(2R,3R,4R,5R,6S)-5-[4-(aminomethyl)triazol-1-yl]-2-(hydroxymethyl)-6-methyloxane-3,4-diol | 1355241-99-4

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (2R,3R,4R,5R,6S)-5-[4-(aminomethyl)triazol-1-yl]-2-(hydroxymethyl)-6-methyloxane-3,4-diol
• CAS: 1355241-99-4
• 化学式: C₁₀H₁₈N₄O₄
• 分子量: 258.277
• InChiKey: KMRNLWJPAHGCES-OQCUIOBLSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -2.7
• 重原子数：
  18
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.8
• 拓扑面积：
  127
• 氢给体数：
  4
• 氢受体数：
  7

反应信息

• 作为产物：
  描述：

  (2R,3R,4R)-2-(羟基甲基)-3,4-二氢-2H-吡喃-3,4-二醇 在 盐酸 、 三乙基硅烷 、 20% palladium hydroxide on charcoal 、 甲酸铵 、 双(三甲基硅烷基)氨基钾 、 sodium hydride 、 copper(II) sulfate 、 sodium ascorbate 、 pyridinium chlorochromate 作用下， 以 四氢呋喃 、 甲醇 、 乙醚 、 二氯甲烷 、 水 、 N,N-二甲基甲酰胺 、 甲苯 、 乙腈 为溶剂， 反应 32.91h， 生成 (2R,3R,4R,5R,6S)-5-[4-(aminomethyl)triazol-1-yl]-2-(hydroxymethyl)-6-methyloxane-3,4-diol
  参考文献：
  名称：

  Glycomimetic Ligands for the Human Asialoglycoprotein Receptor

  摘要：

  The asialoglycoprotein receptor (ASGPR) is a high-capacity galactose-binding receptor expressed on hepatocytes that binds its native substrates with low affinity. More potent ligands are of interest for hepatic delivery of therapeutic agents. We report several classes of galactosyl analogues with varied substitution at the anomeric, C2-, C5-, and C6-positions. Significant increases in binding affinity were noted for several trifluoromethyl-acetamide derivatives without covalent attachment to the protein. A variety of new ligands were obtained with affinity for ASGPR as good as or better than that of the parent N-acetylgalactosamine, showing that modification on either side of the key C3,C4-diol moiety is well tolerated, consistent with previous models of a shallow binding pocket. The galactosyl pyranose motif therefore offers many opportunities for the attachment of other functional units or payloads while retaining low-micromolar or better affinity for the ASGPR.

  DOI：

  10.1021/ja2104679

文献信息

• Glycomimetic Ligands for the Human Asialoglycoprotein Receptor
  作者：Sreeman K. Mamidyala、Sanjay Dutta、Boris A. Chrunyk、Cathy Préville、Hong Wang、Jane M. Withka、Alexander McColl、Timothy A. Subashi、Steven J. Hawrylik、Matthew C. Griffor、Sung Kim、Jeffrey A. Pfefferkorn、David A. Price、Elnaz Menhaji-Klotz、Vincent Mascitti、M.G. Finn

  DOI：10.1021/ja2104679

  日期：2012.2.1

  The asialoglycoprotein receptor (ASGPR) is a high-capacity galactose-binding receptor expressed on hepatocytes that binds its native substrates with low affinity. More potent ligands are of interest for hepatic delivery of therapeutic agents. We report several classes of galactosyl analogues with varied substitution at the anomeric, C2-, C5-, and C6-positions. Significant increases in binding affinity were noted for several trifluoromethyl-acetamide derivatives without covalent attachment to the protein. A variety of new ligands were obtained with affinity for ASGPR as good as or better than that of the parent N-acetylgalactosamine, showing that modification on either side of the key C3,C4-diol moiety is well tolerated, consistent with previous models of a shallow binding pocket. The galactosyl pyranose motif therefore offers many opportunities for the attachment of other functional units or payloads while retaining low-micromolar or better affinity for the ASGPR.