Date published: 2025-11-11

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Tioconazole (CAS 65899-73-2)

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Alternate Names:
Vagistat; Trosyd
Application:
Tioconazole is a cytochrome-P450 inhibitor
CAS Number:
65899-73-2
Purity:
98%
Molecular Weight:
387.71
Molecular Formula:
C16H13Cl3N2OS
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Tioconazole, identified by CAS number 65899-73-2, is a synthetic antifungal agent belonging to the imidazole class of compounds. It functions through a mechanism of action that involves the inhibition of fungal cytochrome P450 enzymes, primarily lanosterol 14α-demethylase. This enzyme is crucial in the biosynthetic pathway of ergosterol, a key component of the fungal cell membrane. By inhibiting this enzyme, tioconazole disrupts the production of ergosterol, leading to an increase in cellular permeability and ultimately causing cell lysis and death of the fungus. Tioconazole′s potent antifungal activity and specific target interaction make it a valuable tool in microbiological research, especially for studies focused on fungal biology and the mechanisms of antifungal resistance. Researchers utilize tioconazole to explore the dynamics of fungal population adaptations to environmental pressures and to understand the genetic and biochemical bases of resistance to imidazole compounds. Additionally, studies involving tioconazole help in mapping out the fungal sterol synthesis pathway, providing insights into potential new targets for antifungal therapy. This research contributes to a broader understanding of fungal diseases and aids in the development of strategies to manage fungal infections more effectively.


Tioconazole (CAS 65899-73-2) References

  1. In vitro antimicrobial activity of ethanol and water extracts of Cassia alata.  |  Somchit, MN., et al. 2003. J Ethnopharmacol. 84: 1-4. PMID: 12499068
  2. High affinity inhibition of Ca(2+)-dependent K+ channels by cytochrome P-450 inhibitors.  |  Alvarez, J., et al. 1992. J Biol Chem. 267: 11789-93. PMID: 1376313
  3. Activity of Fenticonazole, Tioconazole and Nystatin on New World Leishmania Species.  |  Yamamoto, ES., et al. 2018. Curr Top Med Chem. 18: 2338-2346. PMID: 30569856
  4. Design and Characterization of Chitosan Nanoformulations for the Delivery of Antifungal Agents.  |  Calvo, NL., et al. 2019. Int J Mol Sci. 20: PMID: 31357647
  5. Formulation of Tioconazole and Melaleuca alternifolia Essential Oil Pickering Emulsions for Onychomycosis Topical Treatment.  |  Vörös-Horváth, B., et al. 2020. Molecules. 25: PMID: 33256033
  6. Development and optimization of a new tioconazole vaginal mucoadhesive film using an experimental design strategy. Physicochemical and biological characterization.  |  Calvo, NL., et al. 2021. J Pharm Biomed Anal. 205: 114303. PMID: 34391134
  7. Characterization of the hydrochloride salt hemihydrate as a new salt of the antifungal agent tioconazole.  |  Moroni, AB., et al. 2023. Int J Pharm. 637: 122869. PMID: 36948477
  8. Microbiological and spectrophotometric methods for the determination of tioconazole: A comparative thermodynamic study.  |  Elmasry, MS., et al. 2023. Spectrochim Acta A Mol Biomol Spectrosc. 298: 122770. PMID: 37119638
  9. Preparation and characterization of new salts of tioconazole. Comparison of their dissolution performance.  |  Moroni, AB., et al. 2024. Int J Pharm. 652: 123855. PMID: 38280497

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Tioconazole, 1 g

sc-205864
1 g
$75.00

Tioconazole, 5 g

sc-205864A
5 g
$118.00