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Gal(b1-2)[Gal(b1-3)]Gal

中文名称
——
中文别名
——
英文名称
Gal(b1-2)[Gal(b1-3)]Gal
英文别名
(2S,3R,4S,5R,6R)-2-[(3R,4S,5S,6R)-2,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol
Gal(b1-2)[Gal(b1-3)]Gal化学式
CAS
——
化学式
C18H32O16
mdl
——
分子量
504.442
InChiKey
DABDWRSEVCYJAY-QTRWBDKJSA-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):
    -5.8
  • 重原子数:
    34
  • 可旋转键数:
    7
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    269
  • 氢给体数:
    11
  • 氢受体数:
    16

反应信息

  • 作为反应物:
    描述:
    Gal(b1-2)[Gal(b1-3)]Gal 在 sodium tetrahydroborate 作用下, 以 甲醇 为溶剂, 反应 4.0h, 以87%的产率得到2,3-di-O-(β-D-galactopyranosyl)-D-galactitol
    参考文献:
    名称:
    Selective sialylation of 2,3-di-O-(β-d-galactopyranosyl)-d-galactose catalyzed by Trypanosoma cruzi trans-sialidase
    摘要:
    Trypanosoma cruzi, the agent of Chagas' disease, expresses on its surface a trans-sialidase (TcTS) that transfers sialic acid from host glycoconjugates to terminal beta-galactopyranosyl units of parasite mucins. This process is involved in infection and pathogenesis. The trisaccharide 2,3-di-O-( beta-D-galactopyranosyl)-D-galactose 1 is an external unit in the larger oligosaccharides of the mucins and a site for sialylation. The trisaccharide was previously synthesized in our laboratory. The last step of the synthesis was the hydrogenolysis of the crystalline benzyl trisaccharide. Herein we prove that the trisaccharide 1, its alditol 3 and the benzyl glycoside 2 are good acceptors of sialic acid and effective inhibitors of the sialylation of N-acetyllactosamine catalyzed by TcTS. Furthermore, selective sialylation of the 1 3 linked galactopyranose in glycoside 2 was determined by one and two-dimensional NMR analysis. In contrast, the flexible 2,3-di-O-(beta-D-galactopyranosyl)-D-galactitol 3 is sialylated in either one of the two possible sites. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetasy.2004.11.075
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