鉴定(生物学)
化学空间
药物发现
被忽视的热带疾病
生化工程
纳米技术
风险分析(工程)
化学
数据科学
计算生物学
管理科学
计算机科学
工程类
医学
疾病
生物
材料科学
生态学
生物化学
病理
作者
Rafael V. C. Guido,Glaucius Oliva,Adriano D. Andricopulo
标识
DOI:10.1351/pac-con-11-11-07
摘要
Drug discovery has moved toward more rational strategies based on our increasing understanding of the fundamental principles of protein–ligand interactions. Structure- (SBDD) and ligand-based drug design (LBDD) approaches bring together the most powerful concepts in modern chemistry and biology, linking medicinal chemistry with structural biology. The definition and assessment of both chemical and biological space have revitalized the importance of exploring the intrinsic complementary nature of experimental and computational methods in drug design. Major challenges in this field include the identification of promising hits and the development of high-quality leads for further development into clinical candidates. It becomes particularly important in the case of neglected tropical diseases (NTDs) that affect disproportionately poor people living in rural and remote regions worldwide, and for which there is an insufficient number of new chemical entities being evaluated owing to the lack of innovation and R&D investment by the pharmaceutical industry. This perspective paper outlines the utility and applications of SBDD and LBDD approaches for the identification and design of new small-molecule agents for NTDs.
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