DOI: 10.1039/d6ra09088e ISSN: 2046-2069

Design, click synthesis, and biological evaluation of novel uracil-1,2,3-triazole hybrids as dual EGFR/CDK1 inhibitors: antiproliferative activity, mechanistic insights, and in silico studies

Asmaa H. Mohamed, Ashraf A. Aly, Elshimaa M. N. Abdelhafez, Aya A. Fouly, Alan B. Brown, Sageda A. Gedamy

A novel series of uracil–1,2,3-triazole hybrids was designed, synthesized, and evaluated as dual EGFR/CDK1 inhibitors to target cancer cell proliferation and survival.

More from our Archive