Theoretical study of flavonoids and proline interactions.: Aqueous and gas phases

被引:24
作者
Codorniu-Hernández, E
Mesa-Ibirico, A
Montero-Cabrera, LA
Martínez-Luzardo, F
Borrmann, T
Stohrer, WD
机构
[1] Higher Inst Nucl Sci & Technol, Div Adv Studies, Havana 10600, Cuba
[2] Univ Havana, Fac Chem, Lab Computat & Theoret Chem, Havana 10400, Cuba
[3] Univ Bremen, Inst Organ Chem, D-28334 Bremen, Germany
来源
JOURNAL OF MOLECULAR STRUCTURE-THEOCHEM | 2003年 / 623卷
关键词
flavonoids; polyphenols; proline; semiempirical methods; quantum chemistry;
D O I
10.1016/S0166-1280(02)00663-2
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Flavonoids are polyphenolic compounds found in all land plants and in plant-related foods. These compounds have many positive effects, and the interaction with proline aminoacid is one of the most important characteristics. The present work shows the results of the application of the multiple minima hypersurfaces procedures, in the study of the interactions of flavonoid monomers (catechin and robinetinidin) with proline. These results are compared with experimental and classical theoretical results reported in the available literature. The most important results of this work are related with the conformations of monomers in these interactions, the preferential position of interactions and the thermodynamic stability of these complexes. All the results are successfully compared in both, gas and aqueous phases. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:63 / 73
页数:11
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