5-[5-(2,5-Dichlorophenyl)-4-pentynyl]-5-{[5-(2-pyridinyl)-2-thienyl]sulfonyl}-1,3-thiazolidine-2,4-dione | 500710-89-4

• 分子结构分类: 有机化合物
• 英文名称: 5-[5-(2,5-Dichlorophenyl)-4-pentynyl]-5-{[5-(2-pyridinyl)-2-thienyl]sulfonyl}-1,3-thiazolidine-2,4-dione
• 英文别名: 5-[5-(2,5-Dichlorophenyl)-4-pentynyl]-5-{[5-(2-pyridinyl)-thien-2-yl]sulfonyl}-1,3-thiazolidine-2,4-dione；5-[5-(2,5-Dichlorophenyl)pent-4-ynyl]-5-(5-pyridin-2-ylthiophen-2-yl)sulfonyl-1,3-thiazolidine-2,4-dione
• CAS: 500710-89-4
• 化学式: C₂₃H₁₆Cl₂N₂O₄S₃
• 分子量: 551.495
• InChiKey: RKZMQOKIWHZNEZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.9
• 重原子数：
  34
• 可旋转键数：
  7
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.17
• 拓扑面积：
  155
• 氢给体数：
  1
• 氢受体数：
  7

文献信息

• Method of using 5-(arysulfonyl)-, 5-(arylsulfanyl)-and 5-(arylsulfanyl)thiazolidine-2,4-diones for inhibition of farnesyl-protein transferase
  申请人：American Cyanamid Company

  公开号：US20030144301A1

  公开（公告）日：2003-07-31

  This invention relates to a method of using novel 5-(arylsulfonyl)-, 5-(arylsulfinyl)- and 5-(arylsulfanyl)thiazolidine-2,4-diones of Formula (1), wherein Ar, Ar′, R 6 , m and n are as defined in the specification as inhibitors of Ras FPTase, and may be used as an alternative to, or in conjunction with, traditional cancer therapy for treating ras- oncogene-dependent tumors, such as cancers of the pancreas, colon, bladder, and thyroid. 1

  这项发明涉及使用新型5-(芳基磺酰基)-、5-(芳基亚砜基)-和5-(芳基硫基)噻唑烷-2,4-二酮的方法，其化学式如下(1)，其中Ar、Ar′、R6、m和n如规范中定义的作为Ras FPTase的抑制剂，并可作为传统癌症治疗的替代方案或与之结合，用于治疗Ras-致癌基因依赖性肿瘤，如胰腺癌、结肠癌、膀胱癌和甲状腺癌。
• 5-(arylsulfonyl)-,5-(arylsulfinyl), and 5-(arylsulfanyl)-thiazolidine-2,4-diones useful for inhibition of farnesyl-protein transferase
  申请人：American Cyanamid Company

  公开号：US20030149063A1

  公开（公告）日：2003-08-07

  This invention relates to a method of using novel 5-(arylsulfonyl)-,5- (arylsulfinyl), and 5-(arylsulfanyl)-thiazolidine-2,4-diones of Formula (I), wherein Ar, Ar′, R 6 , m and n are as defined in the specification as inhibitors of Ras FPTase, and may be used as an alternative to, or in conjunction with, traditional cancer therapy for treating ras- oncogene-dependent tumors, such as cancers of the pancreas, colon, bladder, and thyroid. 1

  本发明涉及一种使用新型5-(芳基磺酰基)-、5-(芳基亚磺酰基)和5-(芳基硫基)-噻唑烷-2,4-二酮（式（I）中的Ar、Ar'、R6、m和n如规范中定义）作为Ras FPTase抑制剂的方法，可用作替代传统癌症治疗或与之结合治疗ras-oncogene依赖性肿瘤，例如胰腺癌、结肠癌、膀胱癌和甲状腺癌。
• US6605628B1
  申请人：——

  公开号：US6605628B1

  公开（公告）日：2003-08-12
• US6784184B2
  申请人：——

  公开号：US6784184B2

  公开（公告）日：2004-08-31
• [EN] METHOD OF USING 5-(ARYLSULFONYL)-,5-(ARYLSULFINYL), AND 5-(ARYLSULFANYL)-THIAZOLIDINE-2,4-DIONES FOR INHIBITION OF FARNESYL-PROTEIN TRANSFERASE<br/>[FR] PROCEDE D'UTILISATION DE 5-(ARYLSULFONYLE)-,5-(ARYLSULFINYLE), ET 5-(ARYLSULFANYLE)-THIAZOLIDINE-2,4-DIONES POUR L'INHIBITION DE LA FARNESYLE-PROTEINE TRANSFERASE
  申请人：WYETH CORP

  公开号：WO2003018135A1

  公开（公告）日：2003-03-06

  This invention relates to novel 5-(arylsulfonyl)-thiazolidine-2,4-diones, and 5-(arylsulfanyl)-thiazolidine-2,4-diones of Formula (I), wherein Ar, Ar', R6, m and n are as defined in the specification as inhibitors of Ras FPTase, and may be used as an alternative to, or in conjunction with, traditional cancer therapy for treating ras-oncogene-dependent tumors, such as cancers of the pancreas, colon, bladder, and thyroid, to processes for the preparation of such compounds, and pharmaceutical compositions containing them.