| Field | Specification |
|---|---|
| CAS no. | |
| Applications | |
| Molecular weight | |
| Molecular formula | C12H12N4O6S |
| Purity | |
| SMILES | |
| Form | Solid |
| Storage | |
| Shipping | |
| Catalog no. (Mfr.) | |
| Main SKU |
Compound Overview
CN009543V is an agonist of the epidermal growth factor receptor (EGFR). It enhances tyrosine phosphorylation of EGFR at Tyr1068 and Tyr1173, activating the MAPK/ERK cascade, and it inhibits the activity of PTP-1B in MDA MB468 cells. The compound can be used in cancer research[1]. It is supplied as a light yellow to yellow solid (C12H12N4O6S, MW 340.31) at 99.37% purity.
Physical & Chemical Properties
| CAS Number | 375826-84-9 |
|---|---|
| Molecular Formula | C12H12N4O6S |
| Molecular Weight | 340.31 g/mol |
| Purity | 99.37% |
| Appearance | Solid |
| Color | Light yellow to yellow |
| SMILES | O=C(OC)C(CSC1=CC=C([N+]([O-])=O)C2=NON=C21)NC(C)=O |
| Signaling Pathway | JAK/STAT Signaling; Protein Tyrosine Kinase/RTK; MAPK/ERK Pathway; Stem Cell/Wnt; Metabolic Enzyme/Protease |
| Solubility | In Vitro: DMSO: 100 mg/mL (293.85 mM; Requires sonication; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO) |
| Storage | Powder: -20°C, 3 years; 4°C, 2 years. In solvent: -80°C, 6 months; -20°C, 1 month. |
| Shipping | Room temperature in continental US; may vary elsewhere. |
Literature Cited
Sources cited in this description. Peer-reviewed publications that used this product are listed under References.
Safety
For Research Use Only. Not for use in diagnostic or therapeutic procedures, and not for human or veterinary use. Handle in accordance with the Safety Data Sheet and your institution's chemical hygiene plan.
In Vitro
| Solvent | Solubility | Notes |
|---|---|---|
| DMSO | 100 mg/mL (293.85 mM) | requires sonication; use freshly opened DMSO (absorbed moisture lowers solubility) |
Aliquot the stock solution and store it at -80°C (up to 6 months) or -20°C (up to 1 month); avoid repeated freeze-thaw cycles.
In Vivo
Choose the formulation that suits the animal model and route of administration; percentages are volume ratios of the final working solution. Start from a clear DMSO stock (see In Vitro above), add the co-solvents one at a time in the order listed, mixing after each addition, and prepare the working solution fresh on the day of dosing. If precipitation or phase separation occurs, gentle warming or sonication can help.
Protocol 1
| Composition | 10% DMSO + 90% Corn Oil |
|---|---|
| Result | ≥ 5 mg/mL (14.69 mM); clear solution |
| How to prepare | Gives a clear solution at ≥ 5 mg/mL (saturation not determined). Use with caution if continuous dosing will exceed two weeks. For 1 mL of working solution: add 100 μL DMSO stock (50.0 mg/mL) to 900 μL corn oil. |
Data provided by the manufacturer.
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