(±)-Voriconazole
Based on 1 Customer Validation
(±)-Voriconazole ((±)-UK-109496) is a relative configuration of Voriconazole (HY-76200). Voriconazole is an antifungal agent.
For research use only. We do not sell to patients.
- Purity: 99.06%
- CAS No.: 188416-29-7
- Formula: C16H14F3N5O
- Molecular Weight:349.31
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Storage:Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 6 months , -20°C, 1 month
Biological Activity
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| A549 | IC50 |
>30 μM
Compound: VOR
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Cytotoxicity against human A549 cells assessed as reduction in cell viability measured after 96 hrs by MTT assay
Cytotoxicity against human A549 cells assessed as reduction in cell viability measured after 96 hrs by MTT assay
|
[PMID: 34388384] |
| CHO | IC50 |
>40 μM
Compound: 3
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Inhibition of human ERG expressed in CHO cells by whole-cell patch clamp assay
Inhibition of human ERG expressed in CHO cells by whole-cell patch clamp assay
|
[PMID: 24564525] |
| CHO | IC50 |
414.2 μM
Compound: voriconazole
|
Inhibition of Cav1.2 current measured using QPatch automatic path clamp system in CHO cells expressing Cav1.2, beta-2 and alpha-2/delta-1 subunits
Inhibition of Cav1.2 current measured using QPatch automatic path clamp system in CHO cells expressing Cav1.2, beta-2 and alpha-2/delta-1 subunits
|
[PMID: 23812503] |
| Hepatocyte | IC50 |
13 μM
Compound: Voriconazole
|
Inhibition of CYP3A4 in human hepatocytes using testosterone as substrate by HPLC/MS/MS method
Inhibition of CYP3A4 in human hepatocytes using testosterone as substrate by HPLC/MS/MS method
|
[PMID: 24948565] |
| MCF7 | IC50 |
>30 μM
Compound: VOR
|
Cytotoxicity against human MCF7 cells assessed as reduction in cell viability measured after 96 hrs by MTT assay
Cytotoxicity against human MCF7 cells assessed as reduction in cell viability measured after 96 hrs by MTT assay
|
[PMID: 34388384] |
| MRC5 | IC50 |
40 μg/mL
Compound: VOR
|
Cytotoxicity against human MRC5 cells after 48 hrs by MTT assay
Cytotoxicity against human MRC5 cells after 48 hrs by MTT assay
|
[PMID: 26867487] |
| MRC5 | IC50 |
40 μg/mL
Compound: Voriconazole
|
Cytotoxicity against human MRC5 cells after 48 hrs by MTT assay
Cytotoxicity against human MRC5 cells after 48 hrs by MTT assay
|
[PMID: 26586600] |
| THLE-2 | IC50 |
>30 μM
Compound: VOR
|
Cytotoxicity against human THLE-2 cells assessed as reduction in cell viability measured after 96 hrs by MTT assay
Cytotoxicity against human THLE-2 cells assessed as reduction in cell viability measured after 96 hrs by MTT assay
|
[PMID: 34388384] |
Chemical Information
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CAS No. 188416-29-7
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Appearance Solid
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Molecular Weight 349.31
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Formula C16H14F3N5O
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Color White to off-white
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SMILES
O[C@@]([C@@H](C)C1=NC=NC=C1F)(CN2N=CN=C2)C(C(F)=C3)=CC=C3F
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Synonyms
(±)-UK-109496
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month
Solvent & Solubility
DMSO : 100 mg/mL (286.28 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Select the appropriate dissolution method based on your experimental animal and administration route.
- For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
- To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for In Vivo experiments, it is recommended to prepare freshly and use it on the same day.
- The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.
Please enter the basic information of animal experiments:
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-
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Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Please enter your animal formula composition:
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%DMSO +
Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
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%+
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+%Tween-80 + +
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%Saline +
The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).
Working solution concentration: 0.22 mg/mL
Method for preparing stock solution: mg drug dissolved in μL DMSO. Stock solution concentration: mg/mL.
1. Take μL DMSO stock solution;
2. Add μL .
μL , mix evenly;
3. Then add μL Tween 80, mix evenly;
4. Then add μL
Please ensure that the stock solution in the first step is dissolved to a clear state, and add co-solvents in sequence. You can use ultrasonic heating (ultrasonic cleaner, recommended frequency 20-40 kHz), vortexing, etc. to assist dissolution.
Purity & Documentation
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Data Sheet (276 KB)
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SDS (393 KB)
- English - EN (393 KB)
- Français - FR (393 KB)
- Deutsch - DE (393 KB)
- Norwegian - NO (393 KB)
- Español - ES (393 KB)
- Swedish - SV (393 KB)
- Italian - IT (393 KB)
- Korean - KR (393 KB)
- Portuguese - PT (393 KB)
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Handling Instructions (2659 KB)
References
Complete Stock Solution Preparation Table
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
| Optional Solvent | Concentration Solvent Mass | 1 mg | 5 mg | 10 mg | 25 mg |
|---|---|---|---|---|---|
| DMSO | 1 mM | 2.8628 mL | 14.3139 mL | 28.6279 mL | 71.5697 mL |
| 5 mM | 0.5726 mL | 2.8628 mL | 5.7256 mL | 14.3139 mL | |
| 10 mM | 0.2863 mL | 1.4314 mL | 2.8628 mL | 7.1570 mL | |
| 15 mM | 0.1909 mL | 0.9543 mL | 1.9085 mL | 4.7713 mL | |
| 20 mM | 0.1431 mL | 0.7157 mL | 1.4314 mL | 3.5785 mL | |
| 25 mM | 0.1145 mL | 0.5726 mL | 1.1451 mL | 2.8628 mL | |
| 30 mM | 0.0954 mL | 0.4771 mL | 0.9543 mL | 2.3857 mL | |
| 40 mM | 0.0716 mL | 0.3578 mL | 0.7157 mL | 1.7892 mL | |
| 50 mM | 0.0573 mL | 0.2863 mL | 0.5726 mL | 1.4314 mL | |
| 60 mM | 0.0477 mL | 0.2386 mL | 0.4771 mL | 1.1928 mL | |
| 80 mM | 0.0358 mL | 0.1789 mL | 0.3578 mL | 0.8946 mL | |
| 100 mM | 0.0286 mL | 0.1431 mL | 0.2863 mL | 0.7157 mL |