Design and Synthesis of a Novel Covalent Dihydropteridinone Derivative as a Highly Potent and Orally Bioavailable PLK1 Inhibitor for the Treatment of Chronic Myeloid Leukemia
- DOI
- 10.1021/acs.jmedchem.6c01512
- Published
- 2026-06-30
- Container
- Journal of Medicinal Chemistry
- Publisher
- American Chemical Society (ACS)
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1021/acs.jmedchem.6c01512,
title = {Design and
Synthesis of a Novel Covalent Dihydropteridinone
Derivative as a Highly Potent and Orally Bioavailable PLK1 Inhibitor
for the Treatment of Chronic Myeloid Leukemia},
author = {Jiaxu Zhou and Zhongtang Li and Xiaojiao Sun and Xiangyu Zhang and Yan He and Cheng Shi and Xiaowei Chi and Dehua Lu and Weiping Lyu and Siyu Xiu and Tingting Yang and Yanming Chen and Zhongwei Wang and Qi Li and Ruqiu Zheng and Jiarui Du and Yu Lin and Jinghao Yan and Tengfei Li and Chenzhong Liao and Liangren Zhang and Zhenming Liu},
year = {2026},
journal = {Journal of Medicinal Chemistry},
doi = {10.1021/acs.jmedchem.6c01512},
url = {https://doi.org/10.1021/acs.jmedchem.6c01512}
}RIS
TY - JOUR TI - Design and Synthesis of a Novel Covalent Dihydropteridinone Derivative as a Highly Potent and Orally Bioavailable PLK1 Inhibitor for the Treatment of Chronic Myeloid Leukemia AU - Jiaxu Zhou AU - Zhongtang Li AU - Xiaojiao Sun AU - Xiangyu Zhang AU - Yan He AU - Cheng Shi AU - Xiaowei Chi AU - Dehua Lu AU - Weiping Lyu AU - Siyu Xiu AU - Tingting Yang AU - Yanming Chen AU - Zhongwei Wang AU - Qi Li AU - Ruqiu Zheng AU - Jiarui Du AU - Yu Lin AU - Jinghao Yan AU - Tengfei Li AU - Chenzhong Liao AU - Liangren Zhang AU - Zhenming Liu PY - 2026 JO - Journal of Medicinal Chemistry DO - 10.1021/acs.jmedchem.6c01512 UR - https://doi.org/10.1021/acs.jmedchem.6c01512 ER -
APA
Zhou, J., Li, Z., Sun, X., Zhang, X., He, Y., Shi, C., Chi, X., Lu, D., Lyu, W., Xiu, S., Yang, T., Chen, Y., Wang, Z., Li, Q., Zheng, R., Du, J., Lin, Y., Yan, J., Li, T., Liao, C., Zhang, L., & Liu, Z. (2026). Design and Synthesis of a Novel Covalent Dihydropteridinone Derivative as a Highly Potent and Orally Bioavailable PLK1 Inhibitor for the Treatment of Chronic Myeloid Leukemia. Journal of Medicinal Chemistry. https://doi.org/10.1021/acs.jmedchem.6c01512
Source records
- crossref · retrieved 2026-09-26T13:02:23.459Z