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A model system study of the inhibition of heterocyclic aromatic amine formation by organosulfur compounds.

机译:对有机硫化合物抑制杂环芳香胺形成的模型系统研究。

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Organosulfur compounds and sodium bisulfite significantly inhibited (P < 0.05) heterocyclic aromatic amine (HAA) formation in model systems containing phenylalanine, creatinine, and glucose. There was, however, no inhibition by the same compounds in a model system containing only phenylalanine and creatinine. Diallyl disulfide (DAD) and dipropyl disulfide (DPD) concentrations in the model systems were significantly decreased (P < 0.05) after heating for 10 min at 180 degrees C. Only very low concentrations of sulfhydryl groups (4.19 and 4.00 micromol) were produced on heating DAD and DPD for 30 min. Reaction of glucose and DAD produced several sulfur-containing compounds. After 10 min of heating at 180 degrees C, HAA formation in the control model systems was increased significantly, and DAD was an effective inhibitor during this heating period. Tetrahydrothiophene-3-one (THT) and tetrahydrothiophene (THP); two products resulting from the interaction of glucose and DAD, had no direct influence on HAA formation in the model systems.
机译:在包含苯丙氨酸,肌酐和葡萄糖的模型系统中,有机硫化合物和亚硫酸氢钠显着抑制(P <0.05)杂环芳香胺(HAA)的形成。但是,在仅包含苯丙氨酸和肌酸酐的模型系统中,相同的化合物没有抑制作用。在180摄氏度下加热10分钟后,模型系统中的二烯丙基二硫(DAD)和二丙基二硫(DPD)浓度显着降低(P <0.05)。在此条件下,仅产生非常低浓度的巯基(4.19和4.00 micromol)。将DAD和DPD加热30分钟。葡萄糖和DAD的反应产生了几种含硫化合物。在180摄氏度下加热10分钟后,对照模型系统中的HAA形成显着增加,在此加热期间DAD是有效的抑制剂。四氢噻吩-3-酮(THT)和四氢噻吩(THP);葡萄糖和DAD相互作用产生的两种产物对模型系统中HAA的形成没有直接影响。

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