Synthesis and DNA-sequence selectivity of a series of mono- and difunctional 9-aminoacridine nitrogen mustards
Author:
Publisher
American Chemical Society (ACS)
Subject
Drug Discovery,Molecular Medicine
Link
https://pubs.acs.org/doi/pdf/10.1021/jm00027a008
Cited by 26 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Therapeutic journery of nitrogen mustard as alkylating anticancer agents: Historic to future perspectives;European Journal of Medicinal Chemistry;2018-05
2. Synthesis, characterization and antitumor activity of 2-methyl-9-substituted acridines;Arabian Journal of Chemistry;2017-02
3. ChemInform Abstract: Synthesis and DNA-Sequence Selectivity of a Series of Mono- and Difunctional 9-Aminoacridine Nitrogen Mustards.;ChemInform;2010-08-19
4. DNA-targeting pyrroloquinoline-linked butenone and chalcones: Synthesis and biological evaluation;European Journal of Medicinal Chemistry;2009-07
5. Synthesis and in vitro cytotoxicity of 9-anilinoacridines bearing N-mustard residue on both anilino and acridine rings;European Journal of Medicinal Chemistry;2009-07
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