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Recent Advances in the Discovery of CK2 Allosteric Inhibitors: From Traditional Screening to Structure-Based Design

Protein kinase (CK2) has emerged as an attractive cancer therapeutic target and recent efforts have been made to develop its inhibitors. However, the development of selective inhibitors remains challenging because of the highly conserved ATP-binding pocket (orthosteric site) of kinase family. As an...

詳細記述

保存先:
書誌詳細
出版年:Molecules
主要な著者: Chen, Xiaolan, Li, Chunqiong, Wang, Dada, Chen, Yu, Zhang, Na
フォーマット: Artigo
言語:Inglês
出版事項: MDPI 2020
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC7070378/
https://ncbi.nlm.nih.gov/pubmed/32079098
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/molecules25040870
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