Design and synthesis of cinanserin analogs as severe acute respiratory syndrome coronavirus 3CL protease inhibitors | |
Yang, Qiangang2; Chen, Lill2; He, Xuchang2; Gao, Zhenting1; Bai, Donglu2 | |
刊名 | CHEMICAL & PHARMACEUTICAL BULLETIN |
2008-10 | |
卷号 | 56期号:10页码:1400-1405 |
关键词 | SARS coronavirus 3CL protease cinanserin analogs inhibitor fluorescence resonance energy transfer-based assay |
ISSN号 | 0009-2363 |
DOI | 10.1248/cpb.56.1400 |
文献子类 | Article |
英文摘要 | The severe acute respiratory syndrome (SARS) coronavirus 3CL protease is an attractive target for the development of anti-SARS drugs. In this paper, cinanserin (1) analogs were synthesized and tested for the in-hibitory activities against SARS-coronavirus (CoV) 3CL protease by fluorescence resonance energy transfer (FRET) assay. Four analogs show significant activities, especially compound 26 with an IC50 of 1.06 mu M. |
WOS关键词 | SARS CORONAVIRUS ; 3C-LIKE PROTEINASE ; GENOME SEQUENCE ; DERIVATIVES |
WOS研究方向 | Pharmacology & Pharmacy ; Chemistry |
语种 | 英语 |
出版者 | PHARMACEUTICAL SOC JAPAN |
WOS记录号 | WOS:000259672800005 |
内容类型 | 期刊论文 |
源URL | [http://119.78.100.183/handle/2S10ELR8/272790] |
专题 | 院士及顾问专家 |
通讯作者 | Bai, Donglu |
作者单位 | 1.E China Univ Sci & Technol, Sch Pharm, Shanghai 200237, Peoples R China 2.Chinese Acad Sci, Shanghai Inst Mat Med, Shanghai 201203, Peoples R China; |
推荐引用方式 GB/T 7714 | Yang, Qiangang,Chen, Lill,He, Xuchang,et al. Design and synthesis of cinanserin analogs as severe acute respiratory syndrome coronavirus 3CL protease inhibitors[J]. CHEMICAL & PHARMACEUTICAL BULLETIN,2008,56(10):1400-1405. |
APA | Yang, Qiangang,Chen, Lill,He, Xuchang,Gao, Zhenting,&Bai, Donglu.(2008).Design and synthesis of cinanserin analogs as severe acute respiratory syndrome coronavirus 3CL protease inhibitors.CHEMICAL & PHARMACEUTICAL BULLETIN,56(10),1400-1405. |
MLA | Yang, Qiangang,et al."Design and synthesis of cinanserin analogs as severe acute respiratory syndrome coronavirus 3CL protease inhibitors".CHEMICAL & PHARMACEUTICAL BULLETIN 56.10(2008):1400-1405. |
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