benzyl 2,3-di-O-benzyl-6-deoxy-6-[2,3,5-tri-O-benzyl-1,4-dideoxy-1,4-episulfoniumylidene-D-arabinitol]-4-O-sulfoxy-β-D-glucopyranose inner salt | 878288-85-8

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: benzyl 2,3-di-O-benzyl-6-deoxy-6-[2,3,5-tri-O-benzyl-1,4-dideoxy-1,4-episulfoniumylidene-D-arabinitol]-4-O-sulfoxy-β-D-glucopyranose inner salt
• CAS: 878288-85-8
• 化学式: C₅₃H₅₆O₁₁S₂
• 分子量: 933.153
• InChiKey: STZIGTQZKKXIQQ-RLHQHUQESA-N

计算性质

• 辛醇/水分配系数(LogP)：
  8.33
• 重原子数：
  66.0
• 可旋转键数：
  23.0
• 环数：
  8.0
• sp3杂化的碳原子比例：
  0.32
• 拓扑面积：
  131.04
• 氢给体数：
  0.0
• 氢受体数：
  11.0

反应信息

• 作为反应物：
  描述：

  benzyl 2,3-di-O-benzyl-6-deoxy-6-[2,3,5-tri-O-benzyl-1,4-dideoxy-1,4-episulfoniumylidene-D-arabinitol]-4-O-sulfoxy-β-D-glucopyranose inner salt 在 palladium on activated charcoal 氢气 作用下， 以 甲醇 为溶剂， 20.0 ℃ 、101.32 kPa 条件下， 反应 22.0h， 生成 4-O-sulfoxy-6-deoxy-6-[1,4-dideoxy-1,4-episulfoniumylidene-D-arabinitol]-α-D-glucopyranose inner salt 、 4-O-sulfoxy-6-deoxy-6-[1,4-dideoxy-1,4-episulfoniumylidene-D-arabinitol]-β-D-glucopyranose inner salt
  参考文献：
  名称：

  Synthesis of Sulfonium Sulfate Analogues of Disaccharides and Their Conversion to Chain-Extended Homologues of Salacinol: New Glycosidase Inhibitors

  摘要：

  [graphics]Four chain extended homologues of salacinol, a naturally occurring glycosidase inhibitor, were prepared for evaluation as inhibitors of glucosidase enzymes involved in the breakdown of carbohydrates. The syntheses involved the reactions of 1,4-anhydro-2,3,5-tri-O-benzyl-4-thiO-D-arabinitol with cyclic sulfate derivatives of different monosaccharides. Debenzylation of the products afforded the novel sulfonium sulfate derivatives Of D-glucose, D-galactose, D-arabinose, and D-Xylose that are of interest in their own right as glycosidase inhibitors. Reduction to the corresponding alditols then afforded the homologues of salacinol containing polyhydroxylated, acyclic chains of 5- and 6-carbons, differing in stereochemistry at the stereogenic centers. Three of the chain-extended homologues inhibited recombinant human maltase glucoamylase, one of the key intestinal enzymes involved in the breakdown of glucose oligosaccharides in the sinall intestine, with K-i values in the low microinolar range, of approximately the saine inagnitude as salacinol, thus providing lead candidates for the treatment of Type 2 diabetes.

  DOI：

  10.1021/jo052252u
• 作为产物：
  描述：

  benzyl 2,3-di-O-benzyl-β-D-glucopyranoside 在 ruthenium trichloride 、 sodium periodate 、 氯化亚砜 、 六氟异丙醇 、 三乙胺 作用下， 以 四氯化碳 、 二氯甲烷 、 水 、 乙腈 为溶剂， 反应 42.58h， 生成 benzyl 2,3-di-O-benzyl-6-deoxy-6-[2,3,5-tri-O-benzyl-1,4-dideoxy-1,4-episulfoniumylidene-D-arabinitol]-4-O-sulfoxy-β-D-glucopyranose inner salt
  参考文献：
  名称：

  Synthesis of Sulfonium Sulfate Analogues of Disaccharides and Their Conversion to Chain-Extended Homologues of Salacinol: New Glycosidase Inhibitors

  摘要：

  [graphics]Four chain extended homologues of salacinol, a naturally occurring glycosidase inhibitor, were prepared for evaluation as inhibitors of glucosidase enzymes involved in the breakdown of carbohydrates. The syntheses involved the reactions of 1,4-anhydro-2,3,5-tri-O-benzyl-4-thiO-D-arabinitol with cyclic sulfate derivatives of different monosaccharides. Debenzylation of the products afforded the novel sulfonium sulfate derivatives Of D-glucose, D-galactose, D-arabinose, and D-Xylose that are of interest in their own right as glycosidase inhibitors. Reduction to the corresponding alditols then afforded the homologues of salacinol containing polyhydroxylated, acyclic chains of 5- and 6-carbons, differing in stereochemistry at the stereogenic centers. Three of the chain-extended homologues inhibited recombinant human maltase glucoamylase, one of the key intestinal enzymes involved in the breakdown of glucose oligosaccharides in the sinall intestine, with K-i values in the low microinolar range, of approximately the saine inagnitude as salacinol, thus providing lead candidates for the treatment of Type 2 diabetes.

  DOI：

  10.1021/jo052252u