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N-[O-(2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)-(1->3)-O-(2,4,6-tri-O-acetyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-acetyl-1-β-D-glucopyranosyl]-o-anisoylamide | 635302-11-3

中文名称
——
中文别名
——
英文名称
N-[O-(2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)-(1->3)-O-(2,4,6-tri-O-acetyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-acetyl-1-β-D-glucopyranosyl]-o-anisoylamide
英文别名
——
N-[O-(2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)-(1->3)-O-(2,4,6-tri-O-acetyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-acetyl-1-β-D-glucopyranosyl]-o-anisoylamide化学式
CAS
635302-11-3
化学式
C66H75NO23
mdl
——
分子量
1250.31
InChiKey
UVKHWSCOZRDMBU-OCECTRDMSA-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):
    6.2
  • 重原子数:
    90.0
  • 可旋转键数:
    28.0
  • 环数:
    8.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    279.2
  • 氢给体数:
    1.0
  • 氢受体数:
    23.0

反应信息

  • 作为反应物:
    描述:
    N-[O-(2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)-(1->3)-O-(2,4,6-tri-O-acetyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-acetyl-1-β-D-glucopyranosyl]-o-anisoylamide 在 palladium on activated charcoal 氢气sodium methylate 作用下, 以 甲醇 为溶剂, 反应 7.0h, 生成 N-[O-α-D-galactopyranosyl-(1->3)-O-β-D-galactopyranosyl-(1->4)-1-β-D-glucopyranosyl]-o-anisoylamide
    参考文献:
    名称:
    Frontal Affinity Chromatography Coupled to Mass Spectrometry: An Effective Method for KdDetermination and Screening of α‐Gal Derivatives Binding to Anti‐Gal Antibodies (IgG)
    摘要:
    Frontal affinity chromatography with mass spectrometric detection (FAC/MS) was developed as an effective method for rapid determination of K-d values for alpha-Gal derivatives binding to human anti-Gal IgG antibodies. Using this method, K-d values for 23 alpha-Gal compounds were determined for the first time, including an alpha-Gal terminated N-linked oligosaccharide which mimics a single N-glycoform present on the surface of animal cells. A mixture of eight alpha-Gal derivatives, a model for an alpha-Gal compound library, was successfully screened against this anti-Gal IgG using FAC/MS. The analyte breakthrough sequence, indicated by the ion chromatogram, reflected the magnitude of the K-d values, confirming its potential application in the screening of new alpha-Gal derivatives and mimetics. Ten alpha-Gal derivatives were designed and synthesized chemically or enzymatically. Among the compounds analyzed, trivalent compound 26 demonstrated the strongest binding affinity to anti-Gal IgG with a K-d value of 3.1 muM. The alpha-Gal terminated N-linked oligosaccharide 28 had a K-d value of 8.6 muM.
    DOI:
    10.1081/car-120025323
  • 作为产物:
    描述:
    O-(2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)-(1->3)-O-(2,4,6-tri-O-acetyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-acetyl-1-β-D-glucopyranosyl azide 在 platinum(IV) oxide 氢气三乙胺 作用下, 以 乙醇二氯甲烷 为溶剂, -78.0~20.0 ℃ 、310.26 kPa 条件下, 反应 1.0h, 生成 N-[O-(2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)-(1->3)-O-(2,4,6-tri-O-acetyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-acetyl-1-β-D-glucopyranosyl]-o-anisoylamide
    参考文献:
    名称:
    Frontal Affinity Chromatography Coupled to Mass Spectrometry: An Effective Method for KdDetermination and Screening of α‐Gal Derivatives Binding to Anti‐Gal Antibodies (IgG)
    摘要:
    Frontal affinity chromatography with mass spectrometric detection (FAC/MS) was developed as an effective method for rapid determination of K-d values for alpha-Gal derivatives binding to human anti-Gal IgG antibodies. Using this method, K-d values for 23 alpha-Gal compounds were determined for the first time, including an alpha-Gal terminated N-linked oligosaccharide which mimics a single N-glycoform present on the surface of animal cells. A mixture of eight alpha-Gal derivatives, a model for an alpha-Gal compound library, was successfully screened against this anti-Gal IgG using FAC/MS. The analyte breakthrough sequence, indicated by the ion chromatogram, reflected the magnitude of the K-d values, confirming its potential application in the screening of new alpha-Gal derivatives and mimetics. Ten alpha-Gal derivatives were designed and synthesized chemically or enzymatically. Among the compounds analyzed, trivalent compound 26 demonstrated the strongest binding affinity to anti-Gal IgG with a K-d value of 3.1 muM. The alpha-Gal terminated N-linked oligosaccharide 28 had a K-d value of 8.6 muM.
    DOI:
    10.1081/car-120025323
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