Literature DB >> 29924535

[Design, synthesis and evaluation of 4-pyridinylthiazole-2-amines as acetylcholinesterase inhibitors].

Ting-ting Cao, Jun-tao Chen, Chun-liu Yang, Yun-feng Tian, Teng-lei Feng, Zheng-yue Ma.   

Abstract

Alzheimer’s disease (AD) is a degenerative disease of the nervous system. Compound I reported to have inhibitory activity on AChE was used as a lead compound in this study, and 4-pyridinylthiazole-2-amines were designed by optimizing compound I structure. The new compounds were synthesized from acetylpyridines through five-steps of reaction, and their inhibition activities on AChE were measured in vitro by Ellman method. The new compounds exhibited a clear inhibitory activity on AChE in vitro. The bioactivity of compound 13c was the best among them, and its IC(50) value was 0.15 μmol·L(-1), which was better than that of rivastigmine and compound I in the control. Meanwhile, it exhibited little inhibition on butyrylcholinesterase. So the selective inhibitory activities of 4-pyridinylthiazole-2-amines to acetylcholinesterase were worth of studying furtherly.

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Year:  2016        PMID: 29924535

Source DB:  PubMed          Journal:  Yao Xue Xue Bao        ISSN: 0513-4870


  2 in total

1.  The Design, Synthesis and Evaluation of Rho-kinase Inhibitory Activity of 4-aryl-thiazole-2-amines.

Authors:  Linan Wang; Ben Ouyang; Meixia Fan; Junhui Qi; Lei Yao
Journal:  Iran J Pharm Res       Date:  2021       Impact factor: 1.696

2.  4-(Pyridin-4-yl)thiazol-2-amine as an efficient non-toxic inhibitor for mild steel in hydrochloric acid solutions.

Authors:  Xifeng Yang; Feng Li; Weiwei Zhang
Journal:  RSC Adv       Date:  2019-04-03       Impact factor: 4.036

  2 in total

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