Tolnaftate

Chemical compound
  • D01AE18 (WHO)
Legal statusLegal status
  • In general: Over-the-counter (OTC)
Identifiers
  • O-2-Naphthyl methyl(3-methylphenyl)thiocarbamate
CAS Number
  • 2398-96-1 checkY
PubChem CID
  • 5510
DrugBank
  • DB00525 checkY
ChemSpider
  • 5309 checkY
UNII
  • 06KB629TKV
KEGG
  • D00381 checkY
ChEBI
  • CHEBI:9620 ☒N
ChEMBL
  • ChEMBL83668 checkY
CompTox Dashboard (EPA)
  • DTXSID3042477 Edit this at Wikidata
ECHA InfoCard100.017.516 Edit this at WikidataChemical and physical dataFormulaC19H17NOSMolar mass307.41 g·mol−13D model (JSmol)
  • Interactive image
Melting point110 to 111.5 °C (230.0 to 232.7 °F)
  • S=C(Oc2ccc1c(cccc1)c2)N(c3cc(ccc3)C)C
InChI
  • InChI=1S/C19H17NOS/c1-14-6-5-9-17(12-14)20(2)19(22)21-18-11-10-15-7-3-4-8-16(15)13-18/h3-13H,1-2H3 checkY
  • Key:FUSNMLFNXJSCDI-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Tolnaftate (INN)[1] is a synthetic thiocarbamate used as an anti-fungal agent that may be sold without medical prescription in most jurisdictions. It is supplied as a cream, powder, spray, liquid, and liquid aerosol.[2] Tolnaftate is used to treat fungal conditions such as jock itch, athlete's foot and ringworm.[2]

Mechanism

Although the exact mechanism of action is not entirely known, it is believed to inhibit squalene epoxidase,[3] an important enzyme in the biosynthetic pathway of ergosterol (a key component of the fungal cell membrane) in a similar way to terbinafine.[4]

Uses

Tolnaftate has been found to be generally slightly less effective than azoles when used to treat tinea pedis (athlete's foot). It is, however, useful when dealing with ringworm, especially when passed from pets to humans.[5]

Side effects

Side effects that may occur include:[6]

Less severe side effects include:[6]

  • dry skin
  • mild skin irritation, burning, or itching at the affected area

See also

References

  1. ^ a b "International Non-Proprietary Names for Pharmaceutical Preparations. Recommended International Non-Proprietary names (Rec. I.N.N.): List 6" (PDF). World Health Organization. Retrieved 12 November 2016.
  2. ^ a b "Tolnaftate". MedlinePlus,gov.
  3. ^ Ryder NS, Frank I, Dupont MC (May 1986). "Ergosterol biosynthesis inhibition by the thiocarbamate antifungal agents tolnaftate and tolciclate". Antimicrob. Agents Chemother. 29 (5): 858–60. doi:10.1128/aac.29.5.858. PMC 284167. PMID 3524433.
  4. ^ "antifung". Archived from the original on 2008-06-17. Retrieved 2008-07-09.
  5. ^ Crawford F, Hart R, Bell-Syer S, Torgerson D, Young P, Russell I. Topical treatments for fungal infections of the skin and nails of the foot (Cochrane Review). In: The Cochrane Library, Issue 1, 2003. Oxford: Update Software.
  6. ^ a b "Tolnaftate skin cream, gel, solution, or spray". Cleveland Clinic.

External links

  • Medline's entry for tolnaftate
  • v
  • t
  • e
Wall/
membrane
Ergosterol
inhibitors
Azoles (lanosterol 14α-
demethylase inhibitors)
Imidazoles
Triazoles
Thiazoles
Polyene antimycotics
(ergosterol binding)
Squalene monooxygenase
inhibitors
Allylamines
Benzylamines
Others
β-glucan synthase
inhibitors
Intracellular
Pyrimidine analogues/
thymidylate synthase inhibitors
Mitotic inhibitors
Aminoacyl tRNA synthetase inhibitors
Others
  • v
  • t
  • e
CARTooltip Constitutive androstane receptor
PXRTooltip Pregnane X receptor
See also
Receptor/signaling modulators