scholarly journals Synthesis and Biological Evaluation of Novel Glycosyl-Containing 1,2,4-Triazolo[3,4-b][1,3,4]Thiadiazole Derivatives as Acetylcholinesterase Inhibitors

2017 ◽  
Vol 41 (10) ◽  
pp. 571-575 ◽  
Author(s):  
Xiu-Jian Liu ◽  
Lei Wang ◽  
Long Yin ◽  
Feng-Chang Cheng ◽  
Hui-Min Sun ◽  
...  

An efficient protocol for the synthesis of novel glycosyl-containing 1,2,4-triazolo[3,4- b][1,3,4]thiadiazole derivatives starting from the commercially available D-glucosamine hydrochloride is described by reaction of glycosyl isothiocyanate with various aminotriazoles in DMF. Glycosyl isothiocyanate is an important intermediate and synthetic methods are discussed. The acetylcholinesterase inhibitory activity of these compounds was tested by Ellman's method. It was found that most compounds exhibited over 90% inhibition and they were subsequently evaluated for their IC50 values.

MedPharmRes ◽  
2017 ◽  
Vol 1 (1) ◽  
pp. 15-25
Author(s):  
Dao Tran ◽  
Son Tran ◽  
Vi Nguyen ◽  
Tri Le ◽  
Minh Thai ◽  
...  

In this study, a total of twenty chalcones were synthesized via Claisen-Schmidt condensation reaction and evaluated for their in vitro acetylcholinesterase inhibitory activities using Ellman’s method. Molecular docking studies on acetylcholinesterase were performed to elucidate the interactions between these chalcone derivatives and acetylcholinesterase active site at the molecular level. From the series, six compounds (S1-5 and S17) exhibited strong acetylcholinesterase inhibitory activities with IC50 values below 100 µM compared to the parent unsubstituted chalcone. Compound S17 (4’-amino-2-chlorochalcone) showed the strongest acetylcholinesterase inhibitory activity in the investigated group with IC50 value of 36.10 µM. Molecular modeling studies were consistent with the results of in vitro acetylcholinesterase inhibitory activities, and chalcone S17 could be considered as a potential lead compound for the development of new acetylcholinesterase inhibitors.


2016 ◽  
Vol 40 (9) ◽  
pp. 545-548 ◽  
Author(s):  
Long Yin ◽  
Feng–Chang Cheng ◽  
Qu–Xiang Li ◽  
Wei–Wei Liu ◽  
Xiu–Jian Liu ◽  
...  

2018 ◽  
Vol 34 (1) ◽  
pp. 196-202 ◽  
Author(s):  
Gabriele A. Berwaldt ◽  
Daniela P. Gouvêa ◽  
Daniel S. da Silva ◽  
Adriana M. das Neves ◽  
Mayara S. P. Soares ◽  
...  

ARKIVOC ◽  
2009 ◽  
Vol 2009 (10) ◽  
pp. 333-348 ◽  
Author(s):  
Si-jie Liu ◽  
a Liu Yang ◽  
Zhe Jin ◽  
Er-fang Huang ◽  
David Chi Cheong Wan ◽  
...  

2013 ◽  
Vol 8 (3) ◽  
pp. 1934578X1300800
Author(s):  
Buket Bozkurt Sarikaya ◽  
Strahil Berkov ◽  
Jaume Bastida ◽  
Gulen Irem Kaya ◽  
Mustafa Ali Onur ◽  
...  

A GC-MS analysis of alkaloids in the aerial parts and bulbs of Galanthus x valentinei nothosubsp. subplicatus was performed for the first time. Totally, twenty-six alkaloids were identified, of which tazettine and galanthindole were the major ones. Acetylcholinesterase inhibitory activity of the alkaloidal extracts was determined using modified in vitro Ellman's method. Significant anticholinesterase activity was observed in the tested samples (bulbs: IC50 = 21.3 μg/mL, aerial parts: IC50 = 16.3 μg/mL).


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