Functionalized aurones as inducers of NAD(P)H:quinone oxidoreductase 1 that activate AhR/XRE and Nrf2/ARE signaling pathways: Synthesis, evaluation and SAR

被引:91
作者
Lee, Chong-Yew [1 ]
Chew, Eng-Hui [1 ]
Go, Mei-Lin [1 ]
机构
[1] Natl Univ Singapore, Dept Pharm, Singapore 117543, Singapore
关键词
Aurones; Chemoprevention; NAD(P)H:quinone oxidoreductase 1; Phase II enzyme inducers; CANCER-PROTECTIVE ENZYME; GENE-EXPRESSION; HYDROCARBON RECEPTOR; QUINONE REDUCTASE; AH RECEPTOR; PHASE-I; INDUCTION; FLAVONOIDS; CHEMOPREVENTION; GLUTATHIONE;
D O I
10.1016/j.ejmech.2010.03.023
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The chemopreventive potential of functionalized aurones and related compounds as inducers of NAD(P) H:quinone oxidoreductase 1 (NQO1, EC 1.6.99.2) are described. Several 4,6-dimethoxy and 5-hydroxyaurones induced NQO1 activity of Hepa1c1c7 cells by 2-fold at submicromolar concentrations, making these the most potent inducers to be identified from this class. Mechanistically, induction of NQO1 was mediated by the activation of AhR/XRE and Nrf2/ARE pathways, indicating that aurones may be mixed activators of NQO1 induction or agents capable of exploiting the proposed cross-talk between the AhR and Nrf2 gene batteries. QSAR analysis by partial least squares projection to latent structures (PLS) identified size parameters, in particular those associated with non-polar surface areas, as an important determinant of induction activity. These were largely determined by the substitution on rings A and B. A stereoelectronic role for the exocyclic double bond as reflected in the E-LUMO term was also identified. The electrophilicity of the double bond or its effect on the conformation of the target compound are possible key features for induction activity. (c) 2010 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:2957 / 2971
页数:15
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