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methyl 3-deoxy-3-{4-(4-methoxyphenyl)-1H-[1,2,3]-triazol-1-yl}-1-thio-β-D-galactopyranoside | 869957-56-2

中文名称
——
中文别名
——
英文名称
methyl 3-deoxy-3-{4-(4-methoxyphenyl)-1H-[1,2,3]-triazol-1-yl}-1-thio-β-D-galactopyranoside
英文别名
(2R,3R,4S,5R,6S)-2-(hydroxymethyl)-4-[4-(4-methoxyphenyl)triazol-1-yl]-6-methylsulfanyloxane-3,5-diol
methyl 3-deoxy-3-{4-(4-methoxyphenyl)-1H-[1,2,3]-triazol-1-yl}-1-thio-β-D-galactopyranoside化学式
CAS
869957-56-2
化学式
C16H21N3O5S
mdl
——
分子量
367.426
InChiKey
NUVARWXRYAVHHV-CWVYHPPDSA-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:
    25
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    135
  • 氢给体数:
    3
  • 氢受体数:
    8

反应信息

  • 作为产物:
    描述:
    methyl 2,4,6-tri-O-acetyl-3-deoxy-3-(4-(4-methoxyphenyl)-1H-[1,2,3]-triazol-1-yl)-1-thio-β-D-galactopyranoside甲胺 作用下, 以72%的产率得到methyl 3-deoxy-3-{4-(4-methoxyphenyl)-1H-[1,2,3]-triazol-1-yl}-1-thio-β-D-galactopyranoside
    参考文献:
    名称:
    1H-1,2,3-Triazol-1-yl thiodigalactoside derivatives as high affinity galectin-3 inhibitors
    摘要:
    Galactose C3-triazole derivatives were synthesized by Cu(I)-catalyzed cycloaddition between acetylenes and galactose C3-azido derivatives. Evaluation against galectin-3, 7, 8N (N-terminal) and 9N (N-terminal) revealed 1,4-disubstituted triazoles to be high-affinity inhibitors of galectin-3 with selectivity over galectin-7, 8N, and 9N. Conformational analysis of 1,4-di-and 1,4,5-tri-substituted galactose C3-triazoles suggested that a triazole C5-substituent interfered sterically with the galectin proteins, which explained their poor affinities compared to the corresponding 1,4-disubstituted triazoles. Introduction of two 1,4-disubstituted triazole moieties onto thiodigalactoside resulted in affinities down to 29 nM for galectin-3. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2010.05.040
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文献信息

  • NOVEL 3-TRIAZOLYL-GALACTOSIDE INHIBITORS OF GALECTINS
    申请人:Leffler Hakon
    公开号:US20070185041A1
    公开(公告)日:2007-08-09
    The present invention relates to novel compounds, the use of said compounds as a medicament as well as for the manufacture of a medicament for treatment of disorders relating to the binding of galectin to receptors in a mammal. Said galectin is preferably a galectin-3.
    本发明涉及新型化合物,以及将该化合物用作药物以及制造用于治疗哺乳动物中与galectin与受体结合相关的疾病的药物。所述的galectin通常是galectin-3。
  • US7700763B2
    申请人:——
    公开号:US7700763B2
    公开(公告)日:2010-04-20
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