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| Product Name | Tanspiramycin (17-AAG)lipid nanoparticle |
| Catalog Number | LNP-010 |
| Size | 10 mg; 20 mg; 50 mg |
| Alias | Tanespimycin (17-AAG)LNP; Geldanamycin derivative lipid nanoparticle delivery system |
| Appearance | Light yellow to amber homogeneous suspension |
| Solubility | It can be dispersed in physiological buffer or 5% glucose solution to form a stable colloidal dispersion system |
| Description | Tanespimycin (17-AAG)LNP is a specialized nano-lipid nanoparticle formulation of the heat shock protein 90 inhibitor tanspiromycin (tanespimycin, 17-AAG). 17-AAG, as a water-soluble derivative of geldanamycin, specifically binds to the ATP-binding pocket of HSP90 and induces the ubiquitination and degradation of its proteins (such as various kinases and transcription factors), thereby interfering with the proliferation, survival and metastasis signaling pathways of tumor cells. Although its water solubility is improved compared with the parent compound, it still faces challenges such as insufficient solubility, rapid metabolism in the body, and lack of tumor targeting. |
| Applications | Development of nano-delivery system for poorly soluble HSP90 inhibitors |
| Storage | 4°C, protected from light |
| Purity | 95%+ |
| Shelf Life | 1 Year |
| Shipping Condition | Low temperature transport |