methyl 4,6-O-benzylidene-3-deoxy-3-(4-methylbenzamido)-2-O-p-toluoyl-β-D-talopyranoside | 1346535-74-7

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: methyl 4,6-O-benzylidene-3-deoxy-3-(4-methylbenzamido)-2-O-p-toluoyl-β-D-talopyranoside
• CAS: 1346535-74-7
• 化学式: C₃₀H₃₁NO₇
• 分子量: 517.579
• InChiKey: LYNFLQJOEBUROT-KPBLPJOGSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.11
• 重原子数：
  38.0
• 可旋转键数：
  6.0
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  92.32
• 氢给体数：
  1.0
• 氢受体数：
  7.0

反应信息

• 作为反应物：
  描述：

  methyl 4,6-O-benzylidene-3-deoxy-3-(4-methylbenzamido)-2-O-p-toluoyl-β-D-talopyranoside 在 甲醇 、 水 、 sodium methylate 、 溶剂黄146 作用下， 反应 18.5h， 生成 methyl 3-deoxy-3-(4-methylbenzamido)-β-D-talopyranoside
  参考文献：
  名称：

  Synthesis of 3-amido-3-deoxy-β-d-talopyranosides: all-cis-substituted pyranosides as lectin inhibitors

  摘要：

  3-Deoxy-3-amino-beta-D-talopyranosides have been synthesized for the first time. The amines were obtained from galactopyranosides through 2,3-anhydrogulosides that were opened to idosides followed by an oxidation/reductive amination sequence. From the amines, 11 corresponding 3-deoxy-3-arylamido-beta-talopyranosides have been synthesized and evaluated as inhibitors against galectin-1, -2, -3, -4C, -4N, -7, -8N and -9N. The synthesized talosamides showed selectivity for Galectin-4C with three of the mono-saccharides having dissociation constants at around 100 mu M against the lectin, which is more than two orders of magnitude better than methyl beta-galactoside and significantly better than the previous best galectin-4C monosaccharide inhibitor. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2011.09.098
• 作为产物：
  描述：

  methyl 4,6-O-(S)-benzylidene-β-D-galactopyranoside 在 吡啶 、 potassium trimethylsilonate 、 ammonium acetate 、 水 、 sodium cyanoborohydride 、 戴斯-马丁氧化剂 、 potassium hydroxide 、 原甲酸三甲酯 作用下， 以 四氢呋喃 、 甲醇 、 二氯甲烷 、 N,N-二甲基甲酰胺 为溶剂， 反应 89.75h， 生成 methyl 4,6-O-benzylidene-3-deoxy-3-(4-methylbenzamido)-2-O-p-toluoyl-β-D-talopyranoside
  参考文献：
  名称：

  Synthesis of 3-amido-3-deoxy-β-d-talopyranosides: all-cis-substituted pyranosides as lectin inhibitors

  摘要：

  3-Deoxy-3-amino-beta-D-talopyranosides have been synthesized for the first time. The amines were obtained from galactopyranosides through 2,3-anhydrogulosides that were opened to idosides followed by an oxidation/reductive amination sequence. From the amines, 11 corresponding 3-deoxy-3-arylamido-beta-talopyranosides have been synthesized and evaluated as inhibitors against galectin-1, -2, -3, -4C, -4N, -7, -8N and -9N. The synthesized talosamides showed selectivity for Galectin-4C with three of the mono-saccharides having dissociation constants at around 100 mu M against the lectin, which is more than two orders of magnitude better than methyl beta-galactoside and significantly better than the previous best galectin-4C monosaccharide inhibitor. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2011.09.098