Review of the Synthesis and Anticancer Properties of Pyrazolo[4,3-e][1,2,4]triazine Derivatives

被引：26
|
作者：
Bernat, Zofia [1 ]
Szymanowska, Anna [2 ]
Kciuk, Mateusz [3 ,4 ]
Kotwica-Mojzych, Katarzyna [5 ]
Mojzych, Mariusz [1 ]
机构：
[1] Siedlce Univ Nat Sci & Humanities, Dept Chem, 3 Maja 54, PL-08110 Siedlce, Poland
[2] Med Univ Bialystok, Dept Biotechnol, Kilinskiego 1, PL-15222 Bialystok, Poland
[3] Univ Lodz, Dept Mol Biotechnol & Genet, Lab Cytogenet, Banacha 12-16, PL-90237 Lodz, Poland
[4] Univ Lodz, Doctoral Sch Exact & Nat Sci, Banacha St 12-16, PL-90237 Lodz, Poland
[5] Med Univ Lublin, Coll Med, Dept Histol Embryol & Cytophysiol, Radziwillowska 11, PL-20080 Lublin, Poland
来源：
MOLECULES | 2020年 / 25卷 / 17期
关键词：
pyrazolo[4; 3-e][1; 2; 4]triazines; anticancer activity; sulfonamides; 1; 4-triazine; fused tetrazole derivatives; fluviols; CARBONIC-ANHYDRASE INHIBITORS; ORGANIC-SYNTHESIS; PROTEIN; 1,2,4-TRIAZINES; FAMILY; PHENYLHYDRAZONES; SULFONAMIDES; NOSTOCINE; TARGETS; CLONING;
D O I：
10.3390/molecules25173948
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：
This review focuses on the cytotoxic effect of new synthetic pyrazolo[4,3-e][1,2,4]triazine derivatives against different tumor cell lines. Some annulated pyrazolotriazines i.e., pyrazolo[4,3-e][1,2,4]triazolo[4,3-b][1,2,4]triazines and pyrazolo[4,3-e]tetrazolo[1,5-b][1,2,4]triazine demonstrated significant broad cytotoxic activity in micromolar range concentration, which could have excellent potential to be new candidate therapeutic agents in cancer chemotherapy.
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收藏
页数：20
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