A Green Method for Synthesis of 7H-thiazolo[3,2-b][1,2,4]-triazin-7-one Derivatives as AChE Inhibitors

被引:0
|
作者
Liu, Sijie [1 ]
Zhang, Baohua [1 ]
Jia, Pengfei [1 ]
Niu, Nan [1 ]
He, Jingyu [1 ]
Shi, Lanxiang [1 ]
机构
[1] Shijiazhuang Univ, Coll Chem Engn, Shijiazhuang, Hebei, Peoples R China
关键词
7H-thiazolo[3,2-b][1,2,4]triazin-7-ones; ionic liquid; AChE inhibitor; synthesize; ACETYLCHOLINESTERASE INHIBITORS; BIOLOGICAL EVALUATION; ALZHEIMERS-DISEASE; DESIGN;
D O I
10.1051/matecconf/20152502002
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
The authors study an efficient and green approach for the synthesis of 7H-thiazolo [3, 2-b][1,2,4]triazin-7-one derivatives as AChE inhibitors. The 7H-thiazolo[3,2-b][1,2,4]triazin-7-ones were designed by molecular docking, and readily prepared via a one-pot reaction in morpholine hydrosulfate ([Hnhm]HSO4) ionic liquid as the catalyst and solvent. The study of AChE inhibitory activity was carried out through using the Ellman colorimetric assay. The 7H-thiazolo[3,2-b][1,2,4]triazin-7-ones had been successfully synthesized by green catalyst. Most of the target compounds exhibited more than 50% inhibition at 10 mu M.
引用
收藏
页数:6
相关论文
共 50 条
  • [1] Design, Synthesis, and Biological Evaluation of 7H-thiazolo[3,2-b]-1,2,4-triazin-7-one Derivatives as Acetylcholinesterase Inhibitors
    Liu, Si-Jie
    Yang, Liu
    Liu, Xiao-Guang
    Luo, Ying
    Cao, Zi-Jian
    Wan, David Chi Cheong
    Lin, Huang-Quan
    Hu, Chun
    LETTERS IN DRUG DESIGN & DISCOVERY, 2010, 7 (01) : 5 - 8
  • [2] A green method for synthesis of 7H-thiazolo[3,2-b][1,2,4]triazin-7-one derivatives catalyzed by N-methylpyrrolidone hydrosulfate ([Hnmp]HSO4) ionic liquid
    Sijie Liu
    Lanxiang Shi
    Jingyu He
    Hongkun Yue
    Ran Zhou
    Monatshefte für Chemie - Chemical Monthly, 2014, 145 : 217 - 221
  • [3] An efficient electrochemical method for a unique synthesis of new derivatives of 7H-thiazolo[3,2-b]-1,2,4-triazin-7-one
    Fotouhi, L
    Nematollahi, D
    Heravi, MM
    Tammari, E
    TETRAHEDRON LETTERS, 2006, 47 (11) : 1713 - 1716
  • [4] A green method for synthesis of 7H-thiazolo[3,2-b][1,2,4]triazin-7-one derivatives catalyzed by N-methylpyrrolidone hydrosulfate ([Hnmp]HSO4) ionic liquid
    Liu, Sijie
    Shi, Lanxiang
    He, Jingyu
    Yue, Hongkun
    Zhou, Ran
    MONATSHEFTE FUR CHEMIE, 2014, 145 (01): : 217 - 221
  • [5] Synthesis and biological evaluation of 3,6-diaryl-7H-thiazolo[3,2-b] [1,2,4]triazin-7-one derivatives as acetylcholinesterase inhibitors
    Zhe Jin
    Liu Yang
    Si-Jie Liu
    Jian Wang
    Shuo Li
    Huang-Quan Lin
    David Chi Cheong Wan
    Chun Hu
    Archives of Pharmacal Research, 2010, 33 : 1641 - 1649
  • [6] Design, synthesis, and biological evaluation of 7H-thiazolo[3,2-b]-1,2,4-triazin-7-one derivatives as novel acetylcholinesterase inhibitors
    Liu, Si-jie
    Yang, Liu
    Jin, Zhe
    Huang, Er-fang
    Wan, David Chi Cheong
    Lin, Huang-quan
    Hu, Chun
    ARKIVOC, 2009, : 333 - 348
  • [7] Design, synthesis and antibacterial activity of novel 7H-thiazolo [3,2-b]-1,2,4-triazin-7-one derivatives
    Hou, Shicheng
    Li, Tai
    Yan, Jiangqing
    Cai, Dong
    Peng, Yang
    Zhang, Haibo
    Tong, Feng
    Fan, Haiming
    Liu, Xiaoping
    Hu, Chun
    HELIYON, 2024, 10 (03)
  • [8] Synthesis and Biological Evaluation of 3,6-diaryl-7H-thiazolo[3,2-b] [1,2,4]triazin-7-one Derivatives as Acetylcholinesterase Inhibitors
    Jin, Zhe
    Yang, Liu
    Liu, Si-Jie
    Wang, Jian
    Li, Shuo
    Lin, Huang-Quan
    Wan, David Chi Cheong
    Hu, Chun
    ARCHIVES OF PHARMACAL RESEARCH, 2010, 33 (10) : 1641 - 1649
  • [9] Synthesis and biological activity of 3,6-diaryl-7H-thiazolo[3,2-b][1,2,4]triazin-7-one derivatives as novel acetylcholinesterase inhibitors
    WAN David ChiCheong
    Science China(Chemistry), 2010, 53 (11) : 2297 - 2303
  • [10] Synthesis and biological activity of 3,6-diaryl-7H-thiazolo[3,2-b] [1,2,4]triazin-7-one derivatives as novel acetylcholinesterase inhibitors
    Jin Zhe
    Yang Liu
    Xu HeNan
    Huang ErFang
    Wan David ChiCheong
    Li Shuo
    Lin HuangQuan
    Hu Chun
    SCIENCE CHINA-CHEMISTRY, 2010, 53 (11) : 2297 - 2303