2-Isobutyl-6-methylpyrazin | 32184-48-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪类
• 英文名称: 2-Isobutyl-6-methylpyrazin
• 英文别名: 2-Methyl-6-isobutylpyrazin；2-isobutyl-6-methyl-pyrazine；2-Methyl-6-(2-methylpropyl)pyrazine
• CAS: 32184-48-8
• 化学式: C₉H₁₄N₂
• 分子量: 150.224
• InChiKey: LIRDEXCRJBABIY-UHFFFAOYSA-N

物化性质

• LogP：
  2.050 (est)
• 保留指数：
  1151.8

计算性质

• 辛醇/水分配系数(LogP)：
  1.8
• 重原子数：
  11
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.56
• 拓扑面积：
  25.8
• 氢给体数：
  0
• 氢受体数：
  2

文献信息

• Organic compounds
  申请人：Chowdhury Sultan

  公开号：US20090264444A1

  公开（公告）日：2009-10-22

  The present invention provides heterocyclic derivatives that modulate the activity of stearoyl-CoA desaturase. Methods of using such derivatives to modulate the activity of stearoyl-CoA desaturase and pharmaceutical compositions comprising such derivatives are also encompassed.

  本发明提供了调节硬脂酰辅酶A去饱和酶活性的杂环衍生物。本发明还涵盖了使用这些衍生物来调节硬脂酰辅酶A去饱和酶活性的方法和包含这些衍生物的制药组合物。
• SUBSTITUTED PYRIMIDINONES
  申请人：Durley C. Richard

  公开号：US20070167621A1

  公开（公告）日：2007-07-19

  Disclosed are compounds Formula I and pharmaceutically acceptable salts thereof, wherein R 1 , R 2 , R 4 , and R 5 are defined herein. These compounds are useful for treating diseases and conditions caused or exacerbated by unregulated p38 MAP Kinase and/or TNF activity. Pharmaceutical compositions containing the compounds, methods of preparing the compounds and methods of treatment using the compounds are also disclosed.

  本发明涉及化合物I的公式及其药学上可接受的盐，其中R1、R2、R4和R5在此定义。这些化合物可用于治疗由未经调节的p38 MAP激酶和/或TNF活性引起或恶化的疾病和病况。本发明还涉及含有这些化合物的药物组合物、制备这些化合物的方法以及使用这些化合物的治疗方法。
• ORGANIC COMPOUNDS
  申请人：Dales Natalie

  公开号：US20110105530A1

  公开（公告）日：2011-05-05

  The present invention provides heterocyclic derivatives that modulate the activity of stearoyl-CoA desaturase. Methods of using such derivatives to modulate the activity of stearoyl-CoA desaturase and pharmaceutical compositions comprising such derivatives are also encompassed.

  本发明提供了可以调节硬脂酰-辅酶A脱饱和酶活性的杂环衍生物。本发明还涵盖了使用这些衍生物来调节硬脂酰-辅酶A脱饱和酶活性的方法和包含这些衍生物的药物组合物。
• SPIRO DERIVATIVES FOR THE MODULATION OF STEAROYL-COA DESATURASE
  申请人：Dales Natalie

  公开号：US20120010135A1

  公开（公告）日：2012-01-12

  The present invention provides spiro derivatives that modulate the activity of stearoyl-CoA desaturase. Methods of using such derivatives to modulate the activity of stearoyl-CoA desaturase and pharmaceutical compositions comprising such derivatives are also encompassed.

  本发明提供了螺环衍生物，可以调节硬脂酰辅酶A脱饱和酶的活性。还包括使用这些衍生物调节硬脂酰辅酶A脱饱和酶的方法以及包含这些衍生物的制药组合物。
• PYRAZOLE DERIVATIVES WHICH MODULATE STEAROYL-COA DESATURASE
  申请人：Dales Natalie

  公开号：US20130011361A1

  公开（公告）日：2013-01-10

  The present invention provides heterocyclic derivatives of formula (I) that modulate the activity of stearoyl-CoA desaturase. Methods of using such derivatives to modulate the activity of stearoyl-CoA desaturase and pharmaceutical compositions comprising such derivatives are also encompassed.

  本发明提供了式（I）的杂环衍生物，其调节硬脂酰辅酶A去饱和酶的活性。还涵盖使用这些衍生物来调节硬脂酰辅酶A去饱和酶活性的方法，以及包含这些衍生物的制药组合物。