嘧啶
吡啶
癌症
组合化学
化学
小分子
药物发现
药理学
计算生物学
医学
生物
生物化学
有机化学
内科学
作者
Supaluk Prachayasittikul,Ratchanok Pingaew,Apilak Worachartcheewan,Nujarin Sinthupoom,Veda Prachayasittikul,Somsak Ruchirawat,Virapong Prachayasittikul
标识
DOI:10.2174/1389557516666160923125801
摘要
Cancer has been considered to be a global health concern due to the impact of disease on the quality of life. The continual increase of cancer cases as well as the resistance of cancer cells to the existing drugs have driven the search for novel anticancer drugs with better potency and selectivity, improved pharmacokinetic profiles, and minimum toxicities. Pyridine and pyrimidine are presented in natural products and genetic materials. These pyridine/pyrimidine core structures have been noted for their roles in many biological processes as well as in cancer pathogenesis, which make such compounds become attractive scaffolds for discovery of novel drugs.In the recent years, pyridine- and pyrimidine-based anticancer drugs have been developed based on structural modification of these core structures (i.e., substitution with moieties and rings, conjugation with other compounds, and coordination with metal ions). Detailed discussion is provided in this review to highlight the potential of these small molecules as privileged scaffolds with attractive properties and biological activities for the search of novel anticancer agents.
科研通智能强力驱动
Strongly Powered by AbleSci AI