2-Styryl-4-aminoquinazoline derivatives as potent DNA-cleavage, p53-activation and in vivo effective anticancer agents-Reference-Cited by-同舟云学术

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2-Styryl-4-aminoquinazoline derivatives as potent DNA-cleavage, p53-activation and in vivo effective anticancer agents

Published:2020-01 Issue: Volume:186 Page:111851
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Wei Xin-Wei,Yuan Jing-Mei,Huang Wan-Yun,Chen Nan-Ying,Li Xiao-Juan,Pan Cheng-Xue^ORCID,Mo Dong-Liang,Su Gui-Fa^ORCID

Funder

National Natural Science Foundation of China

Guangxi Natural Science Foundation

Foundation of State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources

Guangxi Normal University

Innovation Project of Guangxi Graduate Education

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference39 articles.

1. Small molecules inhibit STAT3 activation, autophagy, and cancer cell anchorage-independent growth;Zhou;Bioorg. Med. Chem.,2017

2. The p53 stabilizing agent CP-31398 and multi-kinase inhibitors. Designing, synthesizing and screening of styrylquinazoline series;Mularski;Eur. J. Med. Chem.,2019

3. Synthesis and biological evaluation of novel quinazoline-4-piperidine sulfamide derivatives as inhibitors of NPP1;Forcellini;Eur. J. Med. Chem.,2018

4. Structure-based target specific screening leads to small-molecule CaMKII inhibitors;Xu;ChemMedChem,2017

5. Therapeutic reactivation of mutant p53 protein by quinazoline derivatives;Sutherland;Investig. New Drugs,2012

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