De novo design of inhibitors of DNA methyltransferase 1: A critical comparison of ligand- and structure-based approaches

Diana L. Prado-Romero,Fernanda I. Saldívar-González, Iván López-Mata, Pedro A. Laurel-García,Norberto Sánchez-Cruz,José L. Medina-Franco

crossref(2024)

引用 0|浏览0
暂无评分
摘要
Designing and developing inhibitors against the epigenetic target DNA methyltransferase (DNMT) is an attractive strategy in epigenetic drug discovery. DNMT1 is one of the epigenetic enzymes with significant clinical relevance. Structure-based de novo design is a drug discovery strategy used in combination with similarity searching to identify a novel DNMT inhibitor with a novel chemical scaffold and warrants further exploration. This study aimed to continue exploring the potential of de novo design to build epigenetic-focused libraries targeted toward DNMT1. Herein, we report the results of an in-depth and critical comparison of ligand- and structure-based de novo design of screening libraries focused on DNMT1. The newly designed chemical libraries focused on DNMT1 are freely available on GitHub at https://github.com/DIFACQUIM/De-Novo_DNMT1.
更多
查看译文
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要