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PMID: 17504197 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Phenolic Michael reaction acceptors: combined direct and indirect antioxidant defenses against electrophiles and oxidants.

Medicinal chemistry (Shariqah (United Arab Emirates)) ·Vol. 3 ·No. 3 ·2007-05-00 ·Pages 261-8

Dinkova-Kostova AT, Cheah J, Samouilov A, Zweier JL, Bozak RE, Hicks RJ, Talalay P

Abstract

The implications of oxidative stress in the pathogenesis of many chronic human diseases has led to the widely accepted view that low molecular weight antioxidants could be beneficial and postpone or even prevent these diseases. Small molecules of either plant or synthetic origins, which contain Michael acceptor functionalities (olefins or acetylenes conjugated to electron-withdrawing groups) protect against the toxicity of oxidants and electrophiles indirectly, i.e., by inducing phase 2 cytoprotective enzymes. Some of these molecules, e.g., flavonoid and curcuminoid analogues that have phenolic hydroxyl groups in addition to Michael acceptor centers, are also potent direct antioxidants, and may therefore be appropriately designated: bifunctional antioxidants. By use of spectroscopic methods we identified phenolic chalcone and bis(benzylidene)acetone analogues containing one or two Michael acceptor groups, respectively, as very efficient scavengers of two different types of radicals: (a) the nitrogen-centered 2,2'-azinobis-(3-ethyl-benzothiazoline-6-sulfonic acid) (ABTS.+) radical cation, and (b) the oxygen-centered galvinoxyl (phenoxyl) radical. The most potent scavengers are those also bearing hydroxyl substituents on the aromatic ring(s) at the ortho-position(s). The initial reaction velocities are very rapid and concentration-dependent. In the human keratinocyte cell line HaCaT, the same compounds coordinately increase the intracellular levels of glutathione, glutathione reductase, and thioredoxin reductase. Thus, such bifunctional antioxidants could exert synergistic protective effects against oxidants and electrophiles which represent the principal biological hazards by: (i) scavenging hazardous oxidants directly and immediately; and (ii) inducing the phase 2 response to prevent and resolve the consequences of hazardous processes that are already in progress, i.e., acting indirectly, but with much more diverse and long-lasting effects.

MeSH Terms
Antioxidants/chemistry Free Radical Scavengers/chemistry Oxidants/chemistry Phenols/chemistry Structure-Activity Relationship
Chemicals
Antioxidants Free Radical Scavengers Oxidants Phenols
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Dinkova-Kostova A T
The Lewis B and Dorothy Cullman Cancer Chemoprotection Center, Department of Pharmacology, and Moleclar Sciences, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA. [email protected]
Cheah J
Samouilov A
Zweier J L
Bozak R E
Hicks R J
Talalay P
Article Info
Journal
Medicinal chemistry (Shariqah (United Arab Emirates))
Abbr.
Med Chem
ISSN
1573-4064
Published
2007-05-00
Pages
261-8
Language
English
Region
Netherlands
NLM ID
101240303
Subset
IM
Grants
NCI NIH HHS · CA094076 · United States
NHLBI NIH HHS · HL38324 · United States
NHLBI NIH HHS · HL63744 · United States
NHLBI NIH HHS · HL65608 · United States
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