2-azidoethyl (methyl 2,3,4-tri-O-pivaloyl-β-D-glucopyranosyluronate)-(1-> 3)-4,6-di-O-acetyl-2-O-benzoyl-β-D-galactopyranosyl)-(1-> 4)-(2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranosyl)-(1-> 3)-(2,4,6-tri-O-benzyl-β-D-galactopyranosyl)... | 321746-73-0

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 2-azidoethyl (methyl 2,3,4-tri-O-pivaloyl-β-D-glucopyranosyluronate)-(1-> 3)-4,6-di-O-acetyl-2-O-benzoyl-β-D-galactopyranosyl)-(1-> 4)-(2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranosyl)-(1-> 3)-(2,4,6-tri-O-benzyl-β-D-galactopyranosyl)...
• CAS: 321746-73-0
• 化学式: C₁₁₇H₁₃₈N₄O₃₃
• 分子量: 2128.39
• InChiKey: WLKQKLPWZBHJPN-ZQMMPOJQSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  15.33
• 重原子数：
  154.0
• 可旋转键数：
  49.0
• 环数：
  14.0
• sp3杂化的碳原子比例：
  0.47
• 拓扑面积：
  428.1
• 氢给体数：
  1.0
• 氢受体数：
  34.0

反应信息

• 作为反应物：
  描述：

  2-azidoethyl (methyl 2,3,4-tri-O-pivaloyl-β-D-glucopyranosyluronate)-(1-> 3)-4,6-di-O-acetyl-2-O-benzoyl-β-D-galactopyranosyl)-(1-> 4)-(2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranosyl)-(1-> 3)-(2,4,6-tri-O-benzyl-β-D-galactopyranosyl)... 在 lithium hydroxide 作用下， 以 四氢呋喃 、 水 为溶剂， 生成
  参考文献：
  名称：

  Synthesis of 3-O-sulfoglucuronyl lacto-N-neotetraose 2-aminoethyl glycoside and biotinylated neoglycoconjugates thereof

  摘要：

  The 2-aminoethyl glycoside of pentasaccharide 3-O-sulfo-GlcA(beta -1 --> 3)Gal(beta -1 --> 4)GlcNAc(beta -1 --> 3)Gal(beta -1 --> 4)Glc(beta (1) and its conjugates with biotin and biotinylated polyacrylic acid were synthesized as molecular probes to investigate the recognition of the HNK-1 epitope containing carbohydrates by proteins. Key steps in the first of two investigated schemes for the preparation of the target compound 1 were (a) assembling of the pentasaccharide backbone (compound 10) by glycosylation of selectively substituted allyl glycoside of the trisaccharide GlcNAc(beta -1 --> 3)Gal(beta -1 --> 4)Glc(beta with glucuronyl-galactose glycosyl donor, (b) transformation of the allyl aglycon in 10 into 2-azidoethyl one (to give 11), (c) selective deprotection of the OH group at C-3 of the GlcA residue in 11 via saponification, intramolecular formation of 6,3-lacton (13) and its methanolysis, and (d) subsequent O-sulfation. The alternative scheme with the use of 2-azido-ethyl glycoside of the trisaccharide GlcNAc(beta -1 --> 3)Gal(beta -1 --> 4)Glc(beta instead of the allyl glycoside 6 was less effective due to smaller yield at the step of pentasaccharide synthesis. Additionally to 1 the 2-aminoethyl glycosides of the oligosaccharides GlcA(beta -1 --> 3)Gal(beta -1 --> 4)GlcNAc(beta -1 --> 3)Gal(beta -1 --> 4)Glc(beta, 3-O-sulfo-GlcA(beta -1 --> 3)Gal(beta, and GlcA(beta -1 --> 3)Gal(beta were also synthesized. (C) 2000 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0008-6215(00)00258-5
• 作为产物：
  描述：

  4,6-di-O-acetyl-2-O-benzoyl-3-O--α-D-galactopyranosyl trichloroacetimidate 、 2-azidoethyl (2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranosyl)-(1-> 3)-(2,4,6-tri-O-benzyl-β-D-galactopyranosyl)-(1-> 4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 在 三氟甲磺酸三甲基硅酯 、 4 A molecular sieve 作用下， 以 二氯甲烷 为溶剂， 反应 80.0h， 以62%的产率得到2-azidoethyl (methyl 2,3,4-tri-O-pivaloyl-β-D-glucopyranosyluronate)-(1-> 3)-4,6-di-O-acetyl-2-O-benzoyl-β-D-galactopyranosyl)-(1-> 4)-(2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranosyl)-(1-> 3)-(2,4,6-tri-O-benzyl-β-D-galactopyranosyl)...
  参考文献：
  名称：

  Synthesis of 3-O-sulfoglucuronyl lacto-N-neotetraose 2-aminoethyl glycoside and biotinylated neoglycoconjugates thereof

  摘要：

  The 2-aminoethyl glycoside of pentasaccharide 3-O-sulfo-GlcA(beta -1 --> 3)Gal(beta -1 --> 4)GlcNAc(beta -1 --> 3)Gal(beta -1 --> 4)Glc(beta (1) and its conjugates with biotin and biotinylated polyacrylic acid were synthesized as molecular probes to investigate the recognition of the HNK-1 epitope containing carbohydrates by proteins. Key steps in the first of two investigated schemes for the preparation of the target compound 1 were (a) assembling of the pentasaccharide backbone (compound 10) by glycosylation of selectively substituted allyl glycoside of the trisaccharide GlcNAc(beta -1 --> 3)Gal(beta -1 --> 4)Glc(beta with glucuronyl-galactose glycosyl donor, (b) transformation of the allyl aglycon in 10 into 2-azidoethyl one (to give 11), (c) selective deprotection of the OH group at C-3 of the GlcA residue in 11 via saponification, intramolecular formation of 6,3-lacton (13) and its methanolysis, and (d) subsequent O-sulfation. The alternative scheme with the use of 2-azido-ethyl glycoside of the trisaccharide GlcNAc(beta -1 --> 3)Gal(beta -1 --> 4)Glc(beta instead of the allyl glycoside 6 was less effective due to smaller yield at the step of pentasaccharide synthesis. Additionally to 1 the 2-aminoethyl glycosides of the oligosaccharides GlcA(beta -1 --> 3)Gal(beta -1 --> 4)GlcNAc(beta -1 --> 3)Gal(beta -1 --> 4)Glc(beta, 3-O-sulfo-GlcA(beta -1 --> 3)Gal(beta, and GlcA(beta -1 --> 3)Gal(beta were also synthesized. (C) 2000 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0008-6215(00)00258-5