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(methyl 2,3,4-tri-O-benzyl-6-deoxy-α-D-galactopyranosid-6'-yl)-(methyl 2',3',4'-tri-O-benzyl-6'-deoxy-α-D-mannopyranosid-6-yl) sulfide | 1261294-48-7

中文名称
——
中文别名
——
英文名称
(methyl 2,3,4-tri-O-benzyl-6-deoxy-α-D-galactopyranosid-6'-yl)-(methyl 2',3',4'-tri-O-benzyl-6'-deoxy-α-D-mannopyranosid-6-yl) sulfide
英文别名
(2S,3R,4S,5R,6S)-2-methoxy-6-[[(2S,3S,4S,5S,6S)-6-methoxy-3,4,5-tris(phenylmethoxy)oxan-2-yl]methylsulfanylmethyl]-3,4,5-tris(phenylmethoxy)oxane
(methyl 2,3,4-tri-O-benzyl-6-deoxy-α-D-galactopyranosid-6'-yl)-(methyl 2',3',4'-tri-O-benzyl-6'-deoxy-α-D-mannopyranosid-6-yl) sulfide化学式
CAS
1261294-48-7
化学式
C56H62O10S
mdl
——
分子量
927.168
InChiKey
GRNGKIHDKPOWOY-VTVLSGBBSA-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):
    8.8
  • 重原子数:
    67
  • 可旋转键数:
    24
  • 环数:
    8.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    118
  • 氢给体数:
    0
  • 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
  • 下游产品
    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:
    (methyl 2,3,4-tri-O-benzyl-6-deoxy-α-D-galactopyranosid-6'-yl)-(methyl 2',3',4'-tri-O-benzyl-6'-deoxy-α-D-mannopyranosid-6-yl) sulfide间氯过氧苯甲酸 作用下, 以 二氯甲烷 为溶剂, 以80%的产率得到(methyl 2,3,4-tri-O-benzyl-6-deoxy-α-D-galactopyranosid-6-yl)-(methyl 2',3',4'-tri-O-benzyl-6'-deoxy-α-D-mannopyranosid-6'-yl) sulfone
    参考文献:
    名称:
    Efficient synthesis of (6-deoxy-glycopyranosid-6-yl) sulfone derivatives and their effect on Ca2+-ATPase
    摘要:
    Synthesis of a series of novel (6-deoxy-glycopyranosid-6-yl) sulfone derivatives has been achieved using a general synthetic strategy. Yields were excellent in every case. The synthetic compounds were evaluated for their biological potential against Ca2+-ATPase, an important enzyme involves in tranporting Ca2+ across the cell membranes. (C) 2010 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2010.09.069
  • 作为产物:
    描述:
    methyl 2,3,4-tri-O-benzyl-6-thio-6-S-acetyl-α-D-mannopyranoside 、 (2S,3R,4S,5R)-3,4,5-tris(benzyloxy)-2-(iodomethyl)-6-methoxytetrahydro-2H-pyran 在 sodium hydroxide 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 3.0h, 以83%的产率得到(methyl 2,3,4-tri-O-benzyl-6-deoxy-α-D-galactopyranosid-6'-yl)-(methyl 2',3',4'-tri-O-benzyl-6'-deoxy-α-D-mannopyranosid-6-yl) sulfide
    参考文献:
    名称:
    Efficient synthesis of (6-deoxy-glycopyranosid-6-yl) sulfone derivatives and their effect on Ca2+-ATPase
    摘要:
    Synthesis of a series of novel (6-deoxy-glycopyranosid-6-yl) sulfone derivatives has been achieved using a general synthetic strategy. Yields were excellent in every case. The synthetic compounds were evaluated for their biological potential against Ca2+-ATPase, an important enzyme involves in tranporting Ca2+ across the cell membranes. (C) 2010 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2010.09.069
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文献信息

  • Efficient synthesis of (6-deoxy-glycopyranosid-6-yl) sulfone derivatives and their effect on Ca2+-ATPase
    作者:Chinmoy Mukherjee、Swatilekha Ghosh、Pinki Nandi、Parimal C. Sen、Anup Kumar Misra
    DOI:10.1016/j.ejmech.2010.09.069
    日期:2010.12
    Synthesis of a series of novel (6-deoxy-glycopyranosid-6-yl) sulfone derivatives has been achieved using a general synthetic strategy. Yields were excellent in every case. The synthetic compounds were evaluated for their biological potential against Ca2+-ATPase, an important enzyme involves in tranporting Ca2+ across the cell membranes. (C) 2010 Elsevier Masson SAS. All rights reserved.
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