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Butibufen
Catalog No. T26926Cas No. 55837-18-8
Alias FF-106, FF106, FF 106, FF 105
Butibufen (FF-106) is an orally active non-steroidal anti-inflammatory compound, a potential cyclooxygenase inhibitor with analgesic and antipyretic activity, and inhibits urea synthesis.Butibufen has been used in the study of rheumatic diseases.
Butibufen
Purity: 99.29%
Catalog No. T26926Alias FF-106, FF106, FF 106, FF 105Cas No. 55837-18-8
Butibufen (FF-106) is an orally active non-steroidal anti-inflammatory compound, a potential cyclooxygenase inhibitor with analgesic and antipyretic activity, and inhibits urea synthesis.Butibufen has been used in the study of rheumatic diseases.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 1 mg | $35 | In Stock | |
| 5 mg | $76 | In Stock | |
| 10 mg | $109 | In Stock | |
| 25 mg | $179 | In Stock | |
| 50 mg | $267 | In Stock | |
| 100 mg | $396 | In Stock | |
| 500 mg | $942 | In Stock |
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Purity:99.29%
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All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.Product Introduction
Bioactivity
Chemical Properties
| Description | Butibufen (FF-106) is an orally active non-steroidal anti-inflammatory compound, a potential cyclooxygenase inhibitor with analgesic and antipyretic activity, and inhibits urea synthesis.Butibufen has been used in the study of rheumatic diseases. |
| In vitro | In hepatocytes from Sprague-Dawley male rats, Butibufen (0.1 μM-0.1 M; 60 min) exhibited no cell viability effects at a dose of 200 μM, but dose- and time-dependently affected cell viability at higher concentrations[2]. |
| In vivo | In Sprague-Dawley rats, Butibufen (50 and 250 mg/kg; oral gavage) reduces acid phosphatase activity but does not affect the stability of lysosomal membranes[3]. |
| Alias | FF-106, FF106, FF 106, FF 105 |
| Molecular Weight | 220.31 |
| Formula | C14H20O2 |
| Cas No. | 55837-18-8 |
Storage & Solubility Information
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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(mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.Preparation method for in vivo formula: Take 50 μL DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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