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Structure- and ligand-based drug design approaches for neglected tropical diseases*

机译:基于结构和配体的忽视热带疾病的药物设计方法*

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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.
机译:根据我们越来越多地了解蛋白质 - 配体相互作用的基本原则,药物发现已经朝着更合理的策略迁移。结构 - (SBDD)和基于配体的药物设计(LBDD)方法将在现代化学和生物学中提出最强大的概念,将药物化学与结构生物学联系起来。化学和生物空间的定义和评估恢复了探索药物设计中实验和计算方法的内在互补性的重要性。该领域的主要挑战包括识别有前途的命中和高质量领导的发展,以进一步发展临床候选者。在忽视的热带疾病(NTDS)的情况下尤为重要,这些热带疾病(NTDS)影响居住在全世界农村和偏远地区的贫困人口,而且由于缺乏创新和研发投资而被评估的新化学实体数量不足由制药行业。该透视论文概述了SBDD和LBDD方法的鉴定和设计NTDS新的小分子试剂的效用和应用。

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