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Synonyms: O-glycosylation-IN-1


| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 5 mg | $40 | In Stock | In Stock | |
| 10 mg | $64 | In Stock | In Stock | |
| 25 mg | $129 | In Stock | In Stock | |
| 50 mg | $198 | In Stock | In Stock | |
| 100 mg | $328 | In Stock | In Stock | |
| 200 mg | $492 | In Stock | In Stock | |
| 1 mL x 10 mM (in DMSO) | $44 | In Stock | In Stock |
| Description | Benzyl-α-GalNAc (O-glycosylation-IN-1) is an effective inhibitor of O-glycosylation used to reduce the levels of mucin on the cell surface; it can inhibit the synthesis of O-glycosylated mucin in a human pancreatic cancer cell model. Benzyl-α-GalNAc effectively inhibits the proliferation and activation of LX-2 cells and suppresses the expression of collagen I/III, making it suitable for studies on liver fibrosis. Benzyl-α-GalNAc can be used in research on glycobiology, tumor metastasis, liver fibrosis, and chemotherapeutic sensitization. |
| In vitro | Methods: Benzyl-α-GalNAc (2.5 mM) was added to cerebellar granule neurons from newborn (P5-7) SD rats and incubated for 48 hours. Western blot analysis was performed to validate the salicylate modification level of O-linked glycoproteins in cell lysates using biotinylated PNA. Results: Benzyl-α-GalNAc treatment resulted in a significant increase (>4-fold) in PNA binding in cell lysates, confirming its effective inhibition of O-linked glycosylation. [1] |
| In vivo | Methods: Male C57BL/6 mice aged 6–8 weeks were fed a high-fat diet (HFD) for 10 weeks to induce a metabolic syndrome-like liver disease (MASLD) model. Following 10 weeks of HFD feeding, mice received consecutive tail vein injections of Benzyl-α-GalNAc (0.5, 1.0, 2.0 mg/mouse) daily for 4 weeks. Results: Benzyl-α-GalNAc dose-dependently reduced total hepatic O-GlcNAc and HNF1α O-GlcNAc levels, decreased serum ALT, AST, and TG levels, and alleviated hepatic lipid deposition, collagen deposition, and HSC activation (α-SMA).[1] |
| Synonyms | O-glycosylation-IN-1 |
| Molecular Weight | 311.33 |
| Formula | C15H21NO6 |
| Cas No. | 3554-93-6 |
| Smiles | CC(=O)N[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@@H]1OCc1ccccc1 |
| Relative Density. | 1.34 g/cm3 (Predicted) |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. | ||||||||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 240 mg/mL (770.89 mM), Sonication is recommended. H2O: 8.33 mg/mL (26.76 mM), Sonication is recommended. | ||||||||||||||||||||||||||||||||||||||||
| In Vivo Formulation | 10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (6.42 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 | |||||||||||||||||||||||||||||||||||||||||
H2O/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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