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JournalISSN: 0049-8254

Xenobiotica 

Informa
About: Xenobiotica is an academic journal published by Informa. The journal publishes majorly in the area(s): Metabolite & Pharmacokinetics. It has an ISSN identifier of 0049-8254. Over the lifetime, 5338 publications have been published receiving 120145 citations.


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Journal ArticleDOI
TL;DR: Metabonomics: understanding the metabolic responses of living systems to pathophysiological stimuli via multivariate statistical analysis of biological NMR spectroscopic data by using NMR data from Xenobiotica.
Abstract: (1999). 'Metabonomics': understanding the metabolic responses of living systems to pathophysiological stimuli via multivariate statistical analysis of biological NMR spectroscopic data. Xenobiotica: Vol. 29, No. 11, pp. 1181-1189.

3,475 citations

Journal ArticleDOI
Franz Oesch1
TL;DR: Whether a given aromatic or olefinic compound produces such an effect would depend on a variety of factors, such as the relative rate of formation and degradation of the intermediate oxirane, on its stability with respect to spontaneous isomerization to the corresponding phenol and on its chemical electrophilic reactivity.
Abstract: 1. Several aromatic and olefinic compounds are converted to intermediate arene and alkene oxides by mammalian mono-oxygenases. Intermediate arene oxides rearrange non-enzymically to phenols. Arene and alkene oxides are converted by epoxide hydrases to vicinal diols and by glutathione S-epoxide conjugases to glutathione conjugates. Due to their high electrophilic reactivity, such oxiranes also bind to proteins, RNA and DNA. Mutagenic, carcinogenic and cytotoxic effects of several aromatic and olefinic compounds appear to be due to the formation of intermediate epoxides and their reaction with tissue constituents. Whether a given aromatic or olefinic compound produces such an effect would thus depend on a variety of factors, such as the relative rate of formation and degradation of the intermediate oxirane, on its stability with respect to spontaneous isomerization to the corresponding phenol and on its chemical electrophilic reactivity.2. Epoxide hydrases, which convert such intermediate oxiranes t...

805 citations

Journal ArticleDOI
Shu-Feng Zhou1
TL;DR: Altered P-gp/MDR1 activity due to induction and/or inhibition can cause drug–drug interactions with altered drug pharmacokinetics and response, and is of great clinical importance in non-cancer-related drug therapy due to its wide-ranging effects on the absorption and excretion of a variety of drugs.
Abstract: 1. P-glycoprotein (P-gp/MDR1), one of the most clinically important transmembrane transporters in humans, is encoded by the ABCB1/MDR1 gene. Recent insights into the structural features of P-gp/MDR...

497 citations

Journal ArticleDOI
TL;DR: Both carnosol and carnosic acid stimulated DNA damage in the bleomycin assay but they scavenged hydroxyl radicals in the deoxyribose assay.
Abstract: 1. Carnosol and carnosic acid have been suggested to account for over 90% of the antioxidant properties of rosemary extract.2. Purified carnosol and carnosic acid are powerful inhibitors of lipid peroxidation in microsomal and liposomal systems, more effective than propyl gallate.3. Carnosol and carnosic acid are good scavengers of peroxyl radicals (CCl3O2) generated by pulse radiolysis, with calculated rate constants of 1–3 × 106M-1 S-1 and 2.7 × 107M-1 S-1 respectively.4. Carnosic acid reacted with HOCl in such a way as to protect the protein α1-antiproteinase against inactivation.5. Both carnosol and carnosic acid stimulated DNA damage in the bleomycin assay but they scavenged hydroxyl radicals in the deoxyribose assay. The calculated rate constants for reaction with ·OH in the deoxyribose system for carnosol and carnosic acid were 8.7 × 1010M-1 and 5.9 × 1010M-1 S-1 respectively.6. Carnosic acid appears to scavenge H2O2, but it could also act as a substrate for the peroxidase system.7. Carnosic acid a...

491 citations

Journal ArticleDOI
TL;DR: Correlations between molecular polarizability, excitation energy and biological activity are presented as a result of QSAR analysis on nitriles of varying rates of P4502E-mediated oxidative metabolism.
Abstract: 1. Structural studies are reported on a series of 20 nitriles of varying rates of P4502E-mediated oxidative metabolism.2. Parameters of molecular and electronic structure have been calculated for the generation of quantitative structure—activity relationships (QSARs) with the rates of oxidative metabolism of the nitriles, and with their acute toxicity.3. Correlations between molecular polarizability, excitation energy and biological activity are presented as a result of QSAR analysis.

427 citations

Performance
Metrics
No. of papers from the Journal in previous years
YearPapers
202329
2022102
2021143
2020160
2019160
2018135