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allyl 2-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-3-O-carbamoyl-α-D-galactopyranosiduronamide | 474903-50-9

中文名称
——
中文别名
——
英文名称
allyl 2-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-3-O-carbamoyl-α-D-galactopyranosiduronamide
英文别名
[(2S,3R,4S,5R,6S)-5-[(2S,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-carbamoyl-3-hydroxy-6-prop-2-enoxyoxan-4-yl] carbamate
allyl 2-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-3-O-carbamoyl-α-D-galactopyranosiduronamide化学式
CAS
474903-50-9
化学式
C18H29N3O12
mdl
——
分子量
479.441
InChiKey
KQBOKDBJWIZOJS-JNDYGTIVSA-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):
    -3.4
  • 重原子数:
    33
  • 可旋转键数:
    10
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.72
  • 拓扑面积:
    242
  • 氢给体数:
    7
  • 氢受体数:
    12

反应信息

  • 作为反应物:
    描述:
    allyl 2-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-3-O-carbamoyl-α-D-galactopyranosiduronamide乙醇 为溶剂, 反应 18.0h, 生成 3-[3-(2-{2-[2-(2-ethoxy-3,4-dioxocyclobut-1-en-1-ylamino)ethoxy]ethoxy}ethylamino)oxopropylthio]propyl 2-O-(2-acetamido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranosyl)-3-O-carbamoyl-α-D-galactopyranosiduronamide
    参考文献:
    名称:
    Synthesis of tools for raising antibodies against moenomycin epitopes and initial immunological studies
    摘要:
    The moenomycins A and C-1 as well as penta-. di- and monosaccharide analogues have been conjugated to BSA and biotin, respectively, The moenomycin A-BSA conjugates have been used to raise polyclonal antibodies. It has been demonstrated that the antisera recognize moenomycin A. (C) 2002 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4020(02)00838-4
  • 作为产物:
    描述:
    allyl 2-O-(2-acetamido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranosyl)-3-O-carbamoyl-α-D-galactopyranosiduronamide 在 lithium hydroxide 作用下, 以 甲醇 为溶剂, 反应 0.75h, 以86%的产率得到allyl 2-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-3-O-carbamoyl-α-D-galactopyranosiduronamide
    参考文献:
    名称:
    Synthesis of tools for raising antibodies against moenomycin epitopes and initial immunological studies
    摘要:
    The moenomycins A and C-1 as well as penta-. di- and monosaccharide analogues have been conjugated to BSA and biotin, respectively, The moenomycin A-BSA conjugates have been used to raise polyclonal antibodies. It has been demonstrated that the antisera recognize moenomycin A. (C) 2002 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4020(02)00838-4
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文献信息

  • Synthesis of tools for raising antibodies against moenomycin epitopes and initial immunological studies
    作者:Andrij Buchynskyy、Katherina Stembera、Dietmar Knoll、Stefan Vogel、Uwe Kempin、Astrid Biallaß (née Donnerstag)、Lothar Hennig、Matthias Findeisen、Dietrich Müller、Peter Welzel
    DOI:10.1016/s0040-4020(02)00838-4
    日期:2002.9
    The moenomycins A and C-1 as well as penta-. di- and monosaccharide analogues have been conjugated to BSA and biotin, respectively, The moenomycin A-BSA conjugates have been used to raise polyclonal antibodies. It has been demonstrated that the antisera recognize moenomycin A. (C) 2002 Elsevier Science Ltd. All rights reserved.
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