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methyl 3,6-di-O-acetyl-2-azido-2-deoxy-4-O-(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-α-D-glucopyranoside | 796873-37-5

中文名称
——
中文别名
——
英文名称
methyl 3,6-di-O-acetyl-2-azido-2-deoxy-4-O-(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-α-D-glucopyranoside
英文别名
——
methyl 3,6-di-O-acetyl-2-azido-2-deoxy-4-O-(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-α-D-glucopyranoside化学式
CAS
796873-37-5
化学式
C45H43N3O16
mdl
——
分子量
881.847
InChiKey
WFZYFJNROYUCHB-MUKLUZQYSA-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):
    5.18
  • 重原子数:
    64.0
  • 可旋转键数:
    16.0
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    243.48
  • 氢给体数:
    0.0
  • 氢受体数:
    17.0

上下游信息

  • 上游原料
    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:
    methyl 3,6-di-O-acetyl-2-azido-2-deoxy-4-O-(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-α-D-glucopyranosidesodium methylate 作用下, 以 甲醇 为溶剂, 反应 12.0h, 生成 methyl 2-azido-2-deoxy-4-O-(β-D-glucopyranosyl)-α-D-glucopyranoside
    参考文献:
    名称:
    Synthesis of disaccharides derived from heparin and evaluation of effects on endothelial cell growth and on binding of heparin to FGF-2
    摘要:
    The disaccharide beta-D-GlcA-(1 --> 4)-alpha-D-GlcNAc-1 --> OMe and other small nonsulfated oligosaccharides related to heparin/heparan sulfate have been shown to bind to FGF and activated the fibroblast growth factor (FGF) signalling pathway in (F32) cells expressing the FGF receptor. Synthetic routes to beta-D-GlcA-(1 --> 4)-alpha-D-GlcNAc-1 --> OMe and a glucose analogue beta-D-Glc(1 --> 4)-alpha-D-GlcNAc-1 --> OMe are described. The effects of these disaccharides on endothelial cell growth, which is relevant to angiogenesis, were evaluated and it was found they did not mimic the inhibitory effects that were observed for heparin albumin (HA) and that have also been observed by monosaccharide conjugates. They did not alter bovine aortic endothelial cell (BAEC) proliferation, in the presence of FGF-2 in serum free medium or in absence of FGF-2 in serum free and complete medium. Disaccharides (10 mug/mL) reduced by 25-31% the inhibition caused by HA (10 mug/mL) on BAEC growth in serum-free medium but had no effect in complete medium. There was no evidence obtained for the binding of these oligosaccharides to FGF-2 in competition with HA by ELISA. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.carres.2004.07.018
  • 作为产物:
    描述:
    3,6-di-O-acetyl-2-azido-2-deoxy-4-O-(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-D-glucopyranose 在 三氟化硼乙醚potassium carbonate 作用下, 以 二氯甲烷 为溶剂, 反应 12.17h, 生成 methyl 3,6-di-O-acetyl-2-azido-2-deoxy-4-O-(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-α-D-glucopyranoside
    参考文献:
    名称:
    Synthesis of disaccharides derived from heparin and evaluation of effects on endothelial cell growth and on binding of heparin to FGF-2
    摘要:
    The disaccharide beta-D-GlcA-(1 --> 4)-alpha-D-GlcNAc-1 --> OMe and other small nonsulfated oligosaccharides related to heparin/heparan sulfate have been shown to bind to FGF and activated the fibroblast growth factor (FGF) signalling pathway in (F32) cells expressing the FGF receptor. Synthetic routes to beta-D-GlcA-(1 --> 4)-alpha-D-GlcNAc-1 --> OMe and a glucose analogue beta-D-Glc(1 --> 4)-alpha-D-GlcNAc-1 --> OMe are described. The effects of these disaccharides on endothelial cell growth, which is relevant to angiogenesis, were evaluated and it was found they did not mimic the inhibitory effects that were observed for heparin albumin (HA) and that have also been observed by monosaccharide conjugates. They did not alter bovine aortic endothelial cell (BAEC) proliferation, in the presence of FGF-2 in serum free medium or in absence of FGF-2 in serum free and complete medium. Disaccharides (10 mug/mL) reduced by 25-31% the inhibition caused by HA (10 mug/mL) on BAEC growth in serum-free medium but had no effect in complete medium. There was no evidence obtained for the binding of these oligosaccharides to FGF-2 in competition with HA by ELISA. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.carres.2004.07.018
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