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Tumor Targeting with an isoDGR–Drug Conjugate
Herein we report the first example of an isoDGR–drug conjugate (2), designed to release paclitaxel selectively within cancer cells expressing integrin α(V)β(3). Conjugate 2 was synthesized by connecting the isoDGR peptidomimetic 5 with paclitaxel via the lysosomally cleavable Val–Ala dipeptide linke...
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| Publicado en: | Chemistry |
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| Autores principales: | , , , , , , , , , , , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
John Wiley and Sons Inc.
2017
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5488297/ https://ncbi.nlm.nih.gov/pubmed/28449309 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/chem.201701844 |
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