中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Recent progress and challenges in screening and characterization of ugt1a1 inhibitors

文献类型:期刊论文

作者Lv, Xia1,2; Xia, Yangliu3; Finel, Moshe4; Wu, Jingjing3; Ge, Guangbo1,3; Yang, Ling1
刊名Acta pharmaceutica sinica b
出版日期2019-03-01
卷号9期号:2页码:258-278
关键词Ugt1a1 inhibitors Drug/herbdrug interactions Probe substrates High-throughput screening
ISSN号2211-3835
DOI10.1016/j.apsb.2018.09.005
通讯作者Ge, guangbo(geguangbo@shutcm.edu.cn)
英文摘要Uridine-diphosphate glucuronosyltransferase 1a1 (ugt1a1) is an important conjugative enzyme in mammals that is responsible for the conjugation and detoxification of both endogenous and xenobiotic compounds. strong inhibition of ugt1a1 may trigger adverse drug/herb-drug interactions, or result in metabolic disorders of endobiotic metabolism. therefore, both the us food and drug administration (fda) and the european medicines agency (ema) have recommended assaying the inhibitory potential of drugs under development on the human ugt1a1 prior to approval. this review focuses on the significance, progress and challenges in discovery and characterization of ugt1a1 inhibitors. recent advances in the development of ugt1a1 probes and their application for screening ugt1a1 inhibitors are summarized and discussed in this review for the first time. furthermore, a long list of ugt1a1 inhibitors, including information on their inhibition potency, inhibition mode, and affinity, has been prepared and analyzed. challenges and future directions in this field are highlighted in the final section. the information and knowledge that are presented in this review provide guidance for rational use of drugs/herbs in order to avoid the occurrence of adverse effects via ugt1a1 inhibition, as well as presenting methods for rapid screening and characterization of ugt1a1 inhibitors and for facilitating investigations on ugt1a1-ligand interactions. (c) 2019 chinese pharmaceutical association and institute of materia medica, chinese academy of medical sciences. production and hosting by elsevier b.v.
WOS关键词UDP-GLUCURONOSYLTRANSFERASE 1A1 ; HUMAN LIVER-MICROSOMES ; RATIOMETRIC FLUORESCENT-PROBE ; PRIMARY HUMAN HEPATOCYTES ; HUMAN CARBOXYLESTERASE 2 ; IN-VITRO INHIBITION ; BILIRUBIN GLUCURONIDATION ; GENETIC-POLYMORPHISM ; DRUG-INTERACTIONS ; ENZYME-ACTIVITIES
WOS研究方向Pharmacology & Pharmacy
WOS类目Pharmacology & Pharmacy
语种英语
WOS记录号WOS:000461052500004
出版者INST MATERIA MEDICA, CHINESE ACAD MEDICAL SCIENCES
URI标识http://www.irgrid.ac.cn/handle/1471x/2372715
专题大连化学物理研究所
通讯作者Ge, Guangbo
作者单位1.Shanghai Univ Tradit Chinese Med, Inst Interdisciplinary Med, Shanghai 201203, Peoples R China
2.Dalian Minzu Univ, Coll Life Sci, Minist Educ, Key Lab Biotechnol & Bioresources Utilizat, Dalian 116600, Peoples R China
3.Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
4.Univ Helsinki, Div Pharmaceut Chem & Technol, Fac Pharm, Helsinki, Finland
推荐引用方式
GB/T 7714
Lv, Xia,Xia, Yangliu,Finel, Moshe,et al. Recent progress and challenges in screening and characterization of ugt1a1 inhibitors[J]. Acta pharmaceutica sinica b,2019,9(2):258-278.
APA Lv, Xia,Xia, Yangliu,Finel, Moshe,Wu, Jingjing,Ge, Guangbo,&Yang, Ling.(2019).Recent progress and challenges in screening and characterization of ugt1a1 inhibitors.Acta pharmaceutica sinica b,9(2),258-278.
MLA Lv, Xia,et al."Recent progress and challenges in screening and characterization of ugt1a1 inhibitors".Acta pharmaceutica sinica b 9.2(2019):258-278.

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来源:大连化学物理研究所

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