期刊论文详细信息
Molecules
Study of Coumarin-Resveratrol Hybrids as Potent Antioxidant Compounds
Maria J. Matos1  Francisco Mura2  Saleta Vazquez-Rodriguez1  Fernanda Borges1  Lourdes Santana3  Eugenio Uriarte3  Claudio Olea-Azar2 
[1] CIQUP/Departamento de Química e Bioquímica, Faculdade de Ciências, Universidade do Porto, 4169-007 Porto, Portugal; E-Mails:;Departamento de Química Inorgánica y Analítica, Facultad de Ciencias Químicas y Farmacéuticas, Universidad de Chile, Casilla 233 Santiago, Chile; E-Mail:;Departamento de Química Orgánica, Facultad de Farmacia, Universidad de Santiago de Compostela, 15782 Santiago de Compostela, Spain; E-Mails:
关键词: hydroxylated 3-phenylcoumarins;    antioxidant assays;    electrochemical study;    inhibition of ROS;    ESR;    ADME properties;   
DOI  :  10.3390/molecules20023290
来源: mdpi
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【 摘 要 】

In the present work we synthesized a selected series of hydroxylated 3-phenylcoumarins 58, with the aim of evaluating in detail their antioxidant properties. From an in depth study of the antioxidant capacity data (ORAC-FL, ESR, CV and ROS inhibition) it was concluded that these derivatives are very good antioxidants, with very interesting profiles in all the performed assays. The study of the effect of the number and position of the hydroxyl groups on the antioxidant activity was the principal aim of this study. In particular, 7-hydroxy-3-(3'-hydroxy)phenylcoumarin (8) proved to be the most active and effective antioxidant of the selected series in four of the performed assays (ORAC-FL = 11.8, capacity of scavenging hydroxyl radicals = 54%, Trolox index = 2.33 and AI30 index = 0.18). However, the presence of two hydroxyl groups on this molecule did not increase greatly the activity profile. Theoretical evaluation of ADME properties of all the derivatives was also carried out. All the compounds can act as potential candidates for preventing or minimizing the free radical overproduction in oxidative-stress related diseases. These preliminary findings encourage us to perform a future structural optimization of this family of compounds.

【 授权许可】

CC BY   
© 2015 by the authors; licensee MDPI, Basel, Switzerland.

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