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2-propenyl 2,4-O-benzyl-3-O-(2,4,6-tri-O-benzyl-α-D-galactopyranosyl)-β-D-galactopyranoside | 389119-80-6

中文名称
——
中文别名
——
英文名称
2-propenyl 2,4-O-benzyl-3-O-(2,4,6-tri-O-benzyl-α-D-galactopyranosyl)-β-D-galactopyranoside
英文别名
Bn(-2)[Bn(-4)][Bn(-6)]Gal(a1-3)[Bn(-2)][Bn(-4)]Gal(b)-O-allyl;(2R,3R,4S,5R,6R)-2-[(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-3,5-bis(phenylmethoxy)-6-prop-2-enoxyoxan-4-yl]oxy-3,5-bis(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-4-ol
2-propenyl 2,4-O-benzyl-3-O-(2,4,6-tri-O-benzyl-α-D-galactopyranosyl)-β-D-galactopyranoside化学式
CAS
389119-80-6
化学式
C50H56O11
mdl
——
分子量
832.988
InChiKey
VLQVQRNMSHPCKU-SDHSHHCNSA-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):
    6
  • 重原子数:
    61
  • 可旋转键数:
    22
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    124
  • 氢给体数:
    2
  • 氢受体数:
    11

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    2-propenyl 2,4-O-benzyl-3-O-(2,4,6-tri-O-benzyl-α-D-galactopyranosyl)-β-D-galactopyranoside吡啶三甲基溴硅烷茴香硫醚三氧化硫三氟乙酸 作用下, 以 甲醇N,N-二甲基甲酰胺 为溶剂, 反应 52.0h, 生成 3-(2-aminoethylthio)propyl 3-O-(3-O-sulfo-α-D-galactopyranosyl)-6-O-sulfo-β-D-galactopyranoside disodium salt
    参考文献:
    名称:
    Synthesis of a set of di- and tri-sulfated galabioses
    摘要:
    Among cell-adhesion molecules, L-selectin recognizes sulfated sLe(x) with relatively low affinity. Here, we aimed at artificial mimics by synthesizing a set of di- and tri-sulfated galabioses, which may surpass the affinity of sulfated sLe(x). As a strategy to obtain 3',6',6-tri-O-sulfogalabioses, regioselective reductive cleavage of 4,6- and 4',6'-di-O-benzylidenegalabioses was employed. Two suitably protected galactose precursors were conjugated to yield alpha and beta anomers (48 and 18%, respectively) by using a pentenyl galactoside donor and iodinium di-sym-collidine perchlorate as the catalyst. For synthesizing the 3',6-di-O-sulfogalabiose, however, a trichloroacetimidate donor was superior (52%) to the pentenyl one (30%). (C) 2001 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0008-6215(01)00222-1
  • 作为产物:
    参考文献:
    名称:
    Synthesis of a set of di- and tri-sulfated galabioses
    摘要:
    Among cell-adhesion molecules, L-selectin recognizes sulfated sLe(x) with relatively low affinity. Here, we aimed at artificial mimics by synthesizing a set of di- and tri-sulfated galabioses, which may surpass the affinity of sulfated sLe(x). As a strategy to obtain 3',6',6-tri-O-sulfogalabioses, regioselective reductive cleavage of 4,6- and 4',6'-di-O-benzylidenegalabioses was employed. Two suitably protected galactose precursors were conjugated to yield alpha and beta anomers (48 and 18%, respectively) by using a pentenyl galactoside donor and iodinium di-sym-collidine perchlorate as the catalyst. For synthesizing the 3',6-di-O-sulfogalabiose, however, a trichloroacetimidate donor was superior (52%) to the pentenyl one (30%). (C) 2001 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0008-6215(01)00222-1
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