequalinium-containing product to enter Austria in 1967.[3]

Spectrum of activity

Dequalinium salts have broad bactericidal and fungicidal activity.

bacteriostat.[citation needed
]

Dequalinium salts may have antimalarial activities.[6]

Adverse effects

Dequalinium may cause

intertriginous skin areas under occlusive conditions".[6]

History

Dequalinium was first described by M Babbs and colleagues in 1956, as the first agent of the bisquaternary ammonium chemical class.[7]

References

  1. ^ "Health product highlights 2021: Annexes of products approved in 2021". Health Canada. 3 August 2022. Retrieved 25 March 2024.
  2. ^ "Fluomizin Summary of Product Characteristics (SmPC)". (emc). 12 October 2022. Retrieved 14 April 2024.
  3. ^ a b c "Dequalinium". DrugBank Online.
  4. PMID 856702
    .
  5. .
  6. ^ .
  7. .

Further reading

External links