N-(cyclohexylmethyl)nicotinamide

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 英文名称: N-(cyclohexylmethyl)nicotinamide
• 英文别名: N-(cyclohexylmethyl)pyridine-3-carboxamide
• 化学式: C₁₃H₁₈N₂O
• 分子量: 218.29
• InChiKey: VFWYAQNRJZKZEN-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.3
• 重原子数：
  16
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.54
• 拓扑面积：
  42
• 氢给体数：
  1
• 氢受体数：
  2

文献信息

• Nicotinamide derivatives useful as p38 inhibitors
  申请人：Aston Mary Nicola

  公开号：US20050176964A1

  公开（公告）日：2005-08-11

  Compounds of formula (I): are inhibitors of p38 kinase and are useful in the treatment of conditions or disease states mediated by p38 kinase activity or mediated by cytokines produced by the activity of p38.

  式(I)的化合物是p38激酶的抑制剂，并且在治疗由p38激酶活性介导或由p38活性产生的细胞因子介导的疾病状态或条件中有用。
• Nicotinamide Derivatives Useful as p38 Inhibitors
  申请人：Aston Nicola

  公开号：US20060264479A1

  公开（公告）日：2006-11-23

  Compounds of formula (I): are inhibitors of p38 kinase and are useful in the treatment of conditions or disease states mediated by p38 kinase activity or mediated by cytokines produced by the activity of p38.

  式（I）的化合物是p38激酶的抑制剂，并且在治疗由p38激酶活性介导或由p38活性产生的细胞因子介导的疾病状态或条件中有用。
• NICOTINAMIDE DERIVATES USEFUL AS P38 INHIBITORS
  申请人：ASTON Nicola Mary

  公开号：US20100215652A1

  公开（公告）日：2010-08-26

  Compounds of formula (I): are inhibitors of p38 kinase and are useful in the treatment of conditions or disease states mediated by p38 kinase activity or mediated by cytokines produced by the activity of p38.

  化合物式（I）的化合物是p38激酶的抑制剂，并且在治疗由p38激酶活性介导或由p38活性产生的细胞因子介导的疾病状态或疾病状态中有用。
• Aromatic-Spiropiperidine oxazepinones (and thiones)
  申请人：A.H. ROBINS COMPANY, INCORPORATED (a Delaware corporation)

  公开号：EP0295833A1

  公开（公告）日：1988-12-21

  Novel aromatic-spiropiperidineoxazepinones and thiones exhibiting antihistamine activity are disclosed having the formula: wherein A represents an aromatic ring, selected from benzo when Z is carbon or pyrido[3,2-f] when Z is nitrogen either of which rings may be optionally substituted on carbon;     B is selected from oxygen or sulfur;     R¹ is selected from the group consisting of loweralkyl, cycloalkyl, cycloalkyl-loweralkyl or phenyl-loweralkyl of which phenyl may be optionally substituted;     R is selected from the group consisting of loweralkyl, cycloalkyl or phenyl-loweralkyl of which phenyl may be optionally substituted and the pharmaceutically acceptable salts thereof and novel chemical intermediates in the preparation thereof.

  本发明公开了具有抗组胺活性的新型芳香-硫代哌啶氧氮杂环庚酮和硫酮，其式如下 其中 A 代表芳香环，当 Z 为碳时，选自苯并环，当 Z 为氮时，选自吡啶并[3,2-f]环； B 选自氧或硫； R¹ 选自低烷基、环烷基、环烷基-低烷基或苯基-低烷基组成的组，其中苯基可被任选取代； R¹选自低级烷基、环烷基或苯基-低级烷基（其中苯基可被任选取代）组成的组，以及它们的药学上可接受的盐和制备它们的新型化学中间体。
• US7125898B2
  申请人：——

  公开号：US7125898B2

  公开（公告）日：2006-10-24