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Synonyms: UK-49858

| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 50 mg | $36 | In Stock | In Stock | |
| 100 mg | $48 | In Stock | In Stock | |
| 200 mg | $59 | In Stock | In Stock | |
| 500 mg | $72 | In Stock | In Stock | |
| 1 mL x 10 mM (in DMSO) | $30 | In Stock | In Stock |
| Description | Fluconazole (UK-49858) belongs to the triazole class of antifungal agents and is a CYP51 inhibitor (IC99 = 0.20–0.39 μg/mL against Candida albicans), possessing broad-spectrum antifungal activity, good oral absorption, and cell permeability. This compound is used for the treatment of various invasive fungal infections. |
| In vitro | Methods: The in vitro antifungal activity of Fluconazole against clinically isolated Candida species was determined by CLSI M27-E4 broth microdilution method, with incubation for 24-48 hours. Results: The MIC90 of Fluconazole against Candida albicans was 2 μg/mL, with a susceptibility rate of 92%; against Candida glabrata, the MIC90 was 16 μg/mL, with 98% showing dose-dependent susceptibility. The wild-type proportion of Fluconazole for recurrent VVC strains was significantly lower than other types (67% vs 77%).[1] Methods: Broth microdilution method was used to determine the in vitro activity of Fluconazole against Candida. YPD medium was used, with Fluconazole concentrations ranging from 0-128 μg/mL (two-fold dilutions), inoculation of 2×10^5 CFU/mL Candida, and incubation at 30°C for 24 hours before MIC reading. Results: Fluconazole showed good inhibitory effects against susceptible strains, but MIC values were significantly elevated against resistant strains.[2] |
| In vivo | Methods: A Galleria mellonella larval systemic infection model with Candida albicans was established. Fluconazole (20 μg/mL, 10 μL per larva, dissolved in DMSO) was administered by single injection 1.5-2 hours post-infection. Results: Fluconazole monotherapy significantly prolonged the median survival time of infected larvae (9.33 days vs 2.33 days) and reduced fungal burden.[2] |
| Synonyms | UK-49858 |
| Molecular Weight | 306.27 |
| Formula | C13H12F2N6O |
| Cas No. | 86386-73-4 |
| Smiles | FC1=CC=C(C(F)=C1)C(O)(CN2N=CN=C2)CN3N=CN=C3 |
| Relative Density. | 1.49 g/cm3 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. | ||||||||||||||||||||||||||||||||||||||||
| Solubility Information | Ethanol: 30.6 mg/mL (99.91 mM), Sonication is recommended. DMSO: 260 mg/mL (848.92 mM), Sonication is recommended. | ||||||||||||||||||||||||||||||||||||||||
| In Vivo Formulation | 10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (6.53 mM), Sonication is recommended. Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions. | ||||||||||||||||||||||||||||||||||||||||
Solution Preparation Table | |||||||||||||||||||||||||||||||||||||||||
Ethanol/DMSO
DMSO
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density. | |||||||||||||||||||||||||||||||||||||||||
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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