Design, synthesis and biological evaluation of quinazoline-based covalent PI3Kδ inhibitors targeting Lys779 residue.
- DOI
- 10.1016/j.bioorg.2026.110695
- Published
- 2026 Oct 26
- Container
- Bioorganic chemistry
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1016/j.bioorg.2026.110695,
title = {Design, synthesis and biological evaluation of quinazoline-based covalent PI3Kδ inhibitors targeting Lys779 residue.},
author = {Ma N and Feng Y and Yuan B and Wei Z and Lai Y and Chen M and Tang Y and Wang J and Xin M},
year = {2026},
journal = {Bioorganic chemistry},
doi = {10.1016/j.bioorg.2026.110695},
url = {https://doi.org/10.1016/j.bioorg.2026.110695}
}RIS
TY - JOUR TI - Design, synthesis and biological evaluation of quinazoline-based covalent PI3Kδ inhibitors targeting Lys779 residue. AU - Ma N AU - Feng Y AU - Yuan B AU - Wei Z AU - Lai Y AU - Chen M AU - Tang Y AU - Wang J AU - Xin M PY - 2026 JO - Bioorganic chemistry DO - 10.1016/j.bioorg.2026.110695 UR - https://doi.org/10.1016/j.bioorg.2026.110695 ER -
APA
N, M., Y, F., B, Y., Z, W., Y, L., M, C., Y, T., J, W., & M, X. (2026). Design, synthesis and biological evaluation of quinazoline-based covalent PI3Kδ inhibitors targeting Lys779 residue.. Bioorganic chemistry. https://doi.org/10.1016/j.bioorg.2026.110695
Source records
- pubmed · retrieved 2026-11-10T11:24:04.315Z