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  • 1
    ISSN: 1432-0738
    Keywords: Cinnamic aldehyde ; Cinnamyl alcohol ; Mercapturic acids
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Rats dosed with cinnamic aldehyde (I) excreted two mercapturic acids in the urine. The major one was identified as N-acetyl-S-(1-phenyl-3-hydroxypropyl)cysteine (V). The minor one was identified as N-acetyl-S-(1-phenyl-2-carboxy ethyl)cysteine (VI). The ratio appeared to be V∶VI=4∶1. The hydroxy mercapturic acid (V) was also isolated from urine of rats dosed with cinnamyl alcohol (II). The total mercapturic acid excretion as percentage of the dose was 14.8±1.9% for cinnamic aldehyde (250 mg/kg) (n = 4) and 8.8±1.7% for cinnamyl alcohol (n = 4) (125 mg/kg). Inhibition of the alcohol dehydrogenase by pyrazole (206 mg/kg) diminished the thioether excretion of cinnamyl alcohol to 3.3±1.4% of the dose (n = 8). Cinnamic aldehyde has been proposed to be an intermediate in the mercapturic acid formation of cinnamyl alcohol.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    International archives of occupational and environmental health 46 (1980), S. 99-109 
    ISSN: 1432-1246
    Keywords: Methyl chloride ; Glutathione conjugation ; Thioethers ; Methylthio compounds ; Mercapturic acid ; S-methylcysteine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Methyl chloride is used as a methylating agent and as a blowing agent in industrial processes. Alkylating agents and other electrophilic compounds are often detoxified in the organism through conjugation with glutathione. Glutathione conjugates are generally excreted as mercapturic acids, cysteine conjugates, or other thioethers in urine. Urine samples obtained from persons occupationally exposed to methyl chloride were examined for the presence of elevated thioether levels using a previously published non-selective procedure. No significant increases were detectable. A new assay procedure was developed for the detection of methylthio compounds in urine. The method is based on alkaline hydrolysis of urine samples and subsequent gas chromatographic determination of methyl mercaptan in the headspace of acidified hydrolysates. By application of this method a greatly increased excretion of a methylthio compound in the urine of CH3Cl-exposed workers was shown. The compound was identified as S-methylcysteine. A study of the urinary S-methylcysteine excretion in a group of workers during a seven-day shift revealed that two of six workers hardly excreted any S-methylcysteine after exposure to methyl chloride.
    Type of Medium: Electronic Resource
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