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(11-azidoundecyl 5-acetamido-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranosid)onic acid | 1338224-95-5

中文名称
——
中文别名
——
英文名称
(11-azidoundecyl 5-acetamido-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranosid)onic acid
英文别名
(2R,4S,5R,6R)-5-acetamido-2-(11-azidoundecoxy)-4-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxane-2-carboxylic acid
(11-azidoundecyl 5-acetamido-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranosid)onic acid化学式
CAS
1338224-95-5
化学式
C22H40N4O9
mdl
——
分子量
504.581
InChiKey
UAFWVTZTOSZUGO-ZJGVECAJSA-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):
    2.1
  • 重原子数:
    35
  • 可旋转键数:
    18
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.91
  • 拓扑面积:
    180
  • 氢给体数:
    6
  • 氢受体数:
    11

反应信息

  • 作为反应物:
    描述:
    (11-azidoundecyl 5-acetamido-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranosid)onic acid胞苷-5'-单磷酸-N-乙酰神经氨酸 在 CST-II 、 manganese(ll) chloride 、 alkaline phosphatase 作用下, 以 为溶剂, 反应 24.0h, 以12%的产率得到11-azidoundecyl O-(5-acetamido-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranosylonic acid)-(2->8)-5-acetamido-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranosidonic acid
    参考文献:
    名称:
    CST-II’s recognition domain for acceptor substrates in α-(2→8)-sialylations
    摘要:
    CST-II is a bacterial sialyltransferase known for its ability to perform alpha-(2 -> 8)-sialylations using GM(3) related trisaccharide substrates. Previously, we probed the enzyme's substrate specificity and developed an efficient synthesis for alpha-(2 -> 8)-oligosialosides, and we suggested that CST-II could have a very small substrate recognition domain. Here we report our full studies on CST-II's recognition feature for acceptor substrates. The current study further demonstrates the versatility of CST-II in preparing complex oligosaccharides that contain alpha-(2 -> 8)-oligosialyl moieties. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.carres.2011.05.009
  • 作为产物:
    描述:
    methyl (11-azidoundecyl 5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranosid)onate 在 sodium methylate 作用下, 以 甲醇 为溶剂, 反应 0.5h, 以64%的产率得到(11-azidoundecyl 5-acetamido-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranosid)onic acid
    参考文献:
    名称:
    CST-II’s recognition domain for acceptor substrates in α-(2→8)-sialylations
    摘要:
    CST-II is a bacterial sialyltransferase known for its ability to perform alpha-(2 -> 8)-sialylations using GM(3) related trisaccharide substrates. Previously, we probed the enzyme's substrate specificity and developed an efficient synthesis for alpha-(2 -> 8)-oligosialosides, and we suggested that CST-II could have a very small substrate recognition domain. Here we report our full studies on CST-II's recognition feature for acceptor substrates. The current study further demonstrates the versatility of CST-II in preparing complex oligosaccharides that contain alpha-(2 -> 8)-oligosialyl moieties. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.carres.2011.05.009
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文献信息

  • CST-II’s recognition domain for acceptor substrates in α-(2→8)-sialylations
    作者:Wenling Li、Ping Zhang、Amir J. Zuccolo、Ruxiang Blake Zheng、Chang-Chun Ling
    DOI:10.1016/j.carres.2011.05.009
    日期:2011.9
    CST-II is a bacterial sialyltransferase known for its ability to perform alpha-(2 -> 8)-sialylations using GM(3) related trisaccharide substrates. Previously, we probed the enzyme's substrate specificity and developed an efficient synthesis for alpha-(2 -> 8)-oligosialosides, and we suggested that CST-II could have a very small substrate recognition domain. Here we report our full studies on CST-II's recognition feature for acceptor substrates. The current study further demonstrates the versatility of CST-II in preparing complex oligosaccharides that contain alpha-(2 -> 8)-oligosialyl moieties. (C) 2011 Elsevier Ltd. All rights reserved.
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