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5-[5-(4-Chlorophenyl)pent-4-ynyl]-5-(4-methoxyphenylsulfanyl)thiazolidine-2,4-dione | 500709-78-4

中文名称
——
中文别名
——
英文名称
5-[5-(4-Chlorophenyl)pent-4-ynyl]-5-(4-methoxyphenylsulfanyl)thiazolidine-2,4-dione
英文别名
5-[5-(4-Chlorophenyl)pent-4-ynyl]-5-(4-methoxyphenyl)sulfanyl-1,3-thiazolidine-2,4-dione
5-[5-(4-Chlorophenyl)pent-4-ynyl]-5-(4-methoxyphenylsulfanyl)thiazolidine-2,4-dione化学式
CAS
500709-78-4
化学式
C21H18ClNO3S2
mdl
——
分子量
431.964
InChiKey
YGZBGJDDWKXISM-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    5.9
  • 重原子数:
    28
  • 可旋转键数:
    7
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.24
  • 拓扑面积:
    106
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

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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.
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