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Artificial Macrocycles as Potent p53–MDM2 Inhibitors
[Image: see text] Based on a combination of an Ugi four component reaction and a ring closing metathesis, a library of novel artificial macrocyclic inhibitors of the p53–MDM2 interaction was designed and synthesized. These macrocycles, alternatively to stapled peptides, target for the first time the...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
American Chemical
Society
2017
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5641952/ https://www.ncbi.nlm.nih.gov/pubmed/29057045 http://dx.doi.org/10.1021/acsmedchemlett.7b00219 |