| Literature DB >> 26434977 |
Ramesh Dasari1, Annelise De Carvalho2, Derek C Medellin1, Kelsey N Middleton1, Frédéric Hague3, Marie N M Volmar4, Liliya V Frolova5, Mateus F Rossato6,7, Jorge J De La Chapa8, Nicholas F Dybdal-Hargreaves9, Akshita Pillai10, Véronique Mathieu2, Snezna Rogelj5, Cara B Gonzales8, João B Calixto6,7, Antonio Evidente11, Mathieu Gautier3, Gnanasekar Munirathinam10, Rainer Glass4, Patricia Burth12, Stephen C Pelly13, Willem A L van Otterlo13, Robert Kiss2, Alexander Kornienko14.
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.Entities:
Keywords: capsaicin; capsazepine; ion channels; resiniferatoxin; vanilloid
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Year: 2015 PMID: 26434977 PMCID: PMC4831215 DOI: 10.1002/cmdc.201500360
Source DB: PubMed Journal: ChemMedChem ISSN: 1860-7179 Impact factor: 3.466