1-(biphenyl-4-ylmethyl)-2-butyl-1H-imidazo[4,5-c]quinolin-4-ylamine | 1258457-55-4

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 1-(biphenyl-4-ylmethyl)-2-butyl-1H-imidazo[4,5-c]quinolin-4-ylamine
• 英文别名: 1-(biphenyl-4-ylmethyl)-2-butyl-1H-imidazo[4,5-c]quinolin-4-amine；2-butyl-1-[(4-phenylphenyl)methyl]imidazo[4,5-c]quinolin-4-amine
• CAS: 1258457-55-4
• 化学式: C₂₇H₂₆N₄
• 分子量: 406.53
• InChiKey: UWRCUKBQVVLKLL-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.3
• 重原子数：
  31
• 可旋转键数：
  6
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.19
• 拓扑面积：
  56.7
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  在 氨 作用下， 以 甲醇 为溶剂， 生成 1-(biphenyl-4-ylmethyl)-2-butyl-1H-imidazo[4,5-c]quinolin-4-ylamine
  参考文献：
  名称：

  Syntheses of fluorescent imidazoquinoline conjugates as probes of Toll-like receptor 7

  摘要：

  Toll-like receptor (TLR)-7 agonists show prominent immunostimulatory activities. The synthesis of a TLR7-active N-1-(4-aminomethyl)benzyl substituted imidazoquinoline 5d served as a convenient precursor for the covalent attachment of fluorophores without significant loss of activity. Fluorescence microscopy experiments show that the fluorescent analogues are internalized and distributed in the endosomal compartment. Flow cytometry experiments using whole human blood show differential partitioning into B, T, and natural killer (NK) lymphocytic subsets, which correlate with the degree of activation in these subsets. These fluorescently-labeled imidazoquinolines will likely be useful in examining the trafficking of TLR7 in immunological synapses. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2010.09.093

文献信息

• TOLL-LIKE RECEPTOR-7 AND -8 MODULATORY 1H IMIDAZOQUINOLINE DERIVED COMPOUNDS
  申请人：David Sunil A.

  公开号：US20120294885A1

  公开（公告）日：2012-11-22

  The present disclosure provides novel imidazoquinoline derived compounds, derivatives thereof, analogues thereof, and pharmaceutically acceptable salts thereof, and methods of making and using such compounds. The present disclosure also provides TLR7 agonists and TLR7/TLR8 dual agonists, probes, tissue-specific molecules, adjuvants, immunogenic compositions, therapeutic compositions, and self-adjuvanting vaccines including the imidazoquinoline derived compounds, derivatives thereof, analogues thereof, and pharmaceutically acceptable salts thereof. Derivatives of the imidazoquinoline derived compounds also include dendrimers and dimers of the imidazoquinoline derived compounds, and methods of making and using the dendrimeic and dimeric imidazoquinoline derived compounds. The present disclosure also provides dual TLR2/TLR7 hybrid agonists that include imidazoquinoline derived compounds of the present disclosure.

  本公开提供了新型咪唑喹啉衍生化合物，其衍生物，类似物，以及其药用盐，并提供了制备和使用这些化合物的方法。本公开还提供了TLR7激动剂和TLR7/TLR8双激动剂，探针，组织特异性分子，佐剂，免疫原性组合物，治疗组合物，以及包括咪唑喹啉衍生化合物，其衍生物，类似物和药用盐的自佐剂疫苗。咪唑喹啉衍生化合物的衍生物还包括咪唑喹啉衍生化合物的树枝状分子和二聚体，以及制备和使用这些树枝状和二聚体咪唑喹啉衍生化合物的方法。本公开还提供了包括本公开的咪唑喹啉衍生化合物的双TLR2/TLR7混合激动剂。
• Toll-like receptor-7 and -8 modulatory 1H imidazoquinoline derived compounds
  申请人：The University of Kansas

  公开号：US10208037B2

  公开（公告）日：2019-02-19

  The present disclosure provides novel imidazoquinoline derived compounds, derivatives thereof, analogues thereof, and pharmaceutically acceptable salts thereof, and methods of making and using such compounds. The present disclosure also provides TLR7 agonists and TLR7/TLR8 dual agonists, probes, tissue-specific molecules, adjuvants, immunogenic compositions, therapeutic compositions, and self-adjuvanting vaccines including the imidazoquinoline derived compounds, derivatives thereof, analogues thereof, and pharmaceutically acceptable salts thereof. Derivatives of the imidazoquinoline derived compounds also include dendrimers and dimers of the imidazoquinoline derived compounds, and methods of making and using the dendrimeric and dimeric imidazoquinoline derived compounds. The present disclosure also provides dual TLR2/TLR7 hybrid agonists that include imidazoquinoline derived compounds of the present disclosure.

  本公开提供了新型咪唑喹啉衍生化合物、其衍生物、其类似物、其药学上可接受的盐，以及制造和使用此类化合物的方法。本公开还提供了 TLR7 激动剂和 TLR7/TLR8 双激动剂、探针、组织特异性分子、佐剂、免疫原性组合物、治疗组合物和自佐剂疫苗，包括咪唑喹啉衍生化合物、其衍生物、其类似物和其药学上可接受的盐。咪唑喹啉衍生化合物的衍生物还包括咪唑喹啉衍生化合物的树枝状分子和二聚体，以及树枝状和二聚体咪唑喹啉衍生化合物的制造和使用方法。本公开还提供了双重TLR2/TLR7混合激动剂，其中包括本公开的咪唑喹啉衍生化合物。
• US20140256922A1
  申请人：——

  公开号：US20140256922A1

  公开（公告）日：2014-09-11
• US8728486B2
  申请人：——

  公开号：US8728486B2

  公开（公告）日：2014-05-20
• US9441005B2
  申请人：——

  公开号：US9441005B2

  公开（公告）日：2016-09-13