生物活性
化学
TRPV1型
生物化学
兴奋剂
萜类
作用机理
倍半萜
化学合成
铅化合物
立体化学
体外
受体
瞬时受体电位通道
作者
Ramesh Dasari,Annelise De Carvalho,Derek C. Medellin,Kelsey N. Middleton,Frédéric Hague,Marie N.M. Volmar,Liliya V. Frolova,Mateus F. Rossato,Jorge J. De La Chapa,Nicholas F. Dybdal‐Hargreaves,Akshita Pillai,Véronique Mathieu,Snezna Rogelj,Cara B. Gonzales,João Β. Calixto,Antonio Evidente,Mathieu Gautier,Gnanasekar Munirathinam,Rainer Glaß,Patrícia Burth
出处
期刊:ChemMedChem
[Wiley]
日期:2015-10-05
卷期号:10 (12): 2014-2026
被引量:22
标识
DOI:10.1002/cmdc.201500360
摘要
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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