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JNK3 inhibitors as promising pharmaceuticals with neuroprotective properties.
Wu, Yibeini; Zhao, Yiling; Guan, Ziman; Esmaeili, Sajjad; Xiao, Zhicheng; Kuriakose, Diji.
Afiliação
  • Wu Y; Department of Anatomy and Developmental biology, Monash University, Clayton, Vic, Australia.
  • Zhao Y; Shaoxing Institute, Zhejiang University, Shaoxing, China.
  • Guan Z; Department of Anatomy and Developmental biology, Monash University, Clayton, Vic, Australia.
  • Esmaeili S; Department of Anatomy and Developmental biology, Monash University, Clayton, Vic, Australia.
  • Xiao Z; Department of Anatomy and Developmental biology, Monash University, Clayton, Vic, Australia.
  • Kuriakose D; Shaoxing Institute, Zhejiang University, Shaoxing, China.
Cell Adh Migr ; 18(1): 1-11, 2024 Dec.
Article em En | MEDLINE | ID: mdl-38357988
ABSTRACT
The intensive study and investigation of neuroprotective therapy for central nervous system (CNS) diseases is ongoing. Due to shared mechanisms of neurodegeneration, a neuroprotective approach might offer benefits across multiple neurological disorders, despite variations in symptoms or injuries. C-Jun N-terminal Kinase 3 (JNK3) is found primarily in the CNS and is involved in physiological processes such as brain development, synapse formation, and memory formation. The potential of JNK3 as a target for pharmacological development holds promise for advancing neuroprotective therapies. Developing small molecule JNK3 inhibitors into drugs with neuroprotective qualities could facilitate neuronal restoration and self-repair. This review focuses on elucidating key neuroprotective mechanisms, exploring the interplay between neurodegenerative diseases and neuroprotection, and discussing advancements in JNK3 inhibitor drug development.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteína Quinase 10 Ativada por Mitógeno / Neuroproteção Idioma: En Revista: Cell Adh Migr Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteína Quinase 10 Ativada por Mitógeno / Neuroproteção Idioma: En Revista: Cell Adh Migr Ano de publicação: 2024 Tipo de documento: Article