ATP柠檬酸裂解酶
裂解酶
化学
虚拟筛选
酶
生物化学
糖酵解
计算生物学
癌症研究
药物发现
柠檬酸合酶
生物
作者
Jian-Jia Liang,Xiang-Feng Zhou,Hui Long,Chengpeng Li,Jing Wei,Xiaoqin Yu,Zhiyong Guo,Yiqing Zhou,Zhangshuang Deng
标识
DOI:10.1016/j.bioorg.2023.106933
摘要
ATP citrate lyase (ACLY), a strategic metabolic enzyme that catalyzes the glycolytic to lipidic metabolism, has gained increasing attention as an attractive therapeutic target for hyperlipidemia, cancers and other human diseases. Despite of continual research efforts, targeting ACLY has been very challenging. In this field, most reported ACLY inhibitors are “substrate-like” analogues, which occupied with the same active pockets. Besides, some ACLY inhibitors have been disclosed through biochemical screening or high throughput virtual screening. In this review, we briefly summarized the cancer-related functions and the recent advance of ACLY inhibitors with a particular focus on the SAR studies and their modes of action. We hope to provide a timely and updated overview of ACLY and the discovery of new ACLY inhibitors.
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