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{7-[3,4-diacetoxy-6-acetoxymethyl-5-(3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-yloxy]-2-oxo-2H-chromen-4-yl}-acetic acid methyl ester | 929549-04-2

中文名称
——
中文别名
——
英文名称
{7-[3,4-diacetoxy-6-acetoxymethyl-5-(3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-yloxy]-2-oxo-2H-chromen-4-yl}-acetic acid methyl ester
英文别名
——
{7-[3,4-diacetoxy-6-acetoxymethyl-5-(3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-yloxy]-2-oxo-2H-chromen-4-yl}-acetic acid methyl ester化学式
CAS
929549-04-2
化学式
C38H44O22
mdl
——
分子量
852.754
InChiKey
LNNHCQPWISNLHI-AWSCQIDJSA-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):
    0.51
  • 重原子数:
    60.0
  • 可旋转键数:
    15.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.55
  • 拓扑面积:
    277.53
  • 氢给体数:
    0.0
  • 氢受体数:
    22.0

反应信息

  • 作为反应物:
    描述:
    {7-[3,4-diacetoxy-6-acetoxymethyl-5-(3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-yloxy]-2-oxo-2H-chromen-4-yl}-acetic acid methyl ester甲醇 、 lithium hydroxide 、 sodium methylate 作用下, 以 四氢呋喃 为溶剂, 反应 5.0h, 生成 2-[7-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-oxochromen-4-yl]acetic acid
    参考文献:
    名称:
    Profiling of Glycosidase Activities Using Coumarin-Conjugated Glycoside Cocktails
    摘要:
    Glycosidases are a large subgroup of carbohydrate-processing enzymes that hydrolytically cleave the glycosidic bond. Glycans formed by the action of glycosidases are involved in various biological processes. Genetic abnormalities in glycosidases are associated with inherited diseases. Thus, characterization of the catalytic activities of glycosidases is of great importance. Herein, we describe a simple and rapid approach for determining glycosidase activity profiles using coumarin-conjugated glycoside cocktails.
    DOI:
    10.1021/ol062889f
  • 作为产物:
    描述:
    7-hydroxycoumarin-4-acetic acid methyl ester sodium salt 、 乙酰溴代纤维二糖四丁基硫酸氢铵sodium carbonate 作用下, 以 氯仿 为溶剂, 反应 3.0h, 以64%的产率得到{7-[3,4-diacetoxy-6-acetoxymethyl-5-(3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-yloxy]-2-oxo-2H-chromen-4-yl}-acetic acid methyl ester
    参考文献:
    名称:
    Profiling of Glycosidase Activities Using Coumarin-Conjugated Glycoside Cocktails
    摘要:
    Glycosidases are a large subgroup of carbohydrate-processing enzymes that hydrolytically cleave the glycosidic bond. Glycans formed by the action of glycosidases are involved in various biological processes. Genetic abnormalities in glycosidases are associated with inherited diseases. Thus, characterization of the catalytic activities of glycosidases is of great importance. Herein, we describe a simple and rapid approach for determining glycosidase activity profiles using coumarin-conjugated glycoside cocktails.
    DOI:
    10.1021/ol062889f
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