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Sprague-Dawley rat liver cytosol

中文名称
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中文别名
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英文名称
Sprague-Dawley rat liver cytosol
英文别名
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CAS
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化学式
mdl
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分子量
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InChiKey
——
BEILSTEIN
——
EINECS
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  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

反应信息

  • 作为试剂:
    描述:
    参考文献:
    名称:
    Rapid conversion of tea catechins to monomethylated products by rat liver cytosolic catechol-O-methyltransferase
    摘要:
    1. The metabolic O-methylation of several catechol-containing tea polyphenols by rat liver cytosolic catechol-O-methyltransferase (COMT) has been studied.2. When (-)-epicatechin was used as substrate, its O-methylation showed dependence on incubation time, cytosolic protein concentration, incubation pH and concentration of S-adenosyl-L-methionine. The O-methylation of increasing concentrations of (-)epicatechin followed typical Michaelis-Menten kinetics, and the apparent K-m and V-max were 51 muM and 2882 pmol mg protein(-1) min(-1), respectively, at pH 7.4, and were 17 muM and 2093 pmol mg protein(-1) min(-1), respectively, at pH 10.0.3. Under optimized conditions for in vitro O-methylation, (-)-epicatechin, epicatechin and (-)-epigallocatechin were rapidly O-methylated by rat liver cytosol. In comparison, (-)-epicatechin gallate and (-)-epigallocatechin gallate were O-methylated at significantly lower rates under the same reaction conditions.4. COMT-catalysed O-methylation of (-)-epicatechin and (-)-epigallocatechin was inhibited in a concentration-dependent manner by S-adenosyl-L-homocysteine, a demethylated product of S-adenosyl-L-methionine. The IC50 was similar to 10 muM.5. In summary, the results showed that several catechol-containing tea polyphenols were rapidly O-methylated by rat liver cytosolic COMT. These observations raise the possibility that some of the biological effects of tea polyphenols may be exerted by their O-methylated products or may result from their potential inhibition of the COMT-catalysed O-methylation of endogenous catecholamines and catechol oestrogens.
    DOI:
    10.1080/00498250110079798
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