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Conditional PROTAC: Recent Strategies for Modulating Targeted Protein Degradation.
Yim, Junhyeong; Park, Junyoung; Kim, Gabin; Jo, Ala; Koh, Minseob; Park, Jongmin.
Afiliación
  • Yim J; Kangwon National University, Chemistry, KOREA, REPUBLIC OF.
  • Park J; Kangwon National University, chemistry, KOREA, REPUBLIC OF.
  • Kim G; Pusan National University, chemistry, KOREA, REPUBLIC OF.
  • Jo A; Institute for basic science, Center for Nanomedicine, KOREA, REPUBLIC OF.
  • Koh M; Pusan National University, Chemistry, KOREA, REPUBLIC OF.
  • Park J; Kangwon National University, Chemistry, Kangwondaehakgil 1, 24341, chuncheon, KOREA, REPUBLIC OF.
ChemMedChem ; : e202400326, 2024 Jul 12.
Article en En | MEDLINE | ID: mdl-38993102
ABSTRACT
Proteolysis-targeting chimeras (PROTACs) have emerged as a promising technology for inducing targeted protein degradation by leveraging the intrinsic ubiquitin-proteasome system (UPS). While the potential druggability of PROTACs toward undruggable proteins has accelerated their rapid development and the wide-range of applications across diverse disease contexts, off-tissue effect and side-effects of PROTACs have recently received attentions to improve their efficacy. To address these issues, spatial or temporal target protein degradation by PROTACs has been spotlighted. In this review, we explore chemical strategies for modulating protein degradation in a cell type-specific (spatio-) and time-specific (temporal-) manner, thereby offering insights for expanding PROTAC applications to overcome the current limitations of target protein degradation strategy.
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Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: ChemMedChem Asunto de la revista: FARMACOLOGIA / QUIMICA Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: ChemMedChem Asunto de la revista: FARMACOLOGIA / QUIMICA Año: 2024 Tipo del documento: Article