Polyphenols as antioxidant/pro-oxidant compounds and donors of reducing species: relationship with human antioxidant metabolism
In this review, we have focused mainly on the study of their antioxidant and pro-oxidant
capacity, and the analysis of the oxidation of the catechol group to o-quinone. The redox …
capacity, and the analysis of the oxidation of the catechol group to o-quinone. The redox …
The metabolism and toxicity of quinones, quinonimines, quinone methides, and quinone-thioethers
TJ Monks, DC Jones - Current drug metabolism, 2002 - ingentaconnect.com
Quinones are ubiquitous in nature and constitute an important class of naturally occurring
compounds found in plants, fungi and bacteria. Human exposure to quinones therefore …
compounds found in plants, fungi and bacteria. Human exposure to quinones therefore …
Formation and biological targets of quinones: cytotoxic versus cytoprotective effects
JL Bolton, T Dunlap - Chemical research in toxicology, 2017 - ACS Publications
Quinones represent a class of toxicological intermediates, which can create a variety of
hazardous effects in vivo including, acute cytotoxicity, immunotoxicity, and carcinogenesis …
hazardous effects in vivo including, acute cytotoxicity, immunotoxicity, and carcinogenesis …
Human Family 1–4 cytochrome P450 enzymes involved in the metabolic activation of xenobiotic and physiological chemicals: an update
SP Rendic, FP Guengerich - Archives of toxicology, 2021 - Springer
This is an overview of the metabolic activation of drugs, natural products, physiological
compounds, and general chemicals by the catalytic activity of cytochrome P450 enzymes …
compounds, and general chemicals by the catalytic activity of cytochrome P450 enzymes …
Flavonoids and alkenylbenzenes: mechanisms of mutagenic action and carcinogenic risk
IMCM Rietjens, MG Boersma, H van der Woude… - Mutation Research …, 2005 - Elsevier
The present review focuses on the mechanisms of mutagenic action and the carcinogenic
risk of two categories of botanical ingredients, namely the flavonoids with quercetin as an …
risk of two categories of botanical ingredients, namely the flavonoids with quercetin as an …
Substrates, inducers, inhibitors and structure-activity relationships of human Cytochrome P450 2C9 and implications in drug development
SF Zhou, ZW Zhou, LP Yang… - Current medicinal …, 2009 - ingentaconnect.com
Cytochrome P450 2C9 (CYP2C9) is one of the most abundant CYP enzymes in the human
liver. CYP2C9 metabolizes more than 100 therapeutic drugs, including tolbutamide …
liver. CYP2C9 metabolizes more than 100 therapeutic drugs, including tolbutamide …
Myristicin and elemicin: potentially toxic alkenylbenzenes in food
ME Götz, B Sachse, B Schäfer, A Eisenreich - Foods, 2022 - mdpi.com
Alkenylbenzenes represent a group of naturally occurring substances that are synthesized
as secondary metabolites in various plants, including nutmeg and basil. Many of the …
as secondary metabolites in various plants, including nutmeg and basil. Many of the …
Mechanism-based inactivation of cytochrome P450 enzymes: chemical mechanisms, structure-activity relationships and relationship to clinical drug-drug interactions …
Cytochrome P450 constitute a superfamily of heme-containing enzymes that catalyze the
oxidative biotransformation of structurally diverse xenobiotics including drugs. Inhibition of …
oxidative biotransformation of structurally diverse xenobiotics including drugs. Inhibition of …
Peroxidative metabolism of apigenin and naringenin versus luteolin and quercetin: glutathione oxidation and conjugation
G Galati, MY Moridani, TS Chan, PJ O'Brien - Free Radical Biology and …, 2001 - Elsevier
GSH was readily depleted by a flavonoid, H2O2, and peroxidase mixture but the products
formed were dependent on the redox potential of the flavonoid. Catalytic amounts of …
formed were dependent on the redox potential of the flavonoid. Catalytic amounts of …
Molecular characteristics of catechol estrogen quinones in reactions with deoxyribonucleosides
DE Stack, J Byun, ML Gross, EG Rogan… - Chemical research in …, 1996 - ACS Publications
Estrogens can have two roles in the induction of cancer: stimulating proliferation of cells by
receptor-mediated processes, and generating electrophilic species that can covalently bind …
receptor-mediated processes, and generating electrophilic species that can covalently bind …