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Synthetic and Biological Studies of Sesquiterpene Polygodial: Activity of 9-Epipolygodial against Drug-Resistant Cancer Cells. | LitMetric

AI Article Synopsis

  • Polygodial, a compound from the plant Polygonum hydropiper, acts as an agonist for the TRPV1 receptor and has potential anticancer properties.
  • Researchers created various analogues of polygodial, identifying 9-epipolygodial, which showed stronger antiproliferative effects than polygodial, especially against cancer cells resistant to apoptosis and multidrug resistance.
  • The study also confirmed a proposed mechanism of action for polygodial by producing a stable derivative, highlighting its chemical properties and suggesting further research for new drug development and understanding how natural products can modify biological molecules.

Article Abstract

Polygodial, a terpenoid dialdehyde isolated from Polygonum hydropiper L., is a known agonist of the transient receptor potential vanilloid 1 (TRPV1). In this investigation a series of polygodial analogues were prepared and investigated for TRPV1-agonist and anticancer activities. These experiments led to the identification of 9-epipolygodial, which has antiproliferative potency significantly exceeding that of polygodial. 9-Epipolygodial was found to maintain potency against apoptosis-resistant cancer cells as well as those displaying the multidrug-resistant (MDR) phenotype. In addition, the chemical feasibility for the previously proposed mechanism of action of polygodial, involving the formation of a Paal-Knorr pyrrole with a lysine residue on the target protein, was demonstrated by the synthesis of a stable polygodial pyrrole derivative. These studies reveal rich chemical and biological properties associated with polygodial and its direct derivatives. These compounds should inspire further work in this area aimed at the development of new pharmacological agents, or the exploration of novel mechanisms of covalent modification of biological molecules with natural products.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4831215PMC
http://dx.doi.org/10.1002/cmdc.201500360DOI Listing

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