“…The inhibitory potential could be improved even further by replacing a substituted cycloalkyl or straight chain alkyl group for the cycloalkyl group. Compounds 218 and 220, as a result, might be viable novel therapeutic candidates for inhibiting the BChE enzyme 257 ( Table 9 ).…”
The present review focuses on various heterocyclic scaffolds and their role in designing and developing new potential AChE and BChE inhibitors to treat AD.
“…The inhibitory potential could be improved even further by replacing a substituted cycloalkyl or straight chain alkyl group for the cycloalkyl group. Compounds 218 and 220, as a result, might be viable novel therapeutic candidates for inhibiting the BChE enzyme 257 ( Table 9 ).…”
The present review focuses on various heterocyclic scaffolds and their role in designing and developing new potential AChE and BChE inhibitors to treat AD.
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