Progress in the fragment-based drug discovery
文献类型:会议论文
作者 | Ren, Jing; Li, Jian; Shi, Feng; Wang, Xin![]() ![]() ![]() ![]() |
出版日期 | 2013-01 |
卷号 | 48 |
期号 | 1 |
页码 | 14-24 |
英文摘要 | As an extension of the structure-based drug discovery, fragment-based drug discovery is matured increasingly, and plays an important role in drug development. Fragments in a small library, with lower molecular mass and high "ligand efficiency", are detected by SPR, MS, NMR, X-ray crystallography technologies and other biophysical methods. Then they are considered as starting points for chemical optimization with the guidance of structural biology methods to get good "drug-like" lead and candidate compounds. In this article, we reviewed the current progress of fragment-based drug discovery and detailed a number of examples to illustrate the novel strategies. |
会议录 | Yao xue xue bao = Acta pharmaceutica Sinica
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文献子类 | Meeting Abstract;Article;Review |
语种 | 中文 |
源URL | [http://119.78.100.183/handle/2S10ELR8/266883] ![]() |
专题 | 中国科学院上海药物研究所 |
作者单位 | State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China |
推荐引用方式 GB/T 7714 | Ren, Jing,Li, Jian,Shi, Feng,et al. Progress in the fragment-based drug discovery[C]. 见:. |
入库方式: OAI收割
来源:上海药物研究所
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