Results 151 to 160 of about 49,089 (200)

Evolution and Occurrence of 1,8-Cineole (Eucalyptol) in Australian Wine

open access: yesJournal of Agricultural and Food Chemistry, 2011
A new method has been developed for the quantitation of 1,8-cineole in red and white wines using headspace solid-phase microextraction (SPME) combined with stable isotope dilution analysis (SIDA) and gas chromatography-mass spectrometry (GC-MS). An extensive survey of Australian wines (44 white and 146 red) highlighted that only red wines contained ...
Dimitra L Capone   +2 more
exaly   +5 more sources
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Differential Metabolism of 1,8–Cineole in Insects

Journal of Chemical Ecology, 2003
In order to compare the metabolism of 1,8-cineole in the pyrgo beetle, Paropsisterna tigrina, three other herbivorous insect species, Faex nigroconspersa, Chrysophtharta bimaculata, and Oxyops vitiosa, were fed 1,8-cineole leaf diets. F. nigroconspersa adults excreted predominantly 9-hydroxy-1,8-cineole (36.2% of the volatile constituents) with some ...
Ian A, Southwell   +3 more
openaire   +2 more sources

Daytime Reactions of 1,8‐Cineole in the Troposphere

ChemPhysChem, 2011
AbstractRelative rate coefficients for the gas‐phase reaction of chlorine atoms (Cl) and hydroxyl radicals (OH) with 1,8‐cineole were determined by Fourier‐transform infrared (FTIR) spectroscopy between 285 and 313 K at atmospheric pressure. The temperature dependence of both reactions shows simple Arrhenius behaviour which can be represented by the ...
Antonio A, Ceacero-Vega   +4 more
openaire   +2 more sources

Vineyard and Fermentation Studies To Elucidate the Origin of 1,8-Cineole in Australian Red Wine

open access: yesJournal of Agricultural and Food Chemistry, 2012
Preliminary investigations revealed that the proximity of Eucalyptus trees to grapevines can directly influence the concentration of the aroma compound 1,8-cineole present in the corresponding red wines.
Dimitra L Capone   +2 more
exaly   +2 more sources

Biotransformation of 1,8-Cineole by Human Liver Microsomes

Natural Product Letters, 2001
The biotransformation of 1,8-cineole has been investigated by using human liver microsomes. A single oxidized metabolite, 2-exo-hydroxy-1,8-cineole, was isolated. Its formation was investigated under various conditions by changing incubation time, P450 level in liver microsomes, and substrate concentration.
M, Miyazawa, M, Shindo
openaire   +2 more sources

The Synthesis of 1,8-Cineoles. The Origin of the Oxygen Atom

Australian Journal of Chemistry, 1997
1,8-Cineoles can be synthesized by ring closure of p -menthane precursors carrying the potential ether oxygen atom on either C1 or C8. Comparisons are made between these two routes.
Brecknell D.J., Carman R.M., Garner A.C.
openaire   +3 more sources

ChemInform Abstract: Biotransformation of 1,8‐Cineole to (+)‐2‐endo‐Hydroxy‐1,8‐cineole by Glomerella cingulata.

ChemInform, 1991
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
M. MIYAZAWA   +3 more
openaire   +1 more source

A novel cannabinoid containing a 1,8-cineol moiety

Experientia, 1977
The synthesis of a novel cannabinoid containing a 1,8-cineol moiety (1) is described. It is much less biologically active thanΔ1-tetrahydrocannabinol.
D B, Uliss   +3 more
openaire   +2 more sources

1,8-Cineole: a review of source, biological activities, and application

Journal of Asian Natural Products Research, 2020
1,8-Cineole (also known as eucalyptol) is mostly extracted from the essential oils of plants, which showed extensively pharmacological properties including anti-inflammatory and antioxidant mainly via the regulation on NF-κB and Nrf2, and was used for the treatment of respiratory diseases and cardiovascular, etc.
Zi-Min Cai   +7 more
openaire   +2 more sources

Properties of 1,8-Cineole:  A Thermophysical and Theoretical Study

The Journal of Physical Chemistry B, 2007
This paper reports on an experimental and theoretical study of 1,8-cineole, one of the main components of essential oils in different plants. The pressure-volume-temperature behavior of this fluid was evaluated accurately over wide temperature and pressure ranges and correlated successfully with the empirical TRIDEN equation.
Santiago, Aparicio   +4 more
openaire   +2 more sources

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