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| 219727-27-2

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
219727-27-2
化学式
C29H51NO18
mdl
——
分子量
701.72
InChiKey
KHWKOHYYAYODGS-JJLQQQFJSA-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):
    -4.89
  • 重原子数:
    48.0
  • 可旋转键数:
    17.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.93
  • 拓扑面积:
    292.85
  • 氢给体数:
    10.0
  • 氢受体数:
    18.0

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    在 manganese(ll) chloride 作用下, 以 二甲基亚砜 为溶剂, 反应 48.0h, 生成 8-methoxycarbonyloctyl 5-N-acetyl-α-neuraminyl-(2->3)-β-D-galactopyranosyl-(1->3)-[α-L-fucopyranosyl-(1->4)]-2-deoxy-2-(methyl α-D-galactopyranosyluronamide)-β-D-glucopyranoside
    参考文献:
    名称:
    Glycosyltransferase catalyzed assemblage of sialyl-Lewisa-saccharopeptides
    摘要:
    A series of methyl hexopyranosiduronic acids are coupled to type I disaccharide amines to give 'trisaccharides' which have the natural N-acetyl group of the type I disaccharides replaced by uronic acids (--> saccharopeptides). These saccharopeptides are surprisingly good substrates for alpha-2,3-sialyltransferase and fucosyltransferase III. The enzymes transfer N-acetylneuraminic acid and fucose, respectively, onto these acceptor substrates, despite the far reaching alterations, regio- and stereospecifically in the expected manner to yield sialyl-Lewis(a)-saccharopeptides. (C) 1998 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0008-6215(98)00229-8
  • 作为产物:
    参考文献:
    名称:
    Glycosyltransferase catalyzed assemblage of sialyl-Lewisa-saccharopeptides
    摘要:
    A series of methyl hexopyranosiduronic acids are coupled to type I disaccharide amines to give 'trisaccharides' which have the natural N-acetyl group of the type I disaccharides replaced by uronic acids (--> saccharopeptides). These saccharopeptides are surprisingly good substrates for alpha-2,3-sialyltransferase and fucosyltransferase III. The enzymes transfer N-acetylneuraminic acid and fucose, respectively, onto these acceptor substrates, despite the far reaching alterations, regio- and stereospecifically in the expected manner to yield sialyl-Lewis(a)-saccharopeptides. (C) 1998 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0008-6215(98)00229-8
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