Structure−Activity Study on the Quinone/Quinone Methide Chemistry of Flavonoids

• Published in: Chemical research in toxicology Vol. 14; no. 4; pp. 398 - 408
• Main Authors: Awad, Hanem M, Boersma, Marelle G, Boeren, Sjef, van Bladeren, Peter J, Vervoort, Jacques, Rietjens, Ivonne M. C. M
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 01.04.2001
• Subjects: Benzoquinones - chemistry; Biochemie; Biochemistry; Chromatography, High Pressure Liquid; Flavonoids - chemistry; Glutathione - chemistry; Hydrogen-Ion Concentration; Indolequinones; Indoles - chemistry; Leerstoelgroep Toxicologie; Magnetic Resonance Spectroscopy; Quinones - chemistry; Structure-Activity Relationship; Sub-department of Toxicology; Toxicologie; Toxicology; VLAG
• ISSN: 0893-228X; 1520-5010
• DOI: 10.1021/tx000216e

A structure−activity study on the quinone/quinone methide chemistry of a series of 3‘,4‘-dihydroxyflavonoids was performed. Using the glutathione trapping method followed by HPLC, 1H NMR, MALDI-TOF, and LC/MS analysis to identify the glutathionyl adducts, the chemical behavior of the quinones/quinone methides of the different flavonoids could be deduced. The nature and type of mono- and diglutathionyl adducts formed from quercetin, taxifolin, luteolin, fisetin, and 3,3‘,4‘-trihydroxyflavone show how several structural elements influence the quinone/quinone methide chemistry of flavonoids. In line with previous findings, glutathionyl adduct formation for quercetin occurs at positions C6 and C8 of the A ring, due to the involvement of quinone methide-type intermediates. Elimination of the possibilities for efficient quinone methide formation by (i) the absence of the C3−OH group (luteolin), (ii) the absence of the C2C3 double bond (taxifolin), or (iii) the absence of the C5−OH group (3,3‘,4‘-trihydroxyflavone) results in glutathionyl adduct formation at the B ring due to involvement of the o-quinone isomer of the oxidized flavonoid. The extent of di- versus monoglutathionyl adduct formation was shown to depend on the ease of oxidation of the monoadduct as compared to the parent flavonoid. Finally, unexpected results obtained with fisetin provide new insight into the quinone/quinone methide chemistry of flavonoids. The regioselectivity and nature of the quinone adducts that formed appear to be dependent on pH. At pH values above the pK a for quinone protonation, glutathionyl adduct formation proceeds at the A or B ring following expected quinone/quinone methide isomerization patterns. However, decreasing the pH below this pK a results in a competing pathway in which glutathionyl adduct formation occurs in the C ring of the flavonoid, which is preceded by protonation of the quinone and accompanied by H2O adduct formation, also in the C ring of the flavonoid. All together, the data presented in this study confirm that quinone/quinone methide chemistry can be far from straightforward, but the study provides significant new data revealing an important pH dependence for the chemical behavior of this important class of electrophiles.