Design, synthesis and anti-tumor activity evaluation of 4,6,7-substitute quinazoline derivatives-Reference-Cited by-同舟云学术

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Design, synthesis and anti-tumor activity evaluation of 4,6,7-substitute quinazoline derivatives

Published:2022-06-06 Issue:8 Volume:31 Page:1351-1368
ISSN:1054-2523
Container-title:Medicinal Chemistry Research
language:en
Short-container-title:Med Chem Res

Author:

Dai Honglin,Si Xiaojie,Wang Hao,Chi Lingling,Gao Chao,Wang Zhengjie,Liu Limin,Qian Zhuo,Ke Yu,Zhang Qiurong,Liu Hongmin

Funder

National Natural Science Foundation of China

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,General Pharmacology, Toxicology and Pharmaceutics

Link

https://link.springer.com/content/pdf/10.1007/s00044-022-02897-9.pdf

Reference36 articles.

1. Akhtar J, Khan AA, Ali Z, Haider R, Shahar Yar M. Structure-activity relationship (SAR) study and design strategies of nitrogen-containing heterocyclic moieties for their anticancer activities. Eur J Med Chem. 2017;125:143–89. https://doi.org/10.1016/j.ejmech.2016.09.023

2. Elmetwally SA, Saied KF, Eissa IH, Elkaeed EB. Design, synthesis and anticancer evaluation of thieno[2,3-d]pyrimidine derivatives as dual EGFR/HER2 inhibitors and apoptosis inducers. Bioorg Chem. 2019;88:102944 https://doi.org/10.1016/j.bioorg.2019.102944

3. Fouad MM, El-Bendary ER, Suddek GM, Shehata IA, El-Kerdawy MM. Synthesis and in vitro antitumor evaluation of some new thiophenes and thieno[2,3-d]pyrimidine derivatives. Bioorg Chem. 2018;81:587–98. https://doi.org/10.1016/j.bioorg.2018.09.022

4. D’Alterio C, Scala S, Sozzi G, Roz L, Bertolini G. Paradoxical effects of chemotherapy on tumor relapse and metastasis promotion. Semin Cancer Biol. 2020;60:351–61. https://doi.org/10.1016/j.semcancer.2019.08.019

5. Bernchou U, Arnold TST, Axelsen B, Kluver-Kristensen M, Mahmood F, Harbo FSG, et al. Evolution of the gross tumour volume extent during radiotherapy for glioblastomas. Radiother Oncol. 2021;160:40–6. https://doi.org/10.1016/j.radonc.2021.04.001

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