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The extent of absorption of benzyl acetate per unit area of skin, as assessed by the recovery of its metabolites in urine, rose with increasing concentration (mg/cm 2) of the test compound on the skin. Jiang et al. The toxicokinetics of benzyl acetate after gavage differed greatly from those after dosed feed administration. Acetaldehyde is usually considered an off-odor above threshold values (herbaceous). Even though the prediction of promiscuous activities is commonly considered to be extremely difficult,29 the active‐site hydrophobicity calculated from crystal structures seems to be highly predictive of acyltransferase activity in water. In the Abdo study, the hippuric acid metabolite was present at 95 to 99% of administered radioactivity following single oral doses to rats and mice. Dermal absorption of BA was studied by applying a range of doses to a fixed area of skin on rats. A) Density plot showing the relative frequency of hydrophobicity scores within the sequence library obtained from a BLAST search based on the amino acid sequence of 3FAK. Hippuric acid is the anticipated metabolite formed by hydrolysis of the BA ester to benzyl alcohol and acetic acid, followed by oxidation of benzyl alcohol to benzoic acid and conjugation of benzoic acid with glycine. Jasmine oil is used traditionally in the treatment of various diseases like arthritis, hepatitis, conjunctivitis, gastritis, and diarrhea. The above‐described reactions were carried out for Est8 and its homologues using both benzyl alcohol (Figure 3) and 2‐phenylethanol (Figure S7) as acceptors, and the increase in activity relative to hydrolysis was plotted as a function of the organic nucleophile concentration. Recovery of the 10 mg/kg iv and oral doses was poor, but an analysis of tissues from these animals did not reveal any trace of BA-derived radioactivity. These compounds are removed during the purification stage of the crude product. Additionally, the acyltransferases appear to efficiently process different monolignols as acyl acceptors, for example, p-coumaryl (199), caffeyl (270), coniferyl (91), 5-hydroxyconiferyl (271), and sinapyl (94) alcohols. However engineering controls should be aimed for to prevent the need for ventilation. Most aldehydes found in alcoholic beverages are produced during fermentation (e.g., acetaldehyde), processing (e.g., furfural), or extraction from oak cooperage (e.g., cinnamaldehyde and vanillin). Complete hydrolysis can be rapidly obtained, if the ester is boiled under reflux with a dilute aqueous solution of either an alkali, such as sodium hydroxide, or of a strong inorganic acid, such as sulphuric or hydrochloric acid. (Souleyre et al., 2005; Defilippi et al., 2005; Li et al., 2006; Escheverría et al., 2004), strawberry (Fragaria × ananassa) (Pérez et al., 1996; Aharoni et al., 2000; Pérez et al., 2002), banana (Musa sapientum) (Beekwilder et al., 2004; Wyllie and Fellman, 2000), melon (Cucumis melo) (El-Sharkawy et al., 2005; Yahyaoui et al., 2002), grape (Vitis labrusca) (Wang and De Luca, 2005), and olive (Olea europaea) (Salas, 2004). 6B). This information has not been reviewed or verified by the Agency or any other authority. For Est8, product hydrolysis became more dominant than acyl transfer quickly after reaching a kinetic maximum at low concentrations (ca. This can be retarded by cool storage (Marais, 1986) and the presence of wine antioxidants (Roussis et al., 2005). Such complete clearance of a xenobiotic from all major tissues within 24 hr is quite unusual.

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