Focused Combinatorial Library Design Based on Structural Diversity, Druglikeness and Binding Affinity Score-Reference-Cited by-同舟云学术

Focused Combinatorial Library Design Based on Structural Diversity, Druglikeness and Binding Affinity Score

Published:2005-03-18 Issue:3 Volume:7 Page:398-406
ISSN:1520-4766
Container-title:Journal of Combinatorial Chemistry
language:en
Short-container-title:J. Comb. Chem.

Author:

Chen Gang¹,Zheng Suxin¹,Luo Xiaomin¹,Shen Jianhua¹,Zhu Weiliang¹,Liu Hong¹,Gui Chunshan¹,Zhang Jian¹,Zheng Mingyue¹,Puah Chum Mok¹,Chen Kaixian¹,Jiang Hualiang¹

Affiliation:

1. Drug Discovery and Design Center and State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Shanghai Institutes for Biological Sciences, and Graduate School, Chinese Academy of Sciences, 555 Zuchongzhi Road, Shanghai 201203, P. R. China, Technology Centre for Life Sciences, Singapore Polytechnic, 500 Dover Road, Singapore 139651, Singapore, School of Pharmacy, East China University of Science and Technology, Shanghai 200237, China

Publisher

American Chemical Society (ACS)

Subject

General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/cc049866h

Reference67 articles.

1. Applications of Combinatorial Technologies to Drug Discovery. 1. Background and Peptide Combinatorial Libraries

2. Applications of Combinatorial Technologies to Drug Discovery. 2. Combinatorial Organic Synthesis, Library Screening Strategies, and Future Directions

3. Combinatorial synthesis — the design of compound libraries and their application to drug discovery

4. Serendipity meets precision: the integration of structure-based drug design and combinatorial chemistry for efficient drug discovery

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