1,3,5-Triazines: A promising scaffold for anticancer drugs development

被引:118
|
作者
Cascioferro, Stella [1 ]
Parrino, Barbara [1 ]
Spano, Virginia [1 ]
Carbone, Anna [1 ]
Montalbano, Alessandra [1 ]
Barraja, Paola [1 ]
Diana, Patrizia [1 ]
Cirrincione, Girolamo [1 ]
机构
[1] Univ Palermo, Dipartimento Sci & Tecnol Biol Chim & Farmaceut S, Via Archirafi 32, I-90123 Palermo, Italy
关键词
1,3,5-Triazines; Antitumor activity; Nitrogen heterocycles; Disubstituted 1,3,5-triazines; Trisubstituted 1,3,5-triazines; Heterofused 1,3,5-triazines; CARBONIC-ANHYDRASE INHIBITORS; COMPETITIVE MTOR INHIBITORS; STRUCTURE-BASED DESIGN; BREAST-CANCER CELLS; IN-VITRO EVALUATION; THYMIDINE PHOSPHORYLASE; ANTIPROLIFERATIVE ACTIVITY; BIOLOGICAL EVALUATION; KINASE INHIBITORS; ANTITUMOR EVALUATION;
D O I
10.1016/j.ejmech.2017.09.035
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
This review covering literature reports from the beginning of this century to 2016 describes the synthetic pathways, the antitumor activity, the structure-activity relationship and, whenever reported, the possible mechanism of action of 1,3,5-triazine derivatives as well as of their hetero-fused compounds. Many 1,3,5-triazine derivatives, both uncondensed and hetero-fused, have shown remarkable antitumor activities and some of them reached clinical development. (C) 2017 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:523 / 549
页数:27
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