Description
Fluconazole is a triazole antifungal compound that inhibits fungal 14-α demethylase. Fluconazole is especially active against Candida and Cryptococcus.
Product Unit Size | Cost | Quantity | Stock |
---|
Fluconazole is a triazole antifungal compound that inhibits fungal 14-α demethylase. Fluconazole is especially active against Candida and Cryptococcus.
Cas No. | 86386-73-4 |
---|---|
Purity | ≥98% |
Formula | C13H12F2N6O |
Formula Wt. | 306.27 |
Chemical Name | α-(2,4-Difluorophenyl)-α-(1H-1,2,4-triazol-1- ylmethyl)-1H-1,2,4-triazole-1-ethanol |
IUPAC Name | 2-(2,4-difluorophenyl)-1,3-bis(1,2,4-triazol-1-yl)propan-2-ol |
Synonym | Biozolene, Diflucan, Elazor, Triflucan |
Melting Point | 138-140°C |
Solubility | Slightly soluble in water 1mg/mL. Soluble in ethanol (61mg/mL), ethyl acetate and methanol. DMSO to 100 mM. |
Appearance | White to off white powder |
Store Temp | Ambient |
---|---|
Ship Temp | Ambient |
MSDS | |
---|---|
Info Sheet |
Cuenca-Estrella M. Antifungal agents in the treatment of systemic infections: Relevance of mechanism of action, activity profile and resistances. Rev Esp Quimioter. 2010 Dec;23(4):169-76. PMID: 21191554.
Mansfield BE, Oltean HN, Oliver BG, et al. Azole drugs are imported by facilitated diffusion in Candida albicans and other pathogenic fungi. PLoS Pathog. 2010 Sep 30;6(9):e1001126. PMID: 20941354.
Matsumoto Y, Miyazaki S, Fukunaga DH, et al. Quantitative evaluation of cryptococcal pathogenesis and antifungal drugs using a silkworm infection model with Cryptococcus neoformans. J Appl Microbiol. 2012 Jan;112(1):138-146. PMID: 22040451.
Endogenous quaternary ammonium, required for fa...
MEK1/2 and Raf inhibitor.
Expectorant.
Pyridine; PDE3 inhibitor.
Endogenous bombesin-like peptide, involved in f...
Peptide deformylase, MMP meprin A, aminopeptida...
α1-Adrenergic antagonist.
Alpha blocker and vasoactive agent.
p110δ PI3K inhibitor.
Endogenous glycoprotein; lactoferrin agonist.
GSK-3 inhibitor.
Calpain I/II inhibitor.
Diterpene found in Anisomeles.
Ca2+ ATPase and ATP-sensitive K+ channel activa...
Bcl-2, Bcl-xl, sialyl transferase inhibitor.
Intermediate in the synthesis of purine analogs...
Nucleoside (adenosine) analog; DNA chain termin...
Benzothiazole; TRPC5 agonist, PTR1 inhibitor, v...
p110β PI3K inhibitor.
NO donor.