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2-propyl 3-deoxy-4-S-(β-D-galactofuranosyl)-4-thio-α-D-xylohexopyranoside | 1153941-17-3

中文名称
——
中文别名
——
英文名称
2-propyl 3-deoxy-4-S-(β-D-galactofuranosyl)-4-thio-α-D-xylohexopyranoside
英文别名
——
2-propyl 3-deoxy-4-S-(β-D-galactofuranosyl)-4-thio-α-D-xylohexopyranoside化学式
CAS
1153941-17-3
化学式
C15H28O9S
mdl
——
分子量
384.448
InChiKey
LZZWVFOHWDLFCL-PXGYEIKCSA-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

物化性质

  • 沸点:
    681.2±55.0 °C(predicted)
  • 密度:
    1.47±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -2.22
  • 重原子数:
    25.0
  • 可旋转键数:
    7.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    149.07
  • 氢给体数:
    6.0
  • 氢受体数:
    10.0

反应信息

  • 作为产物:
    描述:
    2-propyl 6-O-acetyl-3-deoxy-4-S-(2,3,5,6-tetra-O-benzoyl-β-D-galactofuranosyl)-4-thio-α-D-xylohexopyranoside三乙胺 作用下, 以 甲醇 为溶剂, 以92%的产率得到2-propyl 3-deoxy-4-S-(β-D-galactofuranosyl)-4-thio-α-D-xylohexopyranoside
    参考文献:
    名称:
    Thiodisaccharides with galactofuranose or arabinofuranose as terminal units: Synthesis and inhibitory activity of an exo β-d-galactofuranosidase
    摘要:
    Thiodisaccharides having beta-D-Galf or alpha-L-Araf units as non-reducing end have been synthesized by the SnCl4- or MoO2Cl2-promoted thioglycosylation of per-O-benzoyl-D-galactofuranose (1), its 1-O-acetyl analogue 4, or per-O-acetyl-alpha-L-arabinofuranose (16) with 6-thioglucose or 6-thiogalactose derivatives. After convenient removal of the protecting groups, the free thiodisaccharides having the basic structure beta-D-Galf(1 -> 6)-6-thio-alpha-D-Glcp-OMe (5) or beta-D-Galf(1 -> 6)-6-thio-alpha-D-Galp-OMe (15) were obtained. The respective alpha-L-Araf analogues 18 and 20 were prepared similarly from 16. Alternatively, beta-D-Galf(1 -> 4)-4-thio- 3-deoxy-alpha-L-Xylp-OiPr was synthesized by Michael addition to a sugar enone of 1-thio-beta-D-Galf derivative, generated in situ from the glycosyl isothiourea derivative of 1. The free S-linked disaccharides were evaluated as inhibitors of the beta-galactofuranosidase from Penicillium fellutanum, being 15 and 20 the more active inhibitors against this enzyme. (c) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2009.02.045
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