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Kaempferol 3-O-β-D-galactopyranoside
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Catalog No. TN1823Cas No. 23627-87-4
Alias Kaempferol-3-O-galactoside, Kaempferol 3-O-beta-D-galactoside
Kaempferol 3-O-β-D-galactopyranoside possesses antioxidant, anti-inflammatory, and antinociceptive activities.
Kaempferol 3-O-β-D-galactopyranoside
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Purity: 99.22%
Catalog No. TN1823Alias Kaempferol-3-O-galactoside, Kaempferol 3-O-beta-D-galactosideCas No. 23627-87-4
Kaempferol 3-O-β-D-galactopyranoside possesses antioxidant, anti-inflammatory, and antinociceptive activities.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $128 | - | In Stock | |
| 5 mg | $289 | - | In Stock | |
| 10 mg | $455 | - | In Stock | |
| 25 mg | $733 | - | In Stock | |
| 50 mg | $987 | - | In Stock | |
| 1 mL x 10 mM (in DMSO) | $333 | - | In Stock |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Batch Information
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Purity:99.22%
Appearance:Solid
Color:White to Yellow
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Product Introduction
Kaempferol 3-O-β-D-galactopyranoside AI Summary
Kaempferol 3-O-β-D-galactopyranoside displays a variety of bioactivities, showing potential as an inhibitor and therapeutic agent. It inhibits cow milk xanthine oxidase with 16.1% inhibition at 50 µg/mL, indicating its role in mitigating oxidative stress and purine metabolism disorders. The compound also has notable antiviral activity, particularly against RSV Long and PIV3, with IC50 values of 71.7 µg/mL and 53.8 µg/mL, respectively. However, it shows limited effectiveness against influenza virus type A H1N1 with an IC50 greater than 300.0 µg/mL. Cytotoxicity against MDCK cells is noted with an IC50 of 143.3 µg/mL. Additionally, Kaempferol 3-O-β-D-galactopyranoside exhibits moderate antileishmanial activity against Leishmania peruviana and Leishmania braziliensis promastigotes with IC50 values of 53340.0 nM and 52460.0 nM, respectively, and cytotoxicity to BALB/c mouse J774.2 cells with an IC50 of 161320.0 nM. It inhibits rabbit lung ACE with an IC50 of 260,000.0 nM and demonstrates inhibition of Saccharomyces cerevisiae alcohol dehydrogenase at an IC50 of 70300.0 nM. Moreover, the compound shows antioxidant activity via DPPH radical scavenging, albeit with limited efficacy (4.5% inhibition at 250 µM and an IC50 greater than 100000.0 nM). Lastly, it exhibits hepatoprotective activity in Wistar rat hepatocytes against tert-butyl hydroperoxide-induced oxidative stress, enhancing cell viability to 191.0% at 60 µg/mL. These multifaceted activities highlight Kaempferol 3-O-β-D-galactopyranoside's potential in various therapeutic contexts..
Note: Summary generated by AI. Data source: ChEMBL 
Bioactivity
Chemical Properties
Storage & Solubility Information
| Description | Kaempferol 3-O-β-D-galactopyranoside possesses antioxidant, anti-inflammatory, and antinociceptive activities. |
| Synonyms | Kaempferol-3-O-galactoside, Kaempferol 3-O-beta-D-galactoside |
| Molecular Weight | 448.38 |
| Formula | C21H20O11 |
| Cas No. | 23627-87-4 |
| Smiles | OC[C@H]1O[C@@H](Oc2c(oc3cc(O)cc(O)c3c2=O)-c2ccc(O)cc2)[C@H](O)[C@@H](O)[C@H]1O |
| Relative Density. | 1.79 g/cm3 at 20℃ |
| Storage | store at low temperature,keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 60 mg/mL (133.82 mM), Sonication is recommended.  | |||||||||||||||||||||||||||||||||||
| In Vivo Formulation | 10% DMSO+40% PEG300+5% Tween 80+45% Saline: 1 mg/mL (2.23 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 | ||||||||||||||||||||||||||||||||||||
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Calculator
In Vivo Formulation Calculator (Clear solution)
Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, and a total of 10 animals are to be administered, using a formulation of 
10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.Stock Solution Preparation:
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.
Preparation of the In Vivo Formulation:
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.
This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
Dose Conversion
You can also refer to dose conversion for different animals. More Dose Conversion
Tech Support
Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
Keywords
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