中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Synthesis and biological evaluation of novel amprenavir-based P1-substituted bi-aryl derivatives as ultra-potent HIV-1 protease inhibitors

文献类型:期刊论文

作者Yan JW1; Huang N2; Li SK1; Yang LM2; Xing WQ1; Zheng YT[*]2; Hu YH[*]1
刊名BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
出版日期2012
卷号22期号:5页码:1976-1979
关键词HIV-1 protease inhibitors Amprenavir Darunavir biaryl compounds Docking study
通讯作者zhengyt@mail.kiz.ac.cn ; yhhu@mail.shcnc.ac.cn
合作状况其它
英文摘要A series of P1-substituted biaryl amprenavir derivatives was designed and synthesized. These compounds were evaluated for enzyme inhibition and antiviral activity in vitro. Several compounds showed highly efficient antiviral activity with EC50 values down to 0.10 nM, which are more potent than marketed HIV-1 protease inhibitors. Docking study indicated that 12c has similar binding mode to amprenavir with full occupancy in P1.
收录类别SCI
资助信息This work was supported by the National Natural Science Foun- dation of China (Grant Nos.: 30600775, 81001462), the Eleventh Five-Year Key Scientific and Technological Program of China (2009ZX09501-029) and the CAS Knowledge Innovation Project (KSCX2-YW-R-185).
语种英语
WOS记录号WOS:000300451200028
公开日期2012-03-19
源URL[http://159.226.149.42:8088/handle/353002/6873]  
专题昆明动物研究所_分子免疫药理学
昆明动物研究所_动物模型与人类重大疾病机理重点实验室
作者单位1.State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 555 Zu Chong Zhi Road, Shanghai 201203, China
2.Key Laboratory of Animal Models and Human Disease Mechanisms of the Chinese Academy of Science & YunnanProvince, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming, Yunnan 650223, China
推荐引用方式
GB/T 7714
Yan JW,Huang N,Li SK,et al. Synthesis and biological evaluation of novel amprenavir-based P1-substituted bi-aryl derivatives as ultra-potent HIV-1 protease inhibitors[J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS,2012,22(5):1976-1979.
APA Yan JW.,Huang N.,Li SK.,Yang LM.,Xing WQ.,...&Hu YH[*].(2012).Synthesis and biological evaluation of novel amprenavir-based P1-substituted bi-aryl derivatives as ultra-potent HIV-1 protease inhibitors.BIOORGANIC & MEDICINAL CHEMISTRY LETTERS,22(5),1976-1979.
MLA Yan JW,et al."Synthesis and biological evaluation of novel amprenavir-based P1-substituted bi-aryl derivatives as ultra-potent HIV-1 protease inhibitors".BIOORGANIC & MEDICINAL CHEMISTRY LETTERS 22.5(2012):1976-1979.

入库方式: OAI收割

来源:昆明动物研究所

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