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NaClO-Mediated Cross Installation of Indoles and Azoles Benefits Anticancer Hit Discovery.

Changjun YuRuiyao EXiao-Wei ZhangWen-Qian HuGuangjun BaoYiping LiYuyang LiuZeyuan HeJingyue LiWen MaLing-Yun MouRui WangWangsheng Sun
Published in: ChemMedChem (2023)
Innovations in synthetic chemistry have a profound impact on the drug discovery process, and will always be a necessary driver of drug development. As a result, it is of significance to develop novel simple and effective synthetic installation of medicinal modules to promote drug discovery. Herein, we have developed a NaClO-mediated cross installation of indoles and azoles, both of which are frequently encountered in drugs and natural products. This effective toolbox provides a convenient synthetic route to access a library of N-linked 2-(azol-1-yl) indole derivatives, and can be used for late-stage modification of drugs, natural products and peptides. Moreover, biological screening of the library has revealed that several adducts showed promising anticancer activities against A549 and NCI-H1975 cells, which give us a hit for anticancer drug discovery.
Keyphrases
  • drug discovery
  • induced apoptosis
  • small molecule
  • cell cycle arrest
  • high throughput
  • signaling pathway
  • drug induced
  • endoplasmic reticulum stress
  • amino acid
  • network analysis