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| 870192-88-4

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
870192-88-4
化学式
C72H80O24S
mdl
——
分子量
1361.48
InChiKey
CQIIXZAZEMGGCF-QQHTZJFASA-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):
    8.16
  • 重原子数:
    97.0
  • 可旋转键数:
    29.0
  • 环数:
    9.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    268.56
  • 氢给体数:
    0.0
  • 氢受体数:
    25.0

反应信息

  • 作为反应物:
    描述:
    在 2,2,6,6-tetramethyl-piperidine-N-oxyl 、 碘苯二乙酸溶剂黄146 作用下, 以 乙醚二氯甲烷 为溶剂, 生成
    参考文献:
    名称:
    Design, synthesis, and enzymatic property of a sulfur-substituted analogue of trigalacturonic acid
    摘要:
    A sulfur-substituted analogue of trigalacturonic acid (3) was synthesized. The synthesis features the application of 3-cyano-3-(tert-butyldimethylsilyl)oxypropylthioether (CSP) as a novel protective group for thiols. This analogue was designed with the expectation that it would be a stable analogous substrate for endo-polygalacturonase isolated from Stereum purpureum based on computer modeling experiments. Surface plasmon resonance experiments revealed that 3 forms a stable complex with the target enzyme. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2005.08.019
  • 作为产物:
    描述:
    methyl 2,3-di-O-acetyl-α-D-glucopyranoside吡啶 、 2,2,6,6-tetramethyl-piperidine-N-oxyl 、 碘苯二乙酸三乙基硅基三氟甲磺酸酯 、 sodium hydride 、 溶剂黄146 作用下, 以 乙醚二氯甲烷丙酮 为溶剂, 生成
    参考文献:
    名称:
    Design, synthesis, and enzymatic property of a sulfur-substituted analogue of trigalacturonic acid
    摘要:
    A sulfur-substituted analogue of trigalacturonic acid (3) was synthesized. The synthesis features the application of 3-cyano-3-(tert-butyldimethylsilyl)oxypropylthioether (CSP) as a novel protective group for thiols. This analogue was designed with the expectation that it would be a stable analogous substrate for endo-polygalacturonase isolated from Stereum purpureum based on computer modeling experiments. Surface plasmon resonance experiments revealed that 3 forms a stable complex with the target enzyme. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2005.08.019
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