摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

3-O-α-mannopyranosyl-α-D-mannopyranose | 50499-35-9

中文名称
——
中文别名
——
英文名称
3-O-α-mannopyranosyl-α-D-mannopyranose
英文别名
α-D-Man-(1->3)-α-D-Man;3α-mannobiose;α-Man-(1→3)-α-Man;α-(1-N3)-mannose disaccharide;mannobiose;3-O-alpha-D-mannopyranosyl-alpha-D-mannopyranose;(2S,3S,4S,5R,6R)-6-(hydroxymethyl)-4-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2,3,5-triol
3-O-α-mannopyranosyl-α-D-mannopyranose化学式
CAS
50499-35-9
化学式
C12H22O11
mdl
——
分子量
342.3
InChiKey
QIGJYVCQYDKYDW-LBGGPIGOSA-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):
    -4.2
  • 重原子数:
    23
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    190
  • 氢给体数:
    8
  • 氢受体数:
    11

反应信息

  • 作为反应物:
    描述:
    3-O-α-mannopyranosyl-α-D-mannopyranose乙酸酐吡啶 作用下, 生成 2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl-(1→3)-1,2,4,6-tetra-O-acetyl-α-D-mannopyranose
    参考文献:
    名称:
    通过快速原子轰击和电喷雾电离质谱法对类黄酮O-糖苷中的己糖和戊糖残基进行直接立体化学赋值。
    摘要:
    已经开发了质谱方法,其允许在黄酮类O-糖苷中末端单糖残基的直接立体化学分配,而无需化学水解。对含有葡萄糖,半乳糖,甘露糖,木糖,阿拉伯糖或apiose残基的标准品进行了检查,因为这些单糖是迄今为止在类黄酮糖苷中最常见的糖类。乙酰化之后,通过快速原子轰击(FAB)或电喷雾电离(ESI)产生的主要的过乙酰化糖相关片段,被选择为利用广泛的碰撞能量进行碰撞活化。事实证明,FAB和ESI都可用作电离技术。实现了立体选择性片段化,使我们能够清楚地区分和表征异构单糖残基。
    DOI:
    10.1002/jms.402
  • 作为产物:
    描述:
    3-O-acetyl-2,4,6-tri-O-benzyl-α-D-mannopyranosyl chloride 在 palladium on activated charcoal 4 A molecular sieve 、 氢气sodium methylatesilver trifluoromethanesulfonate 作用下, 以 四氢呋喃甲醇溶剂黄1461,2-二氯乙烷 为溶剂, 反应 55.0h, 生成 3-O-α-mannopyranosyl-α-D-mannopyranose
    参考文献:
    名称:
    Ogawa, Tomoya; Yamamoto, Hisao, Agricultural and Biological Chemistry, 1985, vol. 49, # 2, p. 475 - 482
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • A Novel Xylosylphosphotransferase Activity Discovered in Cryptococcus neoformans
    作者:Morgann C. Reilly、Steven B. Levery、Sherry A. Castle、J.Stacey Klutts、Tamara L. Doering
    DOI:10.1074/jbc.m109.056226
    日期:2009.12
    Cryptococcus neoformans is a fungal pathogen that causes serious disease in immunocompromised individuals. The organism produces a distinctive polysaccharide capsule that is necessary for its virulence, a predominantly polysaccharide cell wall, and a variety of protein- and lipid-linked glycans. The glycan synthetic pathways of this pathogen are of great interest. Here we report the detection of a novel glycosylphosphotransferase activity in C. neoformans, identification of the corresponding gene, and characterization of the encoded protein. The observed activity is specific for UDP-xylose as a donor and for mannose acceptors and forms a xylose-alpha-1-phosphate-6-mannose linkage. This is the first report of a xylosylphosphotransferase activity in any system.
  • Ogawa, Tomoya; Yamamoto, Hisao, Agricultural and Biological Chemistry, 1985, vol. 49, # 2, p. 475 - 482
    作者:Ogawa, Tomoya、Yamamoto, Hisao
    DOI:——
    日期:——
  • Direct stereochemical assignment of hexose and pentose residues in flavonoidO-glycosides by fast atom bombardment and electrospray ionization mass spectrometry
    作者:Filip Cuyckens、Abdelaaty A. Shahat、Luc Pieters、Magda Claeys
    DOI:10.1002/jms.402
    日期:2002.12
    Mass spectrometric methods have been developed which allow the direct stereochemical assignment of terminal monosaccharide residues in flavonoid O-glycosides without the need for chemical hydrolysis. Standards containing a glucose, galactose, mannose, xylose, arabinose or apiose residue were examined because these monosaccharides are by far the most commonly encountered in flavonoid glycosides. Following
    已经开发了质谱方法,其允许在黄酮类O-糖苷中末端单糖残基的直接立体化学分配,而无需化学水解。对含有葡萄糖,半乳糖,甘露糖,木糖,阿拉伯糖或apiose残基的标准品进行了检查,因为这些单糖是迄今为止在类黄酮糖苷中最常见的糖类。乙酰化之后,通过快速原子轰击(FAB)或电喷雾电离(ESI)产生的主要的过乙酰化糖相关片段,被选择为利用广泛的碰撞能量进行碰撞活化。事实证明,FAB和ESI都可用作电离技术。实现了立体选择性片段化,使我们能够清楚地区分和表征异构单糖残基。
查看更多