Alkyl 2-(2-(arylidene)alkylhydrazinyl)thiazole-4-carboxylates: Synthesis, Acetyl cholinesterase inhibition and docking studies

2021 ◽  
pp. 131063
Author(s):  
Muhammad Haroon ◽  
Muhammad Khalid ◽  
Kiran Shahzadi ◽  
Tashfeen Akhtar ◽  
Sumbal Saba ◽  
...  
2020 ◽  
Vol 2 ◽  
pp. 100041 ◽  
Author(s):  
Naheed Riaz ◽  
Muhammad Iftikhar ◽  
Muhammad Saleem ◽  
Aziz-ur-Rehman ◽  
Safdar Hussain ◽  
...  

Planta Medica ◽  
2015 ◽  
Vol 82 (01/02) ◽  
pp. 138-146 ◽  
Author(s):  
Mohamed-Elamir Hegazy ◽  
Abeer Ibrahim ◽  
Tarik Mohamed ◽  
Abdelaaty Shahat ◽  
Ali El Halawany ◽  
...  

2013 ◽  
Vol 3 (2) ◽  
pp. 111-118 ◽  
Author(s):  
C. T. Sulaiman ◽  
C. T Sadashiva ◽  
Satheesh George ◽  
V. K Goplakrishnan ◽  
Indira Balachandran

RSC Advances ◽  
2022 ◽  
Vol 12 (3) ◽  
pp. 1788-1796
Author(s):  
Saba Mehreen ◽  
Aman Ullah ◽  
Humaira Nadeem ◽  
Necmi Dege ◽  
Muhammad Moazzam Naseer

The phenoxy pendant isatins were observed to be highly potent inhibitors of acetylcholinesterase. In addition, the solid-state structure of a phenoxy pendant isatin showed an intriguing 1D-supramolecular self-assembled structure.


2007 ◽  
Vol 2 (7) ◽  
pp. 1934578X0700200 ◽  
Author(s):  
Monica Rosa Loizzo ◽  
Rosa Tundis ◽  
Federica Menichini ◽  
Marco Bonesi ◽  
Giancarlo Antonio Statti ◽  
...  

Extracts, linariin, isolinariin A and B obtained from Linaria reflexa Desf. (Scrophulariaceae) were tested for acetylcholinesterase inhibition activity using Ellman's method. A dose-response relationship was observed for all extracts and isolated compounds. Flavones exhibited IC50 values ranging from 0.27 μM to 0.30 μM. The structure-activity relationship was briefly discussed.


2016 ◽  
Vol 258 ◽  
pp. S113-S114
Author(s):  
R.C. Tincu ◽  
C. Cobilinschi ◽  
D. Tomescu ◽  
Z. Ghiorghiu ◽  
R.A. Macovei

Author(s):  
Hélimar Gonçalves de Lima ◽  
Francianne Oliveira Santos ◽  
Acidália Carine Vieira Santos ◽  
Gisele Dias da Silva ◽  
Rafaela Jesus dos Santos ◽  
...  

Abstract We investigated the in vitro acaricide activity of the methanolic extract (ME) and alkaloid-rich fraction (AF) of Prosopis juliflora on Rhipicephalus microplus and correlated this effect with acetylcholinesterase (AChE) inhibition. The acaricide activity was evaluated using adult and larval immersion tests. Also, we studied the possible interaction mechanism of the major alkaloids present in this fraction via molecular docking at the active site of R. microplus AChE1 (RmAChE1). Higher reproductive inhibitory activity of the AF was recorded, with effective concentration (EC50) four times lower than that of the ME (31.6 versus 121 mg/mL). The AF caused mortality of tick larvae, with lethal concentration 50% (LC50) of 13.8 mg/mL. Both ME and AF were seen to have anticholinesterase activity on AChE of R. microplus larvae, while AF was more active with half-maximal inhibitory concentration (IC50) of 0.041 mg/mL. The LC-MS/MS analyses on the AF led to identification of three alkaloids: prosopine (1), juliprosinine (2) and juliprosopine (3). The molecular docking studies revealed that these alkaloids had interactions at the active site of the RmAChE1, mainly relating to hydrogen bonds and cation-pi interactions. We concluded that the alkaloids of P. juliflora showed acaricide activity on R. microplus and acted through an anticholinesterase mechanism.


2017 ◽  
Vol 11 (5) ◽  
pp. 462-467 ◽  
Author(s):  
Zühal Güvenalp ◽  
Hilal Özbek ◽  
Kadir Özden Yerdelen ◽  
Gülderen Yılmaz ◽  
Cavit Kazaz ◽  
...  

Author(s):  
Raquel Bianca Marchesine de Almeida ◽  
Rodrigo Souza Conceição ◽  
Kryzia Santana da Silva ◽  
Manoelito Coelho dos Santos Junior ◽  
Alexsandro Branco ◽  
...  

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