Recent advances in structural types and medicinal chemistry of PARP-1 inhibitors

被引:0
|
作者
Ling Yu
Zhi-wei Yan
You-de Wang
Hao Miao
Jing-yi Zhao
Chong Pang
Shuai Li
机构
[1] Anorectal Hospital of Chengde Medical University,Department of Pharmacy
[2] Chengde Medical University,Key Laboratory of Traditional Chinese Medicine Research and Development of Hebei Province, Institute of Traditional Chinese Medicine
[3] Chengde Medical University,School of basic medical sciences
来源
关键词
PARP-1 inhibitors; Cancer; Structural types; Characteristics; Biological activity;
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学科分类号
摘要
Poly (ADP-ribose) Polymerase-1 (PARP-1) is a member of 17 membered PARP family having diversified biological functions such as synthetic lethality, DNA repair, apoptosis, necrosis and histone binding, etc. The U.S. FDA has approved four PARP-1 inhibitors, namely Olaparib, Rucaparib, Niraparib, and Talazoparib. And, Veliparib has entered the late stage of clinical research as a PARP-1 inhibitor. At present, PARP-1 inhibitors have been approved for ovarian cancer, breast cancer, pancreatic cancer and other related indications. In recent years, more and more novel PARP-1 inhibitors have been reported. This review has attempted to summarize the structural types and characteristics of various novel PARP-1 inhibitors reported since 2020. And we outlined the current clinical application potential of PARP-1 inhibitors and further analyzed its current challenges and future development trends.
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页码:1265 / 1276
页数:11
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