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Targeted Degradation of Oncogenic KRAS(G12C) by VHL-Recruiting PROTACs

[Image: see text] KRAS is mutated in ∼20% of human cancers and is one of the most sought-after targets for pharmacological modulation, despite having historically been considered “undruggable.” The discovery of potent covalent inhibitors of the KRAS(G12C) mutant in recent years has sparked a new wav...

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Detalhes bibliográficos
Publicado no:ACS Cent Sci
Main Authors: Bond, Michael J., Chu, Ling, Nalawansha, Dhanusha A., Li, Ke, Crews, Craig M.
Formato: Artigo
Idioma:Inglês
Publicado em: American Chemical Society 2020
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7453568/
https://ncbi.nlm.nih.gov/pubmed/32875077
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/acscentsci.0c00411
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