| 187173-25-7

• 分子结构分类: 有机化合物 - 有机氧化合物
• CAS: 187173-25-7
• 化学式: C₃₁H₅₅IN₂O₁₆
• 分子量: 838.686
• InChiKey: JGURAZGXNNPZCH-SJSZWMRJSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -2.83
• 重原子数：
  50.0
• 可旋转键数：
  19.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.94
• 拓扑面积：
  264.42
• 氢给体数：
  9.0
• 氢受体数：
  16.0

反应信息

• 作为反应物：
  描述：

  苯硫酚 、 在 碳酸氢钠 作用下， 以 乙醇 为溶剂， 反应 1.0h， 以79%的产率得到
  参考文献：
  名称：

  New synthetic trisaccharide inhibitors for N-acetylglucosaminyltransferase-V

  摘要：

  The trisaccharide octyl 2-acetamido-2-deoxy-beta-D-glucopyranosyl-(1-->2)-alpha-D-mannopyranosyl-(1-->6)-beta-D-glucopyranoside (5) is an acceptor substrate for N-acetylglucosaminyltransferase-V (EC 2.4.1.155) which adds a beta-GlcNAc residue to OH-6 of the central Man-residue. In the present work, 10 analogues of 5, each missing the potentially reactive OH-6 group, were chemically synthesized. The key intermediate used was octyl 2-acetamido-2-deoxy-beta-D-glucopyranosyl-(1-->2)-6-amino-6-deoxy-4-O-methyl-alpha-D-mannopyranosyl-(1-->6)-beta-D-glucopyranoside (6a), which was synthesized in stepwise fashion by sequential coupling of protected monosaccharide residues. The 6'-amino group in 6a, was then selectively derivatized by either acylation or alkylation with hydrophobic, hydrophilic, charged, aromatic and potential covalently inactivating groups. The 10 trisaccharide analogues thus produced were evaluated for inhibition against GlcNAcT-V isolated from hamster kidney. All of the compounds were competitive inhibitors with K-i values ranging from 21 to 297 mu M. These results indicate that acceptor substrate (or inhibitor)-enzyme complex does not involve critical recognition contacts at the position of transfer. Copyright (C) 1996 Elsevier Science Ltd

  DOI：

  10.1016/s0968-0896(96)00180-0
• 作为产物：
  描述：

  4-pentenyl 2-O-benzoyl-3-O-benzyl-4-O-methyl-α-D-mannopyranoside 在 palladium on activated charcoal 吡啶 、 2,3,5-三甲基吡啶 、 盐酸 、 N-碘代丁二酰亚胺 、 sodium azide 、 4 A molecular sieve 、 氢气 、 sodium methylate 、 silver trifluoromethanesulfonate 、 乙二胺 、 三乙胺 作用下， 以 甲醇 、 乙醇 、 二氯甲烷 、 N,N-二甲基甲酰胺 、 正丁醇 为溶剂， -40.0~70.0 ℃ 、101.33 kPa 条件下， 反应 205.0h， 生成
  参考文献：
  名称：

  New synthetic trisaccharide inhibitors for N-acetylglucosaminyltransferase-V

  摘要：

  The trisaccharide octyl 2-acetamido-2-deoxy-beta-D-glucopyranosyl-(1-->2)-alpha-D-mannopyranosyl-(1-->6)-beta-D-glucopyranoside (5) is an acceptor substrate for N-acetylglucosaminyltransferase-V (EC 2.4.1.155) which adds a beta-GlcNAc residue to OH-6 of the central Man-residue. In the present work, 10 analogues of 5, each missing the potentially reactive OH-6 group, were chemically synthesized. The key intermediate used was octyl 2-acetamido-2-deoxy-beta-D-glucopyranosyl-(1-->2)-6-amino-6-deoxy-4-O-methyl-alpha-D-mannopyranosyl-(1-->6)-beta-D-glucopyranoside (6a), which was synthesized in stepwise fashion by sequential coupling of protected monosaccharide residues. The 6'-amino group in 6a, was then selectively derivatized by either acylation or alkylation with hydrophobic, hydrophilic, charged, aromatic and potential covalently inactivating groups. The 10 trisaccharide analogues thus produced were evaluated for inhibition against GlcNAcT-V isolated from hamster kidney. All of the compounds were competitive inhibitors with K-i values ranging from 21 to 297 mu M. These results indicate that acceptor substrate (or inhibitor)-enzyme complex does not involve critical recognition contacts at the position of transfer. Copyright (C) 1996 Elsevier Science Ltd

  DOI：

  10.1016/s0968-0896(96)00180-0