N-[3-(1-butyryl-piperidin-4-ylsulfamoyl)-5,6,7,8-tetrahydro-naphthalen-1-yl]-2-chloro-benzamide | 723308-42-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 四氢化萘
• 英文名称: N-[3-(1-butyryl-piperidin-4-ylsulfamoyl)-5,6,7,8-tetrahydro-naphthalen-1-yl]-2-chloro-benzamide
• 英文别名: N-[3-[(1-butanoylpiperidin-4-yl)sulfamoyl]-5,6,7,8-tetrahydronaphthalen-1-yl]-2-chlorobenzamide
• CAS: 723308-42-7
• 化学式: C₂₆H₃₂ClN₃O₄S
• 分子量: 518.077
• InChiKey: UBNBWWILSHVVHV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.6
• 重原子数：
  35
• 可旋转键数：
  7
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.46
• 拓扑面积：
  104
• 氢给体数：
  2
• 氢受体数：
  5

文献信息

• [EN] CCR8 INHIBITORS<br/>[FR] INHIBITEURS DU CCR8
  申请人：MILLENNIUM PHARM INC

  公开号：WO2004058709A1

  公开（公告）日：2004-07-15

  Disclosed are CCR8 inhibitors represented by Structural Formulas (I). The variables in Structural Formula (I) are described herein. Also disclosed are methods of treating a subject with a CCR8 mediated condition, especially asthma, by administering one of the disclosed CCR8 inhibitors to the subject.

  揭示了由结构式（I）代表的CCR8抑制剂。结构式（I）中的变量在此处描述。还揭示了通过向受试者施用所披露的CCR8抑制剂之一来治疗CCR8介导的疾病，特别是哮喘的方法。
• Aryl sulfonamides useful as inhibitors of chemokine receptor activity
  申请人：Dai Mingshi

  公开号：US20050085518A1

  公开（公告）日：2005-04-21

  The present invention provides compounds of general formula I: or a pharmaceutically acceptable salt thereof, wherein R 1 , X, Z, R 2 , X., Ar, n, R 3 and R 4 are defined generally and in subsets herein. Compounds of the invention are inhibitors of CCR8 and accordingly are useful for the treatment of a variety of inflammatory and allergic disorders.

  本发明提供一般式I的化合物:或其药学上可接受的盐，其中R1、X、Z、R2、X.、Ar、n、R3和R4在本文中一般和子集中定义。本发明的化合物是CCR8的抑制剂，因此可用于治疗各种炎症和过敏性疾病。
• CCR8 Inhibitors
  申请人：Millennium Pharmaceuticals, Inc.

  公开号：US20040209948A1

  公开（公告）日：2004-10-21

  Disclosed are CCR8 inhibitors represented by Structural Formulas (I): 1 The variables in Structural Formula (I) are described herein. Also disclosed are methods of treating a subject with a CCR8 mediated condition, especially asthma, by administering one of the disclosed CCR8 inhibitors to the subject.

  本发明涉及由结构式（I）表示的CCR8抑制剂：1结构式（I）中的变量在此文中进行了描述。本发明还涉及通过向受试者给予所披露的CCR8抑制剂之一来治疗CCR8介导的疾病，特别是哮喘的方法。
• CCR8 INHIBITORS
  申请人：MILLENNIUM PHARMACEUTICALS, INC.

  公开号：EP1590327A1

  公开（公告）日：2005-11-02
• US7378525B2
  申请人：——

  公开号：US7378525B2

  公开（公告）日：2008-05-27