Tolnaftate

Tolnaftate
Clinical data
Trade names	Tinactin
Other names	2-Naphthyl N-methyl-N-(3-tolyl)thionocarbamate
AHFS/Drugs.com	Monograph
MedlinePlus	a682617
ATC code	D01AE18 (WHO) ;
Legal status
Legal status	In general: Over-the-counter (OTC);
Identifiers
	IUPAC name O-2-Naphthyl methyl(3-methylphenyl)thiocarbamate;
CAS Number	2398-96-1 ;
PubChem CID	5510;
DrugBank	DB00525 ;
ChemSpider	5309 ;
UNII	06KB629TKV;
KEGG	D00381 ;
ChEBI	CHEBI:9620 ;
ChEMBL	ChEMBL83668 ;
CompTox Dashboard (EPA)	DTXSID3042477 ;
ECHA InfoCard	100.017.516
Chemical and physical data
Formula	C19H17NOS
Molar mass	307.41 g·mol−1
3D model (JSmol)	Interactive image;
Melting point	110 to 111.5 °C (230.0 to 232.7 °F)
	SMILES 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 ; Key:FUSNMLFNXJSCDI-UHFFFAOYSA-N ;
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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]

allergic reactions like:
- skin rash
- itching or hives
- swelling of the face, lips, or tongue
inflammation, redness, or pain at the affected area

Less severe side effects include:^[6]

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

References

^ ^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.
^ ^a ^b "Tolnaftate". MedlinePlus,gov.
^ 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.
^ "antifung". Archived from the original on 2008-06-17. Retrieved 2008-07-09.
^ 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.
^ ^a ^b "Tolnaftate skin cream, gel, solution, or spray". Cleveland Clinic.

External links

[INN-1] "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.

[:1-2] "Tolnaftate". MedlinePlus,gov.

[pmid3524433-3] 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.

[urlantifung-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.

[:0-6] "Tolnaftate skin cream, gel, solution, or spray". Cleveland Clinic.

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