Design of novel uracil derivatives as inhibitors of carbonic anhydrases I & II, acetylcholinesterase, butyrylcholinesterase, and glutathione reductase using in silico, synthesis and in vitro studies

被引：0
|
作者：
Durdagi, S. [1 ]
Senturk, M. [2 ]
Guney, M. [2 ]
Ekinci, D. [3 ]
Aksoydan, B. [1 ]
Erol, I. [1 ]
Kantarcioglu, I. [1 ]
Cavdar, H. [4 ]
机构：
[1] Bahcesehir Univ, Sch Med, Dept Biophys, Istanbul, Turkey
[2] Ibrahim Cecen Univ Agri, Dept Chem, Agri, Turkey
[3] Ondokuz Mayis Univ, Dept Agr Biotechnol, Samsun, Turkey
[4] Dumlupinar Univ, Fac Educ, Kutahya, Turkey
来源：
FEBS JOURNAL | 2016年 / 283卷
关键词：
D O I：
暂无
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：
ST03022005
引用
收藏
页码：106 / 106
页数：1
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