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Design and synthesis of some acridine‐piperazine hybrids for the improvement of cognitive dysfunction
Author(s) -
Sharma Anuradha,
Piplani Poonam
Publication year - 2017
Publication title -
chemical biology and drug design
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.59
H-Index - 77
eISSN - 1747-0285
pISSN - 1747-0277
DOI - 10.1111/cbdd.13017
Subject(s) - piperazine , acridine , cognition , hybrid , chemistry , combinatorial chemistry , computational biology , biology , computer science , pharmacology , neuroscience , genetics , botany
A novel series of hybrid molecules ( 5a–5m ) was designed, synthesized and evaluated as multifunctional cholinesterase (ChE) inhibitors against cognitive dysfunction. Heterocyclic moieties acridine and piperazine were conjugated with suitable linkers in a single scaffold, and the structures of the target compounds were confirmed by IR , 1 H NMR , 13 C NMR , and LC ‐ MS analysis. The pharmacological activity of synthesized compounds was evaluated using behavioral models of amnesia viz. step‐down passive avoidance and elevated plus maze at a dose 0.5 mg/kg as compared to standard rivastigmine. In vitro acetylcholinesterase ( AC hE) inhibition studies using brain homogenate of mice as the enzyme source revealed that most of the compounds exhibited a significant ability to inhibit the enzyme cholinesterase with compound 5c being the most potent ( IC 50 0.33 μ m ). Biochemical estimation of oxidative stress markers viz. plasma nitrite, thiobarbituric acid reactive substances, catalase, superoxide dismutase, and glutathione has been carried out using the respective assays to see the effect of the synthesized compounds on the scopolamine‐induced oxidative damage. The molecular docking studies indicated the binding mode of the compounds to the catalytic site, peripheral site, and mid‐gorge of AC hE simultaneously. The calculated absorption, distribution, metabolism and excretion properties ensured the drug‐likeness of the target compounds. The synthesized compounds were found to be potential cognitive enhancers, which were able to interfere with the scopolamine‐induced oxidative stress also.