Biological Evaluation of Some Uracil Derivatives as Potent Glutathione Reductase Inhibitors

被引:1
|
作者
Guney, Murat [1 ]
Ekinci, Deniz [2 ]
Cavdar, Huseyin [3 ]
Senturk, Murat [1 ]
Zilbeyaz, Kani [1 ]
机构
[1] Ibrahim Cecen Univ Agri, Sci & Art Fac, Dept Chem, Agri, Turkey
[2] Ondokuz Mayis Univ, Fac Agr, Agr Biotechnol Dept, Samsun, Turkey
[3] Dumlupinar Univ, Fac Educ, Kutahya, Turkey
关键词
IN-VITRO; DESIGN;
D O I
10.1063/1.4945930
中图分类号
O59 [应用物理学];
学科分类号
摘要
Discovery of glutathione reductase (GR) inhibitors has become very popular recently due to antimalarial and anticancer activities. In this study, GR inhibitory capacities of some uracil derivatives (UDCs) (1-4) were reported. Some commercially available molecules (5-6) were also tested for comparison reasons. The novel UDCs were obtained in high yields using simple chemical procedures and exhibited much potent inhibitory activities against GR at low nanomolar concentrations with IC50 values ranging from 2.68 to 166.6 nM as compared with well-known agents.
引用
收藏
页数:3
相关论文
共 50 条
  • [21] Design, synthesis, and biological evaluation of tetrahydroquinolin derivatives as potent inhibitors of CBP bromodomain
    Chen, Yu
    Bi, Xiaoyang
    Zhang, Fengcai
    Sun, Zhongya
    Xu, Pan
    Jiang, Hao
    Lu, Wenchao
    Lu, Tian
    Ding, Hong
    Zhang, Naixia
    Jiang, Hualiang
    Chen, Kaixian
    Zhou, Bing
    Luo, Cheng
    BIOORGANIC CHEMISTRY, 2020, 101
  • [22] Design, Synthesis, and Biological Evaluation of Novel Acylhydrazone Derivatives as Potent Neuraminidase Inhibitors
    Li, Meng
    Cheng, Li Ping
    Pang, Wan
    Zhong, Zhi Jian
    Guo, Ling Ling
    ACS MEDICINAL CHEMISTRY LETTERS, 2020, 11 (09): : 1745 - 1750
  • [23] Synthesis, molecular docking, and biological evaluation of nitroimidazole derivatives as potent urease inhibitors
    Meysam Talebi
    Elham Hamidian
    Fatemeh Niasari-Naslaji
    Sogand Rahmani
    Faezeh Sadat Hosseini
    Shahin Boumi
    Mohammad Nazari Montazer
    Mehdi Asadi
    Massoud Amanlou
    Medicinal Chemistry Research, 2021, 30 : 1220 - 1229
  • [24] Design, synthesis and biological evaluation of novel thiazole derivatives as potent FabH inhibitors
    Lv, Peng-Cheng
    Wang, Kai-Rui
    Yang, Ying
    Mao, Wen-Jun
    Chen, Jin
    Xiong, Jing
    Zhu, Hai-Liang
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2009, 19 (23) : 6750 - 6754
  • [25] Synthesis and biological evaluation of benzyl styrylsulfonyl derivatives as potent anticancer mitotic inhibitors
    Chahrour, Osama
    Abdalla, Ashraf
    Lam, Frankie
    Midgley, Carol
    Wang, Shudong
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2011, 21 (10) : 3066 - 3069
  • [26] Design, synthesis and biological evaluation of spiropyrazolopyridone derivatives as potent dengue virus inhibitors
    Xu, Jimin
    Xie, Xuping
    Chen, Haiying
    Zou, Jing
    Xue, Yu
    Ye, Na
    Shi, Pei-Yong
    Zhou, Jia
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2020, 30 (11)
  • [27] Design, synthesis and biological evaluation of novel zanamivir derivatives as potent neuraminidase inhibitors
    Cheng, Li Ping
    Wang, Tian Chi
    Yu, Rao
    Li, Meng
    Huang, Jin Wen
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2018, 28 (23-24) : 3622 - 3629
  • [28] Synthesis and biological evaluation of triazole based uracil derivatives as novel DPP-4 inhibitors
    Li, Qing
    Han, Li
    Zhang, Bin
    Zhou, Jinpei
    Zhang, Huibin
    ORGANIC & BIOMOLECULAR CHEMISTRY, 2016, 14 (40) : 9598 - 9611
  • [29] An Efficient Synthesis of Quinoxalinone Derivatives as Potent Inhibitors of Aldose Reductase
    Yang, Yanchun
    Zhang, Shuzhen
    Wu, Bobin
    Ma, Mingming
    Chen, Xin
    Qin, Xiangyu
    He, Minlan
    Hussain, Saghir
    Jing, Chaojun
    Ma, Bing
    Zhu, Changjin
    CHEMMEDCHEM, 2012, 7 (05) : 823 - 835
  • [30] Synthesis and Biological Evaluation of Atorvastatin Derivatives as Novel HMG-CoA Reductase Inhibitors
    Tong, Jiayi
    Wang, Naxin
    Xiao, Hua
    LETTERS IN DRUG DESIGN & DISCOVERY, 2013, 10 (09) : 817 - 822