| Name | RR-11a |
|---|
| Description | RR-11a is a synthetic enzyme inhibitor of Legumain. |
|---|---|
| Related Catalog | |
| Target |
Legumain[1] |
| In Vitro | Legumain-targeted RR-11a-coupled nanoparticles reveal high ligand-receptor affinity, enhance solid-tumor penetration and uptake by tumor cells[1]. |
| In Vivo | Treatment of tumor-bearing mice with RR-11a-coupled NPs encapsulating doxorubicin results in improved tumor selectivity and drug sensitivity, leading to complete inhibition of tumor growth[1]. |
| Animal Admin | Mice[1] Mice bearing 4T1 orthothopic tumors of approximately 500 mm3 are injected once intravenously with RR-11a+ or RR-11a-nanoparticles labeled with rhodamine B. Alternatively, mice are injected intravenously 3 times at 48-hour intervals with RDZ-218, NP-DOX, free DOX, or saline. Twenty-four hours after the final treatment, animals are sacrificed and spleen, kidney, lungs, liver, heart and tumor are collected, frozen in OCT compound, immediately sectioned and imaged by fluorescence microscopy[1]. |
| References |
| Molecular Formula | C24H28N6O10 |
|---|---|
| Molecular Weight | 560.51 |