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α-L-fucopyranose, an endogenous metabolite and six-carbon deoxyhexose, is present at the terminal or anterior position of many cell surface oligosaccharide ligands, mediates cell recognition and adhesion signaling pathways, and is a potentially critical molecule in pathological processes, including tumors.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $195 | - | In Stock | |
| 5 mg | $483 | - | In Stock | |
| 10 mg | $692 | - | In Stock | |
| 25 mg | $1,080 | - | In Stock | |
| 50 mg | $1,490 | - | In Stock | |
| 100 mg | $1,970 | - | In Stock | |
| 200 mg | $2,690 | - | In Stock |
| Description | α-L-fucopyranose, an endogenous metabolite and six-carbon deoxyhexose, is present at the terminal or anterior position of many cell surface oligosaccharide ligands, mediates cell recognition and adhesion signaling pathways, and is a potentially critical molecule in pathological processes, including tumors. |
| In vitro | Methods: RAW264.7 macrophages were treated with α-L-Fucopyranos (5 mg/ml, 10 mg/ml, 4 hours), and the cells were collected to quantify the levels of IL-6 and MCP-1 by qPCR. Results: Quantitative PCR Results showed that the levels of Mcp1 and Il6 decreased in a concentration-dependent manner in RAW264.7 cells (Figure 5C), indicating that α-L-Fucopyranos can alleviate inflammation in vivo and in vitro. [2] |
| In vivo | Methods: α-L-Fucopyranos (100 mg/kg, intraperitoneal injection, three times a week) was used to treat HuCCT-1 cell-transplanted tumor model mice, and tumor volume and body weight were measured daily. Results: Tumor size, angiogenesis, and stiffness index were reduced in the α-L-Fucopyranos-treated group, indicating that α-L-Fucopyranos can inhibit tumor growth in mice. [3] |
| Synonyms | α-L-Fucose, Deoxy-a-L-galactopyranose, Alpha-L-Fucose, Alpha-L-Fucopyranose |
| Molecular Weight | 164.16 |
| Formula | C6H12O5 |
| Cas No. | 6696-41-9 |
| Smiles | O[C@H]1[C@@H](O)[C@H](O)[C@H](O)O[C@H]1C |
| Storage | store under nitrogen | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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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