Nornostocine congeners as potential anticancer drugs: An overview

被引:13
|
作者
Sahoo, Chita R. [1 ,2 ,3 ]
Paidesetty, Sudhir K. [3 ]
Padhy, Rabindra N. [1 ,2 ]
机构
[1] Siksha O Anusandhan Deemed Be Univ, Inst Med Sci, Cent Res Lab, Bhubaneswar 751003, Odisha, India
[2] Siksha O Anusandhan Deemed Be Univ, Sum Hosp, Bhubaneswar 751003, Odisha, India
[3] Siksha O Anusandhan Deemed Be Univ, Sch Pharmaceut Sci, Dept Med Chem, Bhubaneswar 751003, Odisha, India
关键词
antiproliferation; cyanobacteria; pyrazolo[4; 3-e][1; 2; 4] triazole; SAR; SILDENAFIL ANALOGS; NOSTOCINE-A; SULFONAMIDES; TYROSINASE;
D O I
10.1002/ddr.21577
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The naturally occurring phyco-constituent nostocine A, bearing the pyrazolotriazine scaffold in its structural frame, belongs to an organic class of pharmacologically curious candidates with a remarkable anticancer activity. This review summarizes the chemistry of numerous synthetic strategies of demethylated nostocine as "nornostocine derivatives," in which the substitutes are connected to a few functionalities with the pyrazolotriazine moiety at N-1, C-3, and C-5 positions. These strategies may provide a framework to design and develop a novel potent anticancer drug candidate(s) with an augment of structure activity relationship related to anticancer activities.
引用
收藏
页码:878 / 892
页数:15
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