Description
Tioconazole is an imidazole antifungal and antibacterial compound that damages cell membranes. Tioconazole is most active against fungi, molds, and gram positive bacteria.
| Product Unit Size | Cost | Quantity | Stock |
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Tioconazole is an imidazole antifungal and antibacterial compound that damages cell membranes. Tioconazole is most active against fungi, molds, and gram positive bacteria.
| Cas No. | 65899-73-2 |
|---|---|
| Purity | ≥98% |
| Formula | C16H13Cl3N2OS |
| Formula Wt. | 387.71 |
| Chemical Name | 1-[2-[(2-Chloro-3-thienyl)methoxy]-2-(2,4- dichlorophenyl)ethyl]-1H-imidazole |
| IUPAC Name | 1-[2-[(2-chlorothiophen-3-yl)methoxy]-2-(2, 4-dichlorophenyl)ethyl]imidazole |
| Synonym | Vagistat, Fungibacid, Trosyd, Zoniden |
| Melting Point | 168-170°C |
| Solubility | Moderately soluble in chloroform, ethanol, methanol or ethyl acetate. |
| Appearance | White or almost white crystalline powder |
| Store Temp | Ambient |
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| Ship Temp | Ambient |
| MSDS | |
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| Info Sheet |
Jones RN, Bale MJ, Hoban D, et al. In vitro antimicrobial activity of tioconazole and its concentrations in vaginal fluids following topical (vagistat-1 6.5%) application. Diagn Microbiol Infect Dis. 1993 Jul;17(1):45-51. PMID: 8359005.
Odds FC, Cheesman SL, Abbott AB. Suppression of ATP in Candida albicans by imidazole and derivative antifungal agents. Sabouraudia. 1985 Dec;23(6):415-24. PMID: 3913012.
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Potential PKD binding agent.
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H+/K+ ATPase inhibitor.
Synthesis impurity
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MEK inhibitor.
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Inhibitor of FAK and ALK.
CRM1/XPO1 inhibitor.