1-[2-(2-Chloro-4-methylphenoxy)ethyl]pyrrolidine

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: 1-[2-(2-Chloro-4-methylphenoxy)ethyl]pyrrolidine
• 化学式: C₁₃H₁₈ClNO
• 分子量: 239.74
• InChiKey: ANOOCTJKHQFBMI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  16
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.54
• 拓扑面积：
  12.5
• 氢给体数：
  0
• 氢受体数：
  2

文献信息

• POLYCYCLIC HETEROARYL SUBSTITUTED TRIAZOLES USEFUL AS AXL INHIBITORS
  申请人：RIGEL PHARMACEUTICALS, INC.

  公开号：US20140323490A1

  公开（公告）日：2014-10-30

  Polycyclic heteroaryl substituted triazoles and pharmaceutical compositions containing the compounds are disclosed as being useful in inhibiting the activity of the receptor protein tyrosine kinase Axl. Methods of using the compounds in treating diseases or conditions associated with Axl activity are also disclosed.

  本发明涉及多环杂芳基取代的三唑化合物以及含有这些化合物的制药组合物，这些化合物被揭示为在抑制受体蛋白酪氨酸激酶Axl的活性方面有用。还揭示了使用这些化合物治疗与Axl活性相关的疾病或病状的方法。
• DIAMINOTHIAZOLES USEFUL AS AXL INHIBITORS
  申请人：Goff Dane

  公开号：US20080227789A1

  公开（公告）日：2008-09-18

  Diaminothiazoles and pharmaceutical compositions containing them are disclosed as being useful in inhibiting the activity of the receptor protein tyrosine kinase Axl. Methods of using the diaminothiazoles in treating diseases or conditions associated with Axl activity are also disclosed.

  本发明揭示了二氨基噻唑类化合物和含有它们的药物组合物，作为抑制受体蛋白酪氨酸激酶Axl活性的有用药物。还揭示了使用二氨基噻唑类化合物治疗与Axl活性相关的疾病或病症的方法。
• Bisarylurea derivatives
  申请人：Buchstaller Hans-Peter

  公开号：US20070161677A1

  公开（公告）日：2007-07-12

  The present invention relates to bisarylurea derivatives of formula (I), the use of the compounds of formula (I) as inhibitors of raf-kinase, the use of the compounds of formula (I) for the manufacture of a pharmaceutical composition and a method of treatment, comprising administering said pharmaceutical composition to a patient.
• US7879856B2
  申请人：——

  公开号：US7879856B2

  公开（公告）日：2011-02-01
• US8288382B2
  申请人：——

  公开号：US8288382B2

  公开（公告）日：2012-10-16