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methyl 4-{[6-azido-6-deoxy-4-O-(β-D-galactopyranosyl)-β-D-glucopyranosyl]oxy}benzoate | 1134643-94-9

中文名称
——
中文别名
——
英文名称
methyl 4-{[6-azido-6-deoxy-4-O-(β-D-galactopyranosyl)-β-D-glucopyranosyl]oxy}benzoate
英文别名
methyl 4-[(2S,3R,4R,5S,6R)-6-(azidomethyl)-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxybenzoate
methyl 4-{[6-azido-6-deoxy-4-O-(β-D-galactopyranosyl)-β-D-glucopyranosyl]oxy}benzoate化学式
CAS
1134643-94-9
化学式
C20H27N3O12
mdl
——
分子量
501.447
InChiKey
NYMXJZAGTCTSAF-WNTITPJBSA-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):
    -0.9
  • 重原子数:
    35
  • 可旋转键数:
    9
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.65
  • 拓扑面积:
    199
  • 氢给体数:
    6
  • 氢受体数:
    14

反应信息

  • 作为反应物:
    参考文献:
    名称:
    C(6)或C(6')修饰的4-(甲氧羰基)苯基β-乳糖苷衍生物的合成及其对赤藓菌凝集素介导的血凝反应的抑制活性评估
    摘要:
    Abstractmagnified imageWe report herein the synthesis of 4‐(methoxycarbonyl)phenyl β‐lactoside and eight derivatives modified at C(6) or C(6′). These compounds were evaluated in hemagglutination inhibition assay using the lectin from Erythrina cristagalli. None of the compounds showed enhanced activity as compared to lactose.
    DOI:
    10.1002/hlca.200800239
  • 作为产物:
    描述:
    methyl 4-{[6-deoxy-4-O-(β-D-galactopyranosyl)-6-iodo-β-D-glucopyranosyl]oxy}benzoate 在 sodium azide 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 24.0h, 以87%的产率得到methyl 4-{[6-azido-6-deoxy-4-O-(β-D-galactopyranosyl)-β-D-glucopyranosyl]oxy}benzoate
    参考文献:
    名称:
    C(6)或C(6')修饰的4-(甲氧羰基)苯基β-乳糖苷衍生物的合成及其对赤藓菌凝集素介导的血凝反应的抑制活性评估
    摘要:
    Abstractmagnified imageWe report herein the synthesis of 4‐(methoxycarbonyl)phenyl β‐lactoside and eight derivatives modified at C(6) or C(6′). These compounds were evaluated in hemagglutination inhibition assay using the lectin from Erythrina cristagalli. None of the compounds showed enhanced activity as compared to lactose.
    DOI:
    10.1002/hlca.200800239
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文献信息

  • Synthesis of 4-(Methoxycarbonyl)phenyl<i>β</i>-Lactoside Derivatives Modified at C(6) or C(6′), and Evaluation of Their Inhibitory Activity on<i>Erythrina cristagalli</i>Lectin-Mediated Hemagglutination
    作者:Anna Paola Butera、José Dias de Souza Filho、Maria Auxiliadôra Fontes Prado、Marilda Pereira Lisboa、Ricardo José Alves
    DOI:10.1002/hlca.200800239
    日期:2009.1
    Abstractmagnified imageWe report herein the synthesis of 4‐(methoxycarbonyl)phenyl β‐lactoside and eight derivatives modified at C(6) or C(6′). These compounds were evaluated in hemagglutination inhibition assay using the lectin from Erythrina cristagalli. None of the compounds showed enhanced activity as compared to lactose.
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