2-[(4-Chlorophenoxy)methyl]pyridine | 16173-72-1

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: 2-[(4-Chlorophenoxy)methyl]pyridine
• CAS: 16173-72-1
• 化学式: C₁₂H₁₀ClNO
• 分子量: 219.671
• InChiKey: HUTBSWDISPHEGZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3
• 重原子数：
  15
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.08
• 拓扑面积：
  22.1
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  2-氯甲基吡啶盐酸盐 、 sodium 4-chlorophenolate 在 sodium ethanolate 作用下， 以 乙醇 为溶剂， 生成 2-[(4-Chlorophenoxy)methyl]pyridine
  参考文献：
  名称：

  2-[（（苯硫基）甲基]吡啶衍生物：新型抗炎药。

  摘要：

  2-[（（苯硫基）甲基]吡啶衍生物可抑制大鼠皮肤逆向被动Arthus反应（RPAR）。在同一模型中，消炎痛是无活性的，氢化可的松是有活性的。化合物Ia-d还显着减少了胸膜RPAR中的渗出液量和白细胞积聚。这种活性模式与氢化可的松相似，与消炎痛不同。

  DOI：

  10.1021/jm00356a018

文献信息

• PYRIDONE COMPOUND, AND AGRICULTURAL AND HORTICULTURAL FUNGICIDE HAVING THIS AS ACTIVE COMPONENT
  申请人：Mitsui Chemicals Agro, Inc.

  公开号：EP3611164A1

  公开（公告）日：2020-02-19

  Novel compounds controlling plant diseases are provided. Pyridone compounds of the invention are novel and can control plant diseases. The pyridone compounds of the invention encompass compounds of formula (1) and salts thereof.

  本发明提供了控制植物病害的新型化合物。本发明的吡啶酮化合物很新颖，可以控制植物病害。本发明的吡啶酮化合物包括式（1）化合物及其盐类。
• NOVEL PYRIDOPYRIMIDINONE COMPOUNDS FOR MODULATING THE CATALYTIC ACTIVITY OF HISTONE LYSINE DEMETHYLASES (KDMS)
  申请人：Dong-A ST Co., Ltd.

  公开号：EP3212647A2

  公开（公告）日：2017-09-06
• [EN] NOVEL PYRIDOPYRIMIDINONE COMPOUNDS FOR MODULATING THE CATALYTIC ACTIVITY OF HISTONE LYSINE DEMETHYLASES (KDMS)<br/>[FR] NOUVEAUX COMPOSÉS DE PYRIDOPYRIMIDINONE POUR MODULER L'ACTIVITÉ CATALYTIQUE DES HISTONE LYSINE DÉMÉTHYLASES (KDM)
  申请人：DONG A SOCIO HOLDINGS CO LTD

  公开号：WO2016068580A2

  公开（公告）日：2016-05-06

  The present invention provides a compound of Formula (I) being capable of modulating the activity of histone lysine demethylase (KDM), pharmaceutical compositions thereof, methods to prepare the said compounds, and the use of such compounds as a medicament. The compound of Formula (I) acts as KDM inhibitor with marked potency, thereby having an outstanding potential for a pharmaceutical intervention of cancer and any other diseases related to KDM dysregulation.
• 2-[(Phenylthio)methyl]pyridine derivatives: new antiinflammatory agents
  作者：Fortuna Haviv、Robert W. DeNet、Raymond J. Michaels、James D. Ratajczyk、George W. Carter、Patrick R. Young

  DOI：10.1021/jm00356a018

  日期：1983.2

  2-[(Phenylthio)methyl]pyridine derivatives inhibited the dermal reverse passive Arthus reaction (RPAR) in the rat. In the same model, indomethacin was inactive, and hydrocortisone was active. Compounds Ia-d also significantly reduced exudate volume and white blood cell accumulation in the pleural RPAR. This pattern of activity was similar to that of hydrocortisone and different from that of indomethacin

  2-[（（苯硫基）甲基]吡啶衍生物可抑制大鼠皮肤逆向被动Arthus反应（RPAR）。在同一模型中，消炎痛是无活性的，氢化可的松是有活性的。化合物Ia-d还显着减少了胸膜RPAR中的渗出液量和白细胞积聚。这种活性模式与氢化可的松相似，与消炎痛不同。