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glutathionesulfonic acid | 1512836-09-7

中文名称
——
中文别名
——
英文名称
glutathionesulfonic acid
英文别名
——
glutathionesulfonic acid化学式
CAS
1512836-09-7
化学式
C10H17N3O9S
mdl
——
分子量
359.286
InChiKey
QGWRMTHFAZVWAM-GOVIAEJFSA-N
BEILSTEIN
——
EINECS
——
  • 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

计算性质

  • 辛醇/水分配系数(LogP):
    -3.25
  • 重原子数:
    23.0
  • 可旋转键数:
    10.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    213.19
  • 氢给体数:
    6.0
  • 氢受体数:
    7.0

反应信息

  • 作为产物:
    描述:
    参考文献:
    名称:
    Quantitation of glutathione and its oxidation products in erythrocytes by multiple-label stable-isotope dilution
    摘要:
    A multiple-label stable isotope dilution assay for quantifying glutathione (GSH), glutathione disulfide (GSSG), and glutathione sulfonic acid in erythrocytes was developed. As the internal standards, [C-13(3),N-15]glutathione, [C-13(4),N-15(2)]glutathione disulfide, and [C-13(3),N-15]glutathione sulfonic acid were used. Analytes and internal standards were detected by LC-MS/MS after derivatization of GSH with iodoacetic acid and dansylation of all compounds under study. The calibration functions for all analytes relative to their respective isotopologic standards revealed slopes close to 1.0 and negligible intercepts. As various labelings of the standards for GSH and GSSG were used, their simultaneous quantitation was possible, although GSH was partly oxidized to its disulfide during analysis. The degree of this artifact formation of GSSG was calculated from the abundance of the mixed disulfide formed from unlabeled GSH and its respective standard. Thus, the detected GSSG amount could be corrected for the artifact amount. In this way, the amount of GSSG in erythrocytes was found to be less than 0.5% of the GSH concentration. Similar to GSSG, the detected amount of glutathione sulfonic acid was found to be formed at least in part during the analytical process, but the degree could not be quantified. (C) 2013 Elsevier Inc. All rights reserved.
    DOI:
    10.1016/j.ab.2013.09.029
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