N-<6-(5-cholesten-3β-yloxy)hexyl>-N²-2,N⁶-bis<3-(α-D-mannopyranosylthio)propionyl>-L-lysyl>-N⁶-<3-(α-D-mannopyranosylthio)propionyl>-L-lysinamide | 79360-27-3

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 类固醇和类固醇衍生物
• 英文名称: N-<6-(5-cholesten-3β-yloxy)hexyl>-N²-2,N⁶-bis<3-(α-D-mannopyranosylthio)propionyl>-L-lysyl>-N⁶-<3-(α-D-mannopyranosylthio)propionyl>-L-lysinamide
• CAS: 79360-27-3
• 化学式: C₇₂H₁₂₅N₅O₂₁S₃
• 分子量: 1493.0
• InChiKey: UVZDCPUZTOYSIZ-QUZVXQBMSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  101.0
• 可旋转键数：
  42.0
• 环数：
  7.0
• sp3杂化的碳原子比例：
  0.9
• 拓扑面积：
  425.18
• 氢给体数：
  17.0
• 氢受体数：
  24.0

反应信息

• 作为产物：
  描述：

  N-<6-(5-cholesten-3β-yloxy)hexyl>-N²-2,N⁶-bis<3-<(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)thio>propionyl>-L-lysyl>-N⁶-<3-<(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)thio>propionyl>-L-lysinamide 在 水 、 三乙胺 作用下， 以 甲醇 为溶剂， 反应 2.0h， 以75%的产率得到N-<6-(5-cholesten-3β-yloxy)hexyl>-N²-2,N⁶-bis<3-(α-D-mannopyranosylthio)propionyl>-L-lysyl>-N⁶-<3-(α-D-mannopyranosylthio)propionyl>-L-lysinamide
  参考文献：
  名称：

  Cell-specific ligands for selective drug delivery to tissues and organs

  摘要：

  Various numbers of D-mannose residues have been attached via spacer arms to lysine, dilysine, and oligolysine backbones. These D-mannosyl peptide analogues were found to be potent competitive inhibitors of the uptake of 125I-labeled D-mannose-bovine serum albumin conjugate by rat alveolar macrophages. The inhibitory potency of these synthetic ligands increased with increasing number of carbohydrate moieties. The chirality of the peptide backbone did not appear to play a major role in binding, whereas variations of the length and linkage of the spacer arm notably affected the inhibitory activities. The saccharide specificity of the macrophage receptor was demonstrated by the inactivity of the corresponding D-galactosyl peptide analogues. The L-fucosyl peptide derivative was only weakly active. The trimannosyldilysine ligand (KI = 3.9 microM) and its analogues are potentially useful in selective delivery of therapeutic agents to macrophages.

  DOI：

  10.1021/jm00144a004