期刊
JOURNAL OF MEDICINAL CHEMISTRY
卷 65, 期 24, 页码 16622-16639出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.jmedchem.2c01444
关键词
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资金
- Jiangsu Natural Science Foundation [BK20202009]
- National Natural Science Foundation of China [82273799, 81730094, 81773584, 21977118]
- Chongqing Talent Program [cstc2022ycjh-bgzxm0197]
- Natural Science Foundation of Chongqing [CSTB2022NSCQ-MSX1649]
USP7 has been identified as a potential therapeutic target for cancer due to its role in tumor development. However, finding drug-like USP7 inhibitors remains challenging. This study reports a series of N-benzylpiperidinol derivatives as potent and selective USP7 inhibitors, which exhibit significant antitumor activity and may have potential as novel cancer immunotherapy drugs.
USP7 emerges as a potential therapeutic target for cancers, as it plays an important role in the development of tumorigenesis by stabilizing multiple cancer-relevant proteins. Nevertheless, the discovery of drug-like USP7 inhibitors remains challenging. Herein, we report a series of N-benzylpiperidinol derivatives as potent and selective USP7 inhibitors (e.g., X20 and X26: IC50 = 7.6 and 8.2 nM), whose binding modes were revealed by crystallographic studies to be distinct from the known N- acylpiperidinol USP7 inhibitors. Among them, X36 with good oral PK profiles (rat: F = 40.8% and T1/2 = 3.5 h) exhibited significant antitumor efficacy in the MC38 colon cancer syngeneic mouse model, at least partly through upregulating the tumor infiltration of CD8+ T, NK, and NKT cells and downregulating that of Tregs and MDSCs. These findings may further pave the way for the development of USP7 inhibitors as novel cancer immunotherapy drugs.
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