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Structure-Aided Identification and Optimization of Tetrahydro-isoquinolines as Novel PDE4 Inhibitors Leading to Discovery of an Effective Antipsoriasis Agent
2019-06-13
发表期刊JOURNAL OF MEDICINAL CHEMISTRY (IF:6.8[JCR-2023],7.1[5-Year])
ISSN0022-2623
卷号62期号:11页码:5579-5593
发表状态已发表
DOI10.1021/acs.jmedchem.9b00518
摘要Psoriasis is a common, chronic inflammatory disease characterized by abnormal skin plaques, and the effectiveness of phosphodiesterase 4 (PDE4) inhibitor to lessen the symptoms of psoriasis has been proved. Aiming to find a novel PDE4 inhibitor acting as an effective, safe, and convenient therapeutic agent, we constructed a library consisting of berberine analogues, and compound 2 with a tetrahydroisoquinoline scaffold was identified as a novel and potent hit. The structure-aided and cell-based structure-activity relationship studies on a series of tetrahydro-isoquinolines lead to efficient discovery of a qualified lead compound (16) with the high potency and selectivity, well characterized binding mechanism, high cell permeability, good safety and pharmacokinetic profile, and impressive in vivo efficacy on antipsoriasis, in particular with a topical application. Thus, our study presents a prime example for efficient discovery of novel, potent lead compounds derived from natural products using a combination of medicinal chemistry, biochemical, biophysical, and pharmacological approaches.
收录类别SCI ; SCIE ; IC
语种英语
资助项目Science & Technology Commission of Shanghai Municipality, China[19431901100] ; Science & Technology Commission of Shanghai Municipality, China[18431907100]
WOS研究方向Pharmacology & Pharmacy
WOS类目Chemistry, Medicinal
WOS记录号WOS:000471834500022
出版者AMER CHEMICAL SOC
WOS关键词PHOSPHODIESTERASE-4 INHIBITOR ; BERBERINE ; PSORIASIS ; MODEL ; INFLAMMATION ; MECHANISMS ; IMIQUIMOD ; PATHWAY ; MICE
原始文献类型Article
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文献类型期刊论文
条目标识符https://kms.shanghaitech.edu.cn/handle/2MSLDSTB/49483
专题生命科学与技术学院_硕士生
通讯作者Tang, Wei; Liu, Hong; Xu, Yechun
作者单位
1.Chinese Acad Sci, Shanghai Inst Mat Med, Lab Immunopharmacol,Drug Discovery & Design Ctr, State Key Lab Drug Res,CAS Key Lab Receptor Res, Shanghai 201203, Peoples R China
2.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
3.ShanghaiTech Univ, Sch Life Sci & Technol, Shanghai 201210, Peoples R China
4.Chinese Acad Sci, Shanghai Adv Res Inst, Shanghai Synchrotron Radiat Facil, Shanghai 201210, Peoples R China
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GB/T 7714
Zhang, Xianglei,Dong, Guangyu,Li, Heng,et al. Structure-Aided Identification and Optimization of Tetrahydro-isoquinolines as Novel PDE4 Inhibitors Leading to Discovery of an Effective Antipsoriasis Agent[J]. JOURNAL OF MEDICINAL CHEMISTRY,2019,62(11):5579-5593.
APA Zhang, Xianglei.,Dong, Guangyu.,Li, Heng.,Chen, Wuyan.,Li, Jian.,...&Xu, Yechun.(2019).Structure-Aided Identification and Optimization of Tetrahydro-isoquinolines as Novel PDE4 Inhibitors Leading to Discovery of an Effective Antipsoriasis Agent.JOURNAL OF MEDICINAL CHEMISTRY,62(11),5579-5593.
MLA Zhang, Xianglei,et al."Structure-Aided Identification and Optimization of Tetrahydro-isoquinolines as Novel PDE4 Inhibitors Leading to Discovery of an Effective Antipsoriasis Agent".JOURNAL OF MEDICINAL CHEMISTRY 62.11(2019):5579-5593.
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