Design, synthesis and biological evaluation of 4-(indolin-1-yl)-6-substituted-pyrido[3,2-d]pyrimidine derivatives as Mnk1/2 inhibitors-Reference-Cited by-同舟云学术

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Design, synthesis and biological evaluation of 4-(indolin-1-yl)-6-substituted-pyrido[3,2-d]pyrimidine derivatives as Mnk1/2 inhibitors

Published:2024-06 Issue: Volume:272 Page:116499
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Xing Kun,Zhang Huimin,Wang Shuxiang,Li Jinghuan,Mu Zhiying,Zhang Lanxin,Zuo Shuwei,Wang Yuetong,Li Shujun,Wu Boyang,Jing Yongkui,Wen Jiachen,Liu Dan,Huang Min,Zhao Linxiang

Funder

National Natural Science Foundation of China

Liaoning Revitalization Talents Program

Publisher

Elsevier BV

Reference22 articles.

1. MAP kinase-interacting kinases–emerging targets against cancer;Diab;Chem. Biol.,2014

2. Biological functions and research progress of eIF4E;Chen;Front. Oncol.,2023

3. Mitogen-activated protein kinase (MAPK) interacting kinases 1 and 2 (MNK1 and MNK2) as targets for cancer therapy: Recent progress in the development of MNK inhibitors;Dreas;Curr. Med. Chem.,2017

4. Deeping in the role of the MAP-kinases interacting kinases (MNKs) in cancer;Pinto-Díez;Int. J. Mol. Sci.,2020

5. Update on the development of MNK inhibitors as therapeutic agents;Xu;J. Med. Chem.,2022

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