4.6 Review

Inside Perspective of the Synthetic and Computational Toolbox of JAK Inhibitors: Recent Updates

期刊

MOLECULES
卷 25, 期 15, 页码 -

出版社

MDPI
DOI: 10.3390/molecules25153321

关键词

Janus kinase (JAK); multitarget; inflammation; cancer; synthetic strategies; tofacitinib; ruxolitinib

资金

  1. MIUR research project [NUTRAMED PON 03PE000_78_2]

向作者/读者索取更多资源

The mechanisms of inflammation and cancer are intertwined by complex networks of signaling pathways. Dysregulations in the Janus kinase/signal transducer and activator of transcription (JAK/STAT) pathway underlie several pathogenic conditions related to chronic inflammatory states, autoimmune diseases and cancer. Historically, the potential application of JAK inhibition has been thoroughly explored, thus triggering an escalation of favorable results in this field. So far, five JAK inhibitors have been approved by the Food and Drug Administration (FDA) for the treatment of different diseases. Considering the complexity of JAK-depending processes and their involvement in multiple disorders, JAK inhibitors are the perfect candidates for drug repurposing and for the assessment of multitarget strategies. Herein we reviewed the recent progress concerning JAK inhibition, including the innovations provided by the release of JAKs crystal structures and the improvement of synthetic strategies aimed to simplify of the industrial scale-up.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据