Study on isohexenylnaphthazarins polymerization in alkaline media

被引:21
作者
Assimopoulou, AN [1 ]
Papageorgiou, VP [1 ]
机构
[1] Aristotle Univ Thessaloniki, Dept Chem Engn, Organ Chem Lab, Thessaloniki 54124, Greece
关键词
alkannin/shikonin; hydroxynaphthoquinones; quinone; polymerization;
D O I
10.1002/bmc.347
中图分类号
Q5 [生物化学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The chiral pair alkannin and shikonin (A/S) and their isohexenylnaphthazarin (IHN) esters, which are naturally occurring hydroxynaphthoquinones (HNQ), are potent pharmaceutical substances with a wide spectrum of biological activity. The stability of A/S and their derivatives during process and storage is crucial to their use as drugs, cosmetics and food additives. The influence of alkaline media and of IHN esters hydrolysis was experimentally investigated on IHN polymerization by size exclusion chromatography (SEC). It was proved that during, IHN esters hydrolysis, polymeric A/S and IHN are formed. An optimization of the hydrolysis conditions of IHN esters was also approached in terms of polymerization. Hydrolysis of IHN from a pure mixture of pigments proved preferable to that of preliminary root extracts by means of IHN polymerization, even for analytical determination; non-polar solvents are proposed for the extraction of IHN from roots, followed by hydrolysis, aiming to minimize the polymeric IHN and A/S formed. It was also proved that polymerization of IHN in alkaline media and during hydrolysis of IHN esters proceeds through the intermediate formation of semiquitiones, after acidification, coupling of semiquitiones with phenoxyl radicals results in polymeric IHN structures. Copyright (C) 2004 John Wiley Sons, Ltd.
引用
收藏
页码:508 / 522
页数:15
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