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| 947382-70-9

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
947382-70-9
化学式
C35H43N3O8
mdl
——
分子量
633.742
InChiKey
UDZZVVWAFIZGEK-PYCDDPRVSA-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):
    2.87
  • 重原子数:
    46.0
  • 可旋转键数:
    16.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    133.45
  • 氢给体数:
    3.0
  • 氢受体数:
    8.0

反应信息

  • 作为反应物:
    描述:
    在 palladium on activated charcoal 氢气 作用下, 以 甲醇乙酸乙酯 为溶剂, 25.0 ℃ 、101.33 kPa 条件下, 反应 12.0h, 以80%的产率得到(2S)-2-acetamido-3-[(2R,3R,4R,5R,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-N-methylpropanamide
    参考文献:
    名称:
    Serine versus Threonine Glycosylation:  The Methyl Group Causes a Drastic Alteration on the Carbohydrate Orientation and on the Surrounding Water Shell
    摘要:
    Different behavior has been observed for the psi torsion angle of the glycosidic linkages of d-GalNAc-Ser and d-GalNAc-Thr motifs, allowing the carbohydrate moiety to adopt a completely different orientation. In addition, the fact that the water pockets found in alpha-d-GalNAc-Thr differ from those obtained for its serine analogue could be related to the different capability that the two model glycopeptides have to structure the surrounding water. This fact could have important biological inferences (i.e., antifreeze activity).
    DOI:
    10.1021/ja072181b
  • 作为产物:
    描述:
    3,4,6-tri-O-benzyl-2-nitro-D-galactal 在 Ni Raney (T4) 吡啶氢气三乙胺 作用下, 以 四氢呋喃乙醇 为溶剂, 25.0 ℃ 、101.33 kPa 条件下, 反应 30.0h, 生成
    参考文献:
    名称:
    Serine versus Threonine Glycosylation:  The Methyl Group Causes a Drastic Alteration on the Carbohydrate Orientation and on the Surrounding Water Shell
    摘要:
    Different behavior has been observed for the psi torsion angle of the glycosidic linkages of d-GalNAc-Ser and d-GalNAc-Thr motifs, allowing the carbohydrate moiety to adopt a completely different orientation. In addition, the fact that the water pockets found in alpha-d-GalNAc-Thr differ from those obtained for its serine analogue could be related to the different capability that the two model glycopeptides have to structure the surrounding water. This fact could have important biological inferences (i.e., antifreeze activity).
    DOI:
    10.1021/ja072181b
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