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ShanghaiTech University Knowledge Management System
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]) |
ISSN | 0022-2623 |
卷号 | 62期号:11页码:5579-5593 |
发表状态 | 已发表 |
DOI | 10.1021/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 |
引用统计 | 正在获取...
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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 |
推荐引用方式 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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