Nifuratel

Chemical compound
  • G01AX05 (WHO)
Identifiers
  • 5-[(Methylthio)methyl]-3-{[(1E)-(5-nitro-2-furyl)methylene]amino}-1,3-oxazolidin-2-one
CAS Number
  • 4936-47-4 checkY
PubChem CID
  • 6433427
ChemSpider
  • 4938579
UNII
  • U60U6P08SP
KEGG
  • D01050 checkY
ECHA InfoCard100.023.251 Edit this at WikidataChemical and physical dataFormulaC10H11N3O5SMolar mass285.27 g·mol−13D model (JSmol)
  • Interactive image
  • CSCC1CN(C(=O)O1)/N=C/C2=CC=C(O2)[N+](=O)[O-]
InChI
  • InChI=1S/C10H11N3O5S/c1-19-6-8-5-12(10(14)18-8)11-4-7-2-3-9(17-7)13(15)16/h2-4,8H,5-6H2,1H3/b11-4+
  • Key:SRQKTCXJCCHINN-NYYWCZLTSA-N
  (verify)

Nifuratel (brand name Macmiror, or — in combination with nystatin, — Macmiror Complex) is a drug used in gynecology. It is a local antiprotozoal and antifungal agent that may also be given orally. Nifuratel is not approved for use in the United States.

Nifuratel appears to have a broad antibacterial spectrum of action and is effective against Chlamydia trachomatis and Mycoplasma spp. as well as fungal infections from Candida spp.[1]

Taken orally, or as a vaginal pessary, it is used in the treatment of a wide range of infections of the genito-urinary tract, especially if there is no accurate diagnosis available. For example, it may be used in the treatment of women exhibiting vaginal discharge where there is uncertainty as to whether the cause is Trichomonas vaginalis or Candida strains such as Candida albicans.

Side effects appear to be minimal or non-existent and it has a safe toxicological profile.[2]

References

  1. ^ Grüneberg RN, Leakey A (October 1976). "Treatment of candidal urinary tract infection with nifuratel". British Medical Journal. 2 (6041): 908–10. doi:10.1136/bmj.2.6041.908. PMC 1688487. PMID 974657.
  2. ^ Mendling W, Mailland F (2002). "Microbiological and pharmaco-toxicological profile of nifuratel and its favourable risk/benefit ratio for the treatment of vulvo-vaginal infections. A review". Arzneimittel-Forschung. 52 (1): 8–13. doi:10.1055/s-0031-1299849. PMID 11838277.
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