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[4-(α-D-mannopyranosyloxy)phenyl]acetic acid | 123039-18-9

中文名称
——
中文别名
——
英文名称
[4-(α-D-mannopyranosyloxy)phenyl]acetic acid
英文别名
4-(carboxycarbonylmethyl)phenyl-α-D-mannopyranoside;2-[4-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]acetic acid
[4-(α-D-mannopyranosyloxy)phenyl]acetic acid化学式
CAS
123039-18-9
化学式
C14H18O8
mdl
——
分子量
314.292
InChiKey
YHJWCNZGHBFVTB-CYDRSHDDSA-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):
    -0.4
  • 重原子数:
    22
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    137
  • 氢给体数:
    5
  • 氢受体数:
    8

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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

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文献信息

  • Cysteine-Based Mannoside Glycoclusters: Synthetic Routes and Antiadhesive Properties
    作者:Alexander Schierholt、Mirja Hartmann、Kirsten Schwekendiek、Thisbe K. Lindhorst
    DOI:10.1002/ejoc.201000185
    日期:——
    based on cysteine. By employing the orthogonally protected amino acid as scaffold molecule, a variety of structurally varied products can be obtained according to different synthetic routes. Testing of the prepared glycoclusters as inhibitors of type 1 fimbriae mediated bacterial adhesion is reported, giving hints about the influence of sugar valency, sugar scaffolding, and the nature of the glycosidic
    基于半胱​​酸合成了不同价态的簇状甘露糖苷。采用正交保护的氨基酸作为支架分子,可以根据不同的合成路线获得多种结构变化的产品。据报道,对制备的糖簇作为 1 型菌毛介导的细菌粘附的抑制剂进行了测试,提示了该测试系统中糖价、糖支架和糖苷苷元的性质的影响。
  • Bi- and trivalent glycopeptide mannopyranosides as inhibitors of type 1 fimbriae-mediated bacterial adhesion: variation of valency, aglycon and scaffolding
    作者:Alexander Schierholt、Mirja Hartmann、Thisbe K. Lindhorst
    DOI:10.1016/j.carres.2011.04.023
    日期:2011.9
    In order to test relevant structural parameters for effective inhibition of mannose-specific bacterial adhesion, bi- and trivalent glycopeptide alpha-D-mannopyranosides were synthesized that differ in their conformational properties as well as in the spatial arrangement of attached mannosyl residues. They were tested in an inhibition adhesion assay with fluorescent Escherichia coli bacteria and testing results were referenced to the inhibitory potency of methyl alpha-D-mannopyranoside. It was shown, that besides the nature of the mannoside aglycon moiety, scaffolding of alpha-D-mannopyranosides on a peptide backbone was important for the performance of the synthesized glycopeptides as inhibitors of bacterial adhesion. (C) 2011 Elsevier Ltd. All rights reserved.
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