Design, click synthesis, and biological evaluation of novel uracil-1,2,3-triazole hybrids as dual EGFR/CDK1 inhibitors: antiproliferative activity, mechanistic insights, and <i>in silico</i> studies.
- DOI
- 10.1039/d6ra09088e
- Published
- 2026-11-03
- Container
- RSC Adv
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1039/d6ra09088e,
title = {Design, click synthesis, and biological evaluation of novel uracil-1,2,3-triazole hybrids as dual EGFR/CDK1 inhibitors: antiproliferative activity, mechanistic insights, and \<i\>in silico\</i\> studies.},
author = {Mohamed AH and Aly AA and Abdelhafez EMN and Fouly AA and Brown AB and Gedamy SA.},
year = {2026},
journal = {RSC Adv},
doi = {10.1039/d6ra09088e},
url = {https://doi.org/10.1039/d6ra09088e}
}RIS
TY - JOUR TI - Design, click synthesis, and biological evaluation of novel uracil-1,2,3-triazole hybrids as dual EGFR/CDK1 inhibitors: antiproliferative activity, mechanistic insights, and <i>in silico</i> studies. AU - Mohamed AH AU - Aly AA AU - Abdelhafez EMN AU - Fouly AA AU - Brown AB AU - Gedamy SA. PY - 2026 JO - RSC Adv DO - 10.1039/d6ra09088e UR - https://doi.org/10.1039/d6ra09088e ER -
APA
AH, M., AA, A., EMN, A., AA, F., AB, B., & SA., G. (2026). Design, click synthesis, and biological evaluation of novel uracil-1,2,3-triazole hybrids as dual EGFR/CDK1 inhibitors: antiproliferative activity, mechanistic insights, and <i>in silico</i> studies.. RSC Adv. https://doi.org/10.1039/d6ra09088e
Source records
- europe-pmc · retrieved 2026-11-10T08:00:51.415Z