Design, synthesis and biological evaluation of novel perimidine o-quinone derivatives as non-intercalative topoisomerase II catalytic inhibitors-Reference-Cited by-同舟云学术

Design, synthesis and biological evaluation of novel perimidine o-quinone derivatives as non-intercalative topoisomerase II catalytic inhibitors

Published:2019-10 Issue: Volume:91 Page:103131
ISSN:0045-2068
Container-title:Bioorganic Chemistry
language:en
Short-container-title:Bioorganic Chemistry

Author:

Zhou Du-Chao,Lu Yu-Ting,Mai Yan-Wen,Zhang Chen,Xia Jie,Yao Pei-Fen,Wang Hong-Gen,Huang Shi-Liang,Huang Zhi-Shu

Funder

Guangdong Provincial Key Laboratory of Construction Foundation

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Molecular Biology,Biochemistry

Reference22 articles.

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4. Activity of topoisomerase inhibitors daunorubicin, idarubicin, and aclarubicin in the Drosophila Somatic Mutation and Recombination Test;Lehmann;Environ. Mol. Mutagen.,2004

5. Selection of human leukemic CEM cells for resistance to the DNA topoisomerase II catalytic inhibitor ICRF-187 results in increased levels of topoisomerase IIalpha and altered G(2)/M checkpoint and apoptotic responses;Morgan;Mol. Pharmacol.,2000

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