5-(piperidin-1-yl)methyl-2-(3-(piperidin-1-yl)propoxy)pyridine

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 5-(piperidin-1-yl)methyl-2-(3-(piperidin-1-yl)propoxy)pyridine
• 英文别名: 5-Piperidin-1-ylmethyl-2-(3-piperidin-1-yl-propoxy)-pyridine；5-(piperidin-1-ylmethyl)-2-(3-piperidin-1-ylpropoxy)pyridine
• 化学式: C₁₉H₃₁N₃O
• 分子量: 317.475
• InChiKey: MJFRUZWZLAZUGG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.1
• 重原子数：
  23
• 可旋转键数：
  7
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.74
• 拓扑面积：
  28.6
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  2-溴-5-(哌啶-1-基甲基)吡啶 在 sodium hydride 作用下， 以 DMF (N,N-dimethyl-formamide) 为溶剂， 反应 18.5h， 生成 5-(piperidin-1-yl)methyl-2-(3-(piperidin-1-yl)propoxy)pyridine
  参考文献：
  名称：

  Non-Imidazole heterocyclic compounds

  摘要：

  某些非咪唑杂环化合物是组胺H3调节剂，可用于治疗组胺H3受体介导的疾病。

  公开号：

  US20050222151A1

文献信息

• Isoxazole Compounds as Histamine H3 modulators
  申请人：Carruthers Nicholas I.

  公开号：US20100022539A1

  公开（公告）日：2010-01-28

  Certain isoxazole compounds are histamine H 3 modulators useful in the treatment of histamine H 3 receptor mediated diseases.

  某些异唑啉化合物是组胺H3调节剂，可用于治疗组胺H3受体介导的疾病。
• NON-IMIDAZOLE HETEROCYCLIC COMPOUNDS
  申请人：Carruthers Nicholas I.

  公开号：US20080306066A1

  公开（公告）日：2008-12-11

  Certain non-imidazole heterocyclic compounds are histamine H 3 modulators useful in the treatment of histamine H 3 receptor mediated diseases.

  某些非咪唑杂环化合物是组胺H3调节剂，可用于治疗组胺H3受体介导的疾病。
• Pyridine compounds as histamine H3 modulators
  申请人：Janssen Pharmaceutical, N.V.

  公开号：US07423147B2

  公开（公告）日：2008-09-09

  Certain non-imidazole heterocyclic compounds are Histamine H3 modulators in the treatment of Histamine H3 receptor mediated diseases.

  某些非咪唑杂环化合物是组胺H3受体调节剂，用于治疗组胺H3受体介导的疾病。
• Heterocyclic replacement of the central phenyl core of diamine-based histamine H3 receptor antagonists
  作者：Devin M. Swanson、Chandra R. Shah、Brian Lord、Kirsten Morton、Lisa K. Dvorak、Curt Mazur、Richard Apodaca、Wei Xiao、Jamin D. Boggs、Mark Feinstein

  DOI：10.1016/j.ejmech.2009.06.007

  日期：2009.11

  A series of small molecules consisting of a heterocyclic core flanked by two basic functionalities were synthesized and screened for in vitro affinity at the human histamine H-3 receptor (hH(3)R). Nine of the twenty-eight compounds tested were found to possess a hH(3)R K-i of less than 5 nM and consisted of a diverse range of central hetero-aromatic linkers (pyridine, pyrazine, oxazole, isoxazole, thiazole, furan, thiophene, and pyrrole). One member of this series, (4-isopropyl-piperazin-1-yl)-(6-piperidin-1-ylmethyl-pyridin-3-yl)-methanone (37), was found to be a high affinity, selective antagonist that crosses the blood-brain barrier and occupies H-3 receptors after oral administration in the rat. (C) 2009 Elsevier Masson SAS. All rights reserved.
• NON-IMIDAZOLE HETEROCYCLIC COMPOUNDS AS HISTAMINE H3-RECEPTOR LIGANDS
  申请人：JANSSEN PHARMACEUTICA N.V.

  公开号：EP1761496A2

  公开（公告）日：2007-03-14