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O-(2-acetamido-2-desoxy-β-D-mannopyranosyl)-(1->4)-O-α-D-glucopyranosyl)-(1->3)1,2,4-tri-O-acetyl-α-L-rhamnopyranose | 118561-28-7

中文名称
——
中文别名
——
英文名称
O-(2-acetamido-2-desoxy-β-D-mannopyranosyl)-(1->4)-O-α-D-glucopyranosyl)-(1->3)1,2,4-tri-O-acetyl-α-L-rhamnopyranose
英文别名
O-(2-acetamide-2-deoxy-β-D-mannopyranosyl)-(1->4)-O-α-D-glucopyranosyl-(1->2)-β-L-rhamnopyranose;ManNAc(b1-4)Glc(a1-3)a-Rha;N-[(2S,3S,4R,5S,6R)-2-[(2R,3S,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(2R,3R,4R,5S,6S)-2,3,5-trihydroxy-6-methyloxan-4-yl]oxyoxan-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide
O-(2-acetamido-2-desoxy-β-D-mannopyranosyl)-(1->4)-O-α-D-glucopyranosyl)-(1->3)1,2,4-tri-O-acetyl-α-L-rhamnopyranose化学式
CAS
118561-28-7
化学式
C20H35NO15
mdl
——
分子量
529.496
InChiKey
JJVPWEKFORTMBV-XIRFQHHCSA-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):
    -5.8
  • 重原子数:
    36
  • 可旋转键数:
    7
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.95
  • 拓扑面积:
    257
  • 氢给体数:
    10
  • 氢受体数:
    15

反应信息

  • 作为产物:
    描述:
    3,4,6-tri-O-acetyl-2-azido-2-deoxy-α-D-mannopyranosyl bromide 在 palladium on activated charcoal 吡啶 、 2Ag(1+)*O4Si(2-) 、 4 A molecular sieve 、 硫化氢氢气sodium methylate溴化钛(IV)三氟乙酸 、 mercury dibromide 作用下, 以 吡啶甲醇二氯甲烷乙酸乙酯三乙胺甲苯 为溶剂, 反应 174.0h, 生成 O-(2-acetamido-2-desoxy-β-D-mannopyranosyl)-(1->4)-O-α-D-glucopyranosyl)-(1->3)1,2,4-tri-O-acetyl-α-L-rhamnopyranose
    参考文献:
    名称:
    从肺炎链球菌荚膜多糖合成三糖单元
    摘要:
    在硅酸银作为促进剂的存在下,2-叠氮基-2-脱氧-D-甘露糖的糖基溴化物与1,6-脱水-2,3-二-O-苄基-β-D-吡喃葡萄糖反应二糖β-D-ManpNac-(1 ---- 4)-D-Glcp的衍生物。衍生物被活化成二糖卤化物,并用作嵌段合成中的糖基供体。通过L-鼠李糖和D-葡萄糖的扩链,合成了四个三糖。它们代表各种肺炎链球菌类型的荚膜多糖“重复单元”的成分,β-D-Man-pNAc-(1 ---- 4)-alpha-D-Glcp-(1 ---- 2)-L- Rhap(19 F型),beta-D-ManpNAc-(1 ---- 4)-alpha-D-Glcp-(1 ---- 3)-L-Rhap(19 A型),beta-D- ManpNAc-(1 ---- 4)-alpha-D-Glcp-(1 ---- 4)-D-Glcp(9 A型)和beta-D-ManpNAc-(1 ---- 4) -beta-D-Glcp-(1
    DOI:
    10.1016/0008-6215(88)84117-x
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文献信息

  • An Alternative Access to a Trisaccharide Repeating Unit of the Capsular Polysaccharide of Streptococcus pneumoniae Serotype 19A.
    作者:Eisuke KAJI、Yumiko OSA、Mutsumi TANAIKE、Yugo HOSOKAWA、Hiroaki TAKAYANAGI、Atsushi TAKADA
    DOI:10.1248/cpb.44.437
    日期:——
    A chemical synthesis has been achieved for beta-D-ManNAc-(1-->4)-alpha-D-Glc-(1-->3)-L-Rha, a trisaccharide repeating unit of the capsular polysaccharide of Streptococcus pneumoniae serotype 19A, by stepwise link-up of the suitably functionalized, constituent sugar units. A beta-selective glycosylation of trimethylsilylethyl glucoside having free 4-OH with 2-(benzoyloxyimino)-2-deoxyglycosyl bromide
    化学合成已经实现了β-D-ManNAc-(1→4)-α-D-Glc-(1→3)-L-Rha,这是肺炎链球菌荚膜多糖的三糖重复单元。通过逐步连接适当官能化的糖单元,获得血清型19A。用2-(苯甲酰氧基亚氨基)-2-脱氧糖基溴化物将具有游离4-OH的三甲基甲硅烷基乙基葡糖苷进行β选择性糖基化,然后进行甘露聚糖选择性硼氢化,N-乙酰化和异头中心官能化(1-OSE-> 1 -OH-> 1-F),得到关键的二糖供体,β-D-ManNAc-(1-> 4)-alpha-D-Glc-(1-> F.L-鼠李糖基糖基化解封后,具有供体底物的受体受体在13步中从D-葡萄糖以6.5%的产率提供了目标三糖。
  • Synthese von trisaccharid-einheiten der kapselpolysaccharide von Streptococcus pneumoniae
    作者:Hans Paulsen、Bernd Helpap、Jens Peter Lorentzen
    DOI:10.1016/0008-6215(88)84117-x
    日期:1988.8
    beta-D-ManpNac-(1----4)-D- Glcp. The derivatives were activated into disaccharide halides and employed as glycosyl donors in block synthesis. By chain extension with L-rhamnose and D-glucose, four trisaccharides were synthesized. They represent components of capsular polysaccharide "repeating units" of various Streptococcus pneumoniae types, beta-D-Man-pNAc-(1----4)-alpha-D-Glcp-(1----2)-L-Rhap (type 19 F), beta
    在硅酸银作为促进剂的存在下,2-叠氮基-2-脱氧-D-甘露糖的糖基溴化物与1,6-脱水-2,3-二-O-苄基-β-D-吡喃葡萄糖反应二糖β-D-ManpNac-(1 ---- 4)-D-Glcp的衍生物。衍生物被活化成二糖卤化物,并用作嵌段合成中的糖基供体。通过L-鼠李糖和D-葡萄糖的扩链,合成了四个三糖。它们代表各种肺炎链球菌类型的荚膜多糖“重复单元”的成分,β-D-Man-pNAc-(1 ---- 4)-alpha-D-Glcp-(1 ---- 2)-L- Rhap(19 F型),beta-D-ManpNAc-(1 ---- 4)-alpha-D-Glcp-(1 ---- 3)-L-Rhap(19 A型),beta-D- ManpNAc-(1 ---- 4)-alpha-D-Glcp-(1 ---- 4)-D-Glcp(9 A型)和beta-D-ManpNAc-(1 ---- 4) -beta-D-Glcp-(1
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