Solanocapsine derivatives as potential inhibitors of acetylcholinesterase: Synthesis, molecular docking and biological studies.

Steroids

INFIQC-CONICET, Departamento de Química Orgánica, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba, Ciudad Universitaria, X5000HUA Córdoba, Argentina. Electronic address:

Published: December 2015

AI Article Synopsis

  • The investigation of natural products is crucial in medicinal chemistry, particularly for developing treatments for Alzheimer's disease, with a focus on acetylcholinesterase (AChE) inhibitors.
  • This study involves isolating the natural compound solanocapsine, creating chemical derivatives, and assessing their AChE inhibitory activity while analyzing how structural changes affect potency.
  • Additionally, theoretical modeling was used to explore how these compounds bind to the enzyme, providing insights for future design of steroidal alkaloid-based AChE inhibitors.

Article Abstract

The investigation of natural products in medicinal chemistry is essential today. In this context, acetylcholinesterase (AChE) inhibitors comprise one type of the compounds most actively studied in the search for an effective treatment of symptoms of Alzheimer's disease. This work describes the isolation of a natural compound, solanocapsine, the preparation of its chemical derivatives, the evaluation of AChE inhibitory activity, and the structure-activity analysis of relevant cases. The influence of structural variations on the inhibitory potency was carefully investigated by modifying different reactive parts of the parent molecule. A theoretical study was also carried out into the binding mode of representative compounds to the enzyme through molecular modeling. The biological properties of the series were investigated. Through this study valuable information was obtained of steroidal alkaloid-type compounds as a starting point for the synthesis of AChE inhibitors.

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Source
http://dx.doi.org/10.1016/j.steroids.2015.09.001DOI Listing

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