中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Biological Function of Pin1 in Vivo and Its Inhibitors for Preclinical Study: Early Development, Current Strategies, and Future Directions

文献类型:期刊论文

作者He, Siyu1; Li, Linjie2; Jin, Rui2; Lu, Xiaojie2,3,4
刊名JOURNAL OF MEDICINAL CHEMISTRY
出版日期2023-07-13
卷号66期号:14页码:9251-9277
ISSN号0022-2623
DOI10.1021/acs.jmedchem.3c00390
通讯作者Li, Linjie(linjieli816@163.com) ; Lu, Xiaojie(xjlu@simm.ac.cn)
英文摘要Peptidyl-prolyl cis/trans isomerase family (PPIase) isstructurallydivided into three subfamilies, cyclophilins (Cyps), FK506-bindingproteins (FKBPs), and parvulins. Pin1 belongs to the parvulin familyand is the only enzyme capable of isomerizing the phosphorylated Ser/Thr-Promotif (p-Ser/Thr-Pro) in its interacting proteins. Due to its multibiologicalfunctions in vivo, including folding, intracellular signaling, transcription,cell cycle progression, and apoptosis, Pin1 is extensively studiedas a promising drug target for various human diseases, especiallycancer. In this Perspective, we summarized the literature coveringdiverse classes of Pin1 inhibitors and the inhibition mechanism, aimingto provide insights for the design of potent Pin1 inhibitors and suggestalternative strategies for developing potent Pin1 inhibitors.
WOS关键词PROLYL-ISOMERASE PIN1 ; ACUTE PROMYELOCYTIC LEUKEMIA ; STRUCTURE-BASED DESIGN ; NIMA-INTERACTING 1 ; TRANSCRIPTIONAL ACTIVITY ; BETA-CATENIN ; CELL-CYCLE ; PROTEIN-PHOSPHORYLATION ; SUBSTRATE RECOGNITION ; CONFORMATIONAL-CHANGE
资助项目Shanghai Municipal Science and Technology Major Project[NSFC-91953203] ; Shanghai Municipal Science and Technology Major Project[NSFC-21877117]
WOS研究方向Pharmacology & Pharmacy
语种英语
出版者AMER CHEMICAL SOC
WOS记录号WOS:001024839700001
源URL[http://119.78.100.183/handle/2S10ELR8/306439]  
专题新药研究国家重点实验室
通讯作者Li, Linjie; Lu, Xiaojie
作者单位1.Shanghai Univ, Sch Life Sci, Shanghai 200444, Peoples R China
2.Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai 201203, Peoples R China
3.Nanjing Univ Chinese Med, Sch Chinese Mat Med, Nanjing 210023, Peoples R China
4.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
推荐引用方式
GB/T 7714
He, Siyu,Li, Linjie,Jin, Rui,et al. Biological Function of Pin1 in Vivo and Its Inhibitors for Preclinical Study: Early Development, Current Strategies, and Future Directions[J]. JOURNAL OF MEDICINAL CHEMISTRY,2023,66(14):9251-9277.
APA He, Siyu,Li, Linjie,Jin, Rui,&Lu, Xiaojie.(2023).Biological Function of Pin1 in Vivo and Its Inhibitors for Preclinical Study: Early Development, Current Strategies, and Future Directions.JOURNAL OF MEDICINAL CHEMISTRY,66(14),9251-9277.
MLA He, Siyu,et al."Biological Function of Pin1 in Vivo and Its Inhibitors for Preclinical Study: Early Development, Current Strategies, and Future Directions".JOURNAL OF MEDICINAL CHEMISTRY 66.14(2023):9251-9277.

入库方式: OAI收割

来源:上海药物研究所

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