methyl 3-tert-butyldiphenylsilyl-(2R)-2-(6-O-acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranosyl)glycerate | 1096143-66-6

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: methyl 3-tert-butyldiphenylsilyl-(2R)-2-(6-O-acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranosyl)glycerate
• 英文别名: methyl 3-O-tert-butyldiphenylsilyl-(2R)-2-O-(6-O-acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-2,3-dihydroxypropanoate；methyl (2R)-2-[(2R,3R,4S,5R,6R)-6-(acetyloxymethyl)-3,4,5-tris(phenylmethoxy)oxan-2-yl]oxy-3-[tert-butyl(diphenyl)silyl]oxypropanoate
• CAS: 1096143-66-6
• 化学式: C₄₉H₅₆O₁₀Si
• 分子量: 833.063
• InChiKey: NRYKKOFDFURRGF-UCDSGCLNSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.17
• 重原子数：
  60
• 可旋转键数：
  22
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.35
• 拓扑面积：
  108
• 氢给体数：
  0
• 氢受体数：
  10

反应信息

• 作为反应物：
  描述：

  methyl 3-tert-butyldiphenylsilyl-(2R)-2-(6-O-acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranosyl)glycerate 在 甲醇 、 sodium 作用下， 反应 0.5h， 以94%的产率得到methyl 3-tert-butyldiphenylsilyl-(2R)-2-(2,3,4-tri-O-benzyl-α-D-glucopyranosyl)glycerate
  参考文献：
  名称：

  （2R）-2-O-α-d-吡喃葡萄糖基-（1-> 6）-α-d-吡喃葡萄糖基-2,3-二羟基丙酸钾的合成是天然的溶质。

  摘要：

  作为异构体的混合物，将乙基6-O-乙酰基-2,3,4-三苄基-1-硫代-d-吡喃葡萄糖苷用于（2R）-2-O-α-钾盐的立体选择性合成d-吡喃葡萄糖基-（1-> 6）-α-d-吡喃葡萄糖基-2,3-二羟基丙酸（α-d-葡萄糖基-（1-> 6）-alpha-d-葡萄糖基-（1-- > 2）-d-甘油酸（GGG），最近分离出的相容溶质。到目前为止，使用NIS / TfOH作为活化剂，α-端基异构体是两个糖基化反应的主要产物。

  DOI：

  10.1016/j.carres.2009.06.037
• 作为产物：
  描述：

  ethyl 6-O-acetyl-2,3,4-tri-O-benzyl-1-thio-α/β-D-glucopyranoside 、 (-)-methyl-(2R)-3-(tert-butyldiphenylsilyloxy)-2-hyrdoxypropanoate 在 2,6-二叔丁基-4-甲基吡啶 、 1-(苯基亚硫酰基)哌啶 、 三氟甲磺酸酐 作用下， 以 二氯甲烷 为溶剂， 反应 0.42h， 以76%的产率得到methyl 3-tert-butyldiphenylsilyl-(2R)-2-(6-O-acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranosyl)glycerate
  参考文献：
  名称：

  Design of new enzyme stabilizers inspired by glycosides of hyperthermophilic microorganisms

  摘要：

  In response to stressful conditions like supra-optimal salinity in the growth medium or temperature, many microorganisms accumulate low-molecular-mass organic compounds known as compatible solutes. In contrast with mesophiles that accumulate neutral or zwitterionic compounds, the solutes of hyperthermophiles are typically negatively charged. (2R)-2-(alpha-D-Mannopyranosyl)glycerate (herein abbreviated as mannosylglycerate) is one of the most widespread solutes among thermophilic and hyperthermophilic prokaryotes. In this work, several molecules chemically related to mannosylglycerate were namely (2S)-2-(1-O-alpha-D-mannopyranosyl)propionate, 2-(1-O-alpha-D-mannopyranosyl)acetate, synthesized, (2R)-2-(1-O-alpha-D-glucopyranosyl)glycerate and 1-O-(2-glyceryl)-alpha-D-mannopyraiioside. The effectiveness of the newly synthesized compounds for the protection of model enzymes against heat-induced denaturation, aggregation and inactivation was evaluated, using differential scanning calorimetry, light scattering and measurements of residual activity. For comparison, the protection induced by natural compatible solutes, either neutral (e.g., trehalose, glycerol, ectoine) or negatively charged (di-myo-inositol-1,3 '-phosphate and diglycerol phosphate), was assessed. Phosphate, sulfate, acetate and KCl were also included in the assays to rank the solutes and new compounds in the Hofmeister series. The data demonstrate the superiority of charged organic solutes as thermo-stabilizers of enzymes and strongly support the view that the extent of protein stabilization rendered by those solutes depends clearly on the specific solute/enzyme examined. The relevance of these findings to our knowledge on the mode of action of charged solutes is discussed. (C) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.carres.2008.08.030