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Peptidylarginine deiminases 4 as a promising target in drug discovery.
Yang, Chao; Dong, Zhen-Zhen; Zhang, Jing; Teng, Dehong; Luo, Xinzhi; Li, Dan; Zhou, Yingtang.
Afiliação
  • Yang C; National Engineering Research Center for Marine Aquaculture, Institute of Innovation & Application, Zhejiang Ocean University, Zhoushan, Zhejiang Province, 316022, China.
  • Dong ZZ; Department of Chemistry, Hong Kong Baptist University, Kowloon Tong, Hong Kong, China.
  • Zhang J; National Engineering Research Center for Marine Aquaculture, Institute of Innovation & Application, Zhejiang Ocean University, Zhoushan, Zhejiang Province, 316022, China.
  • Teng D; National Engineering Research Center for Marine Aquaculture, Institute of Innovation & Application, Zhejiang Ocean University, Zhoushan, Zhejiang Province, 316022, China.
  • Luo X; National Engineering Research Center for Marine Aquaculture, Institute of Innovation & Application, Zhejiang Ocean University, Zhoushan, Zhejiang Province, 316022, China.
  • Li D; State Key Laboratory of Southwestern Chinese Medicine Resources, School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu, China. Electronic address: lidan@cdutcm.edu.cn.
  • Zhou Y; National Engineering Research Center for Marine Aquaculture, Institute of Innovation & Application, Zhejiang Ocean University, Zhoushan, Zhejiang Province, 316022, China. Electronic address: zhouyingtang@zjou.edu.cn.
Eur J Med Chem ; 226: 113840, 2021 Dec 15.
Article em En | MEDLINE | ID: mdl-34520958
ABSTRACT
Peptidylarginine deaminase 4 (PAD4) is a crucial post-translational modifying enzyme catalyzing the conversion of arginine into citrulline residues, and mediating the formation of neutrophil extracellular traps (NETs). PAD4 plays a vital role in the occurrence and development of cardiovascular diseases, autoimmune diseases, and various tumors. Therefore, PAD4 is considered as a promising drug target for disease diagnosis and treatment. More and more efforts are devoted to developing highly efficient and selective PAD4 inhibitors via high-throughput screening, structure-based drug design and structure-activity relationship study. This article outlined the physiological and pathological functions of PAD4, and corresponding representative small molecule inhibitors reported in recent years.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Inibidores Enzimáticos / Descoberta de Drogas / Proteína-Arginina Desiminase do Tipo 4 Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Inibidores Enzimáticos / Descoberta de Drogas / Proteína-Arginina Desiminase do Tipo 4 Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article