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ethyl (2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1->3)-(4,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-galactopyranosyl)-(1->4)-[(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1->3)]-6-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside | 419549-90-9

中文名称
——
中文别名
——
英文名称
ethyl (2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1->3)-(4,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-galactopyranosyl)-(1->4)-[(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1->3)]-6-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside
英文别名
——
ethyl (2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1->3)-(4,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-galactopyranosyl)-(1->4)-[(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1->3)]-6-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside化学式
CAS
419549-90-9
化学式
C105H106N2O20S
mdl
——
分子量
1748.06
InChiKey
UHLVMDXRWHXSTE-QZNNHUSOSA-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):
    16.7
  • 重原子数:
    128.0
  • 可旋转键数:
    39.0
  • 环数:
    17.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    222.44
  • 氢给体数:
    0.0
  • 氢受体数:
    21.0

反应信息

  • 作为反应物:
    描述:
    5-azidopentyl 2,4,6-tri-O-benzyl-α-D-galactopyranosideethyl (2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1->3)-(4,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-galactopyranosyl)-(1->4)-[(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1->3)]-6-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside 在 4 A molecular sieve 、 三氟甲烷磺酸甲酯 作用下, 以 乙醚 为溶剂, 反应 20.0h, 以54%的产率得到5-azidopentyl (2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1->3)-(4,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-galactopyranosyl)-(1->4)-[(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1->3)]-(6-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-(1->3)-2,4,6-tri...
    参考文献:
    名称:
    Synthesis of Fragments of the Glycocalyx Glycan of the ParasiteSchistosoma mansoni
    摘要:
    The chemical synthesis of alpha-L-Fucp-(1 --> 3)-beta-D-GalpNAc-(1 --> 4)-beta-D-GlcpNAc-(1 --> 3)-alpha-D-GalpO(CH2)(5)NH2, beta-D-GalpNAc-(1 --> 4)-[alpha-L-Fucp-(1 --> 3)-]beta-D-GlcpNAc-(1 --> 3)-alpha-D-GalpO(CH2)(5)NH2, and alpha-L-Fucp-(1 --> 3)-beta-D-GalpNAc-(1 --> 4)- [alpha-L-Fucp-(1 --> 3)-]beta-D-GlcpNAc-(1 --> 3)-alpha-D-GalpO(CH2)(5)NH2 is described. These structures represent fucosylated oligosaccharide fragments of the glycocalyx glycan of the cercarial stage of the parasite Schistosoma mansoni, and in protein-conjugated form they are potential diagnostics in the search for antibodies raised against the glycan in the serum of infected humans.
    DOI:
    10.1002/1521-3765(20020104)8:1<151::aid-chem151>3.0.co;2-c
  • 作为产物:
    描述:
    perbenzyl fucosyl bromideethyl (4,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-galactopyranosyl)-(1->4)-6-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside2,4,6-三甲基吡啶 、 4 A molecular sieve 、 silver trifluoromethanesulfonate 作用下, 以 二氯甲烷甲苯 为溶剂, 反应 2.0h, 以75%的产率得到ethyl (2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1->3)-(4,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-galactopyranosyl)-(1->4)-[(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1->3)]-6-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside
    参考文献:
    名称:
    Synthesis of Fragments of the Glycocalyx Glycan of the ParasiteSchistosoma mansoni
    摘要:
    The chemical synthesis of alpha-L-Fucp-(1 --> 3)-beta-D-GalpNAc-(1 --> 4)-beta-D-GlcpNAc-(1 --> 3)-alpha-D-GalpO(CH2)(5)NH2, beta-D-GalpNAc-(1 --> 4)-[alpha-L-Fucp-(1 --> 3)-]beta-D-GlcpNAc-(1 --> 3)-alpha-D-GalpO(CH2)(5)NH2, and alpha-L-Fucp-(1 --> 3)-beta-D-GalpNAc-(1 --> 4)- [alpha-L-Fucp-(1 --> 3)-]beta-D-GlcpNAc-(1 --> 3)-alpha-D-GalpO(CH2)(5)NH2 is described. These structures represent fucosylated oligosaccharide fragments of the glycocalyx glycan of the cercarial stage of the parasite Schistosoma mansoni, and in protein-conjugated form they are potential diagnostics in the search for antibodies raised against the glycan in the serum of infected humans.
    DOI:
    10.1002/1521-3765(20020104)8:1<151::aid-chem151>3.0.co;2-c
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