Date published: 2026-2-7

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Tolnaftate (CAS 2398-96-1)

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Alternate Names:
Methyl-(3-methylphenyl)carbamothioic acid O-2-naphthyl ester
CAS Number:
2398-96-1
Purity:
98%
Molecular Weight:
307.41
Molecular Formula:
C19H17NOS
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Tolnaftate, a synthetic thiocarbamate compound, has been extensively researched in scientific circles, particularly in the field of antifungal agents and dermatology. Researchers have delved into its mechanisms of action and its efficacy against various fungal pathogens, shedding light on its potential applications in combating fungal infections. One of the key mechanisms underlying tolnaftate′s antifungal activity is its inhibition of fungal squalene epoxidase, an enzyme crucial in the ergosterol biosynthesis pathway. Ergosterol is vital for fungal cell membranes, and its depletion disrupts membrane integrity and function, ultimately leading to fungal cell death. Studies have employed biochemical and molecular techniques to explain the interaction between tolnaftate and squalene epoxidase, providing insights into the structural basis of enzyme inhibition and the development of resistance mechanisms. Moreover, tolnaftate has shown broad-spectrum antifungal activity against various dermatophyte species, which commonly cause skin infections. Research efforts have focused on optimizing formulations and delivery systems to enhance the topical efficacy of tolnaftate and improve outcomes.


Tolnaftate (CAS 2398-96-1) References

  1. Evaluation of the effectiveness of griseofulvin, tolnaftate, and placebo in the topical therapy of superficial dermatophytoses.  |  Zarowny, DP., et al. 1975. J Invest Dermatol. 64: 268-72. PMID: 1090684
  2. Assay of tolnaftate in human skin samples after in vitro penetration studies using high performance liquid chromatography.  |  Kezutyte, T., et al. 2010. Acta Pol Pharm. 67: 327-34. PMID: 20635527
  3. The solid-state conformation of the topical antifungal agent O-naphthalen-2-yl N-methyl-N-(3-methylphenyl)carbamothioate.  |  Ho, DM. and Zdilla, MJ. 2018. Acta Crystallogr C Struct Chem. 74: 1495-1501. PMID: 30398206
  4. Tolnaftate inhibits ergosterol production and impacts cell viability of Leishmania sp.  |  Yamamoto, ES., et al. 2020. Bioorg Chem. 102: 104056. PMID: 32653607
  5. The mode of antifungal action of tolnaftate.  |  Barrett-Bee, KJ., et al. 1986. J Med Vet Mycol. 24: 155-60. PMID: 3522841
  6. Ergosterol biosynthesis inhibition by the thiocarbamate antifungal agents tolnaftate and tolciclate.  |  Ryder, NS., et al. 1986. Antimicrob Agents Chemother. 29: 858-60. PMID: 3524433
  7. Advances of liposomal mediated nanocarriers for the treatment of dermatophyte infections.  |  Ayatollahi Mousavi, SA., et al. 2023. Heliyon. 9: e18960. PMID: 37583758
  8. Flexosomes as a promising nanoplatform for enhancing tolnaftate ocular delivery: Formulation, in vitro characterization, statistical optimization, ex vivo and microbial in vivo studies.  |  Aziz, D., et al. 2023. Int J Pharm. 646: 123471. PMID: 37793467
  9. Toxicologic and pharmacologic properties of tolnaftate, an antitrichophyton agent.  |  Hashimoto, Y., et al. 1966. Toxicol Appl Pharmacol. 8: 380-5. PMID: 5961557
  10. Inhibition of aflatoxin biosynthesis by tolnaftate.  |  Khan, SN., et al. 1978. Appl Environ Microbiol. 36: 270-3. PMID: 697362

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Tolnaftate, 1 g

sc-237124
1 g
$64.00