TY - JOUR
T1 - Synthetic and Biological Studies of Sesquiterpene Polygodial
T2 - Activity of 9-Epipolygodial against Drug-Resistant Cancer Cells
AU - Dasari, Ramesh
AU - De Carvalho, Annelise
AU - Medellin, Derek C.
AU - Middleton, Kelsey N.
AU - Hague, Frédéric
AU - Volmar, Marie N.M.
AU - Frolova, Liliya V.
AU - Rossato, Mateus F.
AU - De La Chapa, Jorge J.
AU - Dybdal-Hargreaves, Nicholas F.
AU - Pillai, Akshita
AU - Mathieu, Véronique
AU - Rogelj, Snezna
AU - Gonzales, Cara B.
AU - Calixto, João B.
AU - Evidente, Antonio
AU - Gautier, Mathieu
AU - Munirathinam, Gnanasekar
AU - Glass, Rainer
AU - Burth, Patricia
AU - Pelly, Stephen C.
AU - Van Otterlo, Willem A.L.
AU - Kiss, Robert
AU - Kornienko, Alexander
N1 - Publisher Copyright:
© 2015 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
PY - 2015/12/1
Y1 - 2015/12/1
N2 - 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.
AB - 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.
KW - capsaicin
KW - capsazepine
KW - ion channels
KW - resiniferatoxin
KW - vanilloid
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U2 - 10.1002/cmdc.201500360
DO - 10.1002/cmdc.201500360
M3 - Article
C2 - 26434977
AN - SCOPUS:84949740662
SN - 1860-7179
VL - 10
SP - 2014
EP - 2026
JO - ChemMedChem
JF - ChemMedChem
IS - 12
ER -