Synthesis and Characterization of Novel Unsymmetrical and Symmetrical 3-Halo- or 3-Methoxy-substituted 2-Dibenzoylamino-1,4-naphthoquinone Derivatives

被引:13
作者
Brandy, Yakini [1 ]
Brandy, Nailah [1 ]
Akinboye, Emmanuel [1 ]
Lewis, Malik [1 ]
Mouamba, Claudia [1 ]
Mack, Seshat [1 ]
Butcher, Ray J. [1 ]
Anderson, Alan J. [2 ]
Bakare, Oladapo [1 ]
机构
[1] Howard Univ, Dept Chem, Washington, DC 20059 USA
[2] Bowie State Univ, Dept Nat Sci, Bowie, MD 20715 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
1,4-naphthoquinone; imide synthesis; sodium hydride-promoted bis-acylation; unsymmetrical imide; BIOLOGICAL EVALUATION; NAPHTHOQUINONE DERIVATIVES; HETEROCYCLIC QUINONES; CYTOTOXICITY; 2,3-DICHLORO-5,8-DIMETHOXY-1,4-NAPHTHOQUINONE; INHIBITORS; DISRUPTS; TUBULIN; DESIGN;
D O I
10.3390/molecules18021973
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Symmetrical and unsymmetrical 3-halo- or 3-methoxy- substituted 2-dibenzoylamino-1,4-naphthoquinone analogs were synthesized with an average yield of 45% via sodium hydride promoted bis-acylation of 2-amino-3-chloro-1,4-naphthoquinone, 2-amino-3-bromo-1,4-naphthoquinone and 2-amino-3-methoxy-1,4-naphthoquinone.
引用
收藏
页码:1973 / 1984
页数:12
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