1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine-N-[3-(2-pyridyldithio)propionate] (sodium salt)
>99%
- Product Code: 62412
CAS:
474944-16-6
| Molecular Weight: | 912.2300 g./mol | Molecular Formula: | C₄₅H₈₁N₂O₉PS₂Na |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20℃ |
Product Description:
This chemical is widely used in bioconjugation and drug delivery systems due to its ability to form stable disulfide bonds with thiol-containing molecules. It is particularly valuable in the development of targeted therapeutic agents, such as antibody-drug conjugates (ADCs), where it serves as a linker to attach cytotoxic drugs to antibodies. The disulfide bond allows for controlled release of the drug in the reducing environment of target cells, enhancing specificity and minimizing off-target effects. Additionally, it is employed in liposome formulations to improve the stability and functionality of lipid-based delivery systems, enabling efficient transport of therapeutic agents to specific tissues or cells. Its application extends to research in biochemistry and molecular biology for labeling and cross-linking proteins or peptides, facilitating studies on protein interactions and cellular processes.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Light Yellow Flakes |
| PURITY | 98.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | ฿60,840.00 |
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1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine-N-[3-(2-pyridyldithio)propionate] (sodium salt)
This chemical is widely used in bioconjugation and drug delivery systems due to its ability to form stable disulfide bonds with thiol-containing molecules. It is particularly valuable in the development of targeted therapeutic agents, such as antibody-drug conjugates (ADCs), where it serves as a linker to attach cytotoxic drugs to antibodies. The disulfide bond allows for controlled release of the drug in the reducing environment of target cells, enhancing specificity and minimizing off-target effects. Additionally, it is employed in liposome formulations to improve the stability and functionality of lipid-based delivery systems, enabling efficient transport of therapeutic agents to specific tissues or cells. Its application extends to research in biochemistry and molecular biology for labeling and cross-linking proteins or peptides, facilitating studies on protein interactions and cellular processes.
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