3,9-二甲基-3,9-二氮杂双环[3.3.1]壬烷 | 3431-14-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪烷类
• 中文名称: 3,9-二甲基-3,9-二氮杂双环[3.3.1]壬烷
• 英文名称: 3,9-Dimethyl-3,9-diaza-bicyclo<3.3.1>nonan
• 英文别名: 3,9-Dimethyl-3,9-diazabicyclo[3.3.1]nonane
• CAS: 3431-14-9
• 化学式: C₉H₁₈N₂
• 分子量: 154.255
• InChiKey: GRVYLQCUQSTGMP-UHFFFAOYSA-N

物化性质

• 沸点：
  69 °C(Press: 7 Torr)
• 密度：
  0.947±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.1
• 重原子数：
  11
• 可旋转键数：
  0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  6.5
• 氢给体数：
  0
• 氢受体数：
  2

文献信息

• Methods for Treating Cognitive Disorders Using Inhibitors of Histone Deacetylase
  申请人：Forum Pharmaceuticals, Inc.

  公开号：US20170000749A1

  公开（公告）日：2017-01-05

  This disclosure relates to compounds for the inhibition of histone deacetylase and treatment of a cognitive disorder or deficit. More particularly, the disclosure provides for compounds of formula (I) wherein Q, J, L and Z are as defined in the specification.

  这份披露涉及用于抑制组蛋白去乙酰化酶和治疗认知障碍或缺陷的化合物。更具体地，该披露提供了公式（I）的化合物 其中 Q、J、L和Z如规范中所定义。
• DERIVATIVES OF (BRIDGED PIPERAZINYL)-1-ALKANONE AND USE THEREOF AS p75 INHIBITORS
  申请人：BARONI Marco

  公开号：US20110144116A1

  公开（公告）日：2011-06-16

  The present invention relates to derivatives of ((phenyl)-3,6-dihydropyridin-1-yl)(bridged piperazinyl)-1-alkanone derivatives and ((phenyl)-2,5-dihydropyrrol-1-yl) (bridged piperazinyl)-1-alkanone corresponding to Formula (I): in which the variables are as defined herein, to the preparation thereof and to the therapeutic use thereof.

  本发明涉及到((苯基)-3,6-二氢吡啶-1-基)(桥式哌嗪基)-1-烷酮衍生物和((苯基)-2,5-二氢吡咯-1-基)(桥式哌嗪基)-1-烷酮衍生物，对应于式(I)：其中变量如此处所定义，以及其制备和治疗用途。
• 5-HT3 RECEPTOR MODULATORS, METHODS OF MAKING, AND USE THEREOF
  申请人：Manning David D.

  公开号：US20090298809A1

  公开（公告）日：2009-12-03

  Novel 5-HT 3 receptor modulators are disclosed. These compounds are used in the treatment of various disorders, including chemotherapy-induced nausea and vomiting, post-operative nausea and vomiting, and irritable bowel syndrome. Methods of making these compounds are also described in the present invention.

  揭示了新型5-HT3受体调节剂。这些化合物用于治疗各种疾病，包括化疗诱发的恶心和呕吐、术后恶心和呕吐以及肠易激综合征。本发明还描述了制备这些化合物的方法。
• Inhibitors of Histone Deacetylase
  申请人：Deziel Robert

  公开号：US20080207590A1

  公开（公告）日：2008-08-28

  This invention relates to compounds for the inhibition of histone deacetylase. More particularly, the invention provides for compounds of formula (I) wherein Q, J, L and Z are as defined in the specification.

  该发明涉及用于抑制组蛋白去乙酰化酶的化合物。更具体地，该发明提供了式（I）中Q、J、L和Z所定义的化合物。
• Cyclic sulfones useful as mitochondrial sodium-calcium exchangers
  申请人：Bold Guido

  公开号：US20100029626A1

  公开（公告）日：2010-02-04

  The invention relates to novel compounds of formula (I) and their use in the treatment of the animal or human body, to pharmaceutical compositions comprising a compound of formula (I) and to the use of a compound of formula (I) for the preparation of pharmaceutical compositions for use in the treatment of protein kinase dependent diseases, especially of proliferative diseases, such as in particular tumour diseases.

  本发明涉及公式（I）的新化合物及其在动物或人体治疗中的应用，包括含有公式（I）化合物的制药组合物，以及使用公式（I）化合物制备用于治疗蛋白激酶依赖性疾病的制药组合物，特别是增殖性疾病，如特定的肿瘤疾病。