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3,5-diamino-6-chloropyrazine-2-carboxylic acid [(R)-4-{3-[4-((S)-2,3-dihydroxypropoxy)phenyl]propyl}imidazolidin-(2Z)-ylidene]amide | 1160939-59-2

中文名称
——
中文别名
——
英文名称
3,5-diamino-6-chloropyrazine-2-carboxylic acid [(R)-4-{3-[4-((S)-2,3-dihydroxypropoxy)phenyl]propyl}imidazolidin-(2Z)-ylidene]amide
英文别名
(Z)-3,5-Diamino-6-chloro-N-((R)-4-(3-(4-((S)-2,3-dihydroxypropoxy)phenyl)propyl)imidazolidin-2-ylidene)pyrazine-2-carboxamide;3,5-diamino-6-chloro-N-[(5R)-5-[3-[4-[(2S)-2,3-dihydroxypropoxy]phenyl]propyl]-4,5-dihydro-1H-imidazol-2-yl]pyrazine-2-carboxamide
3,5-diamino-6-chloropyrazine-2-carboxylic acid [(R)-4-{3-[4-((S)-2,3-dihydroxypropoxy)phenyl]propyl}imidazolidin-(2Z)-ylidene]amide化学式
CAS
1160939-59-2
化学式
C20H26ClN7O4
mdl
——
分子量
463.924
InChiKey
RJZFOZKSHAJVLQ-OLZOCXBDSA-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

物化性质

  • 密度:
    1.58±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.9
  • 重原子数:
    32
  • 可旋转键数:
    10
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    181
  • 氢给体数:
    6
  • 氢受体数:
    9

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • COMPOSITIONS FOR TREATMENT OF CYSTIC FIBROSIS AND OTHER CHRONIC DISEASES
    申请人:Van Goor Fredrick F.
    公开号:US20110098311A1
    公开(公告)日:2011-04-28
    The present invention relates to pharmaceutical compositions comprising an inhibitor of epithelial sodium channel activity in combination with at least one ABC Transporter modulator compound of Formula A, Formula B, Formula C, or Formula D. The invention also relates to pharmaceutical formulations thereof, and to methods of using such compositions in the treatment of CFTR mediated diseases, particularly cystic fibrosis using the pharmaceutical combination compositions.
    本发明涉及包含上皮钠通道活性抑制剂与至少一种ABC转运蛋白调节剂化合物(A式、B式、C式或D式)的药物组合物。该发明还涉及这些药物配方,以及使用这些组合物治疗CFTR介导的疾病,特别是囊性纤维化的方法。
  • Organic Compounds
    申请人:BHALAY Gurdip
    公开号:US20100130506A1
    公开(公告)日:2010-05-27
    A compound of Formula I in free or salt or solvate form, where R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 and R 11 have the meanings as indicated in the specification, is useful for treating diseases which respond to the blockade of the epithelial sodium channel. Pharmaceutical compositions that contain the compounds and processes for preparing the compounds are also described.
    一种以自由形式、盐或溶剂形式存在的I式化合物,其中R1、R2、R3、R4、R5、R6、R7、R8、R9、R10和R11的含义如规范中所示,可用于治疗对上皮钠通道阻滞有反应的疾病。还描述了含有这些化合物的药物组合物以及制备这些化合物的方法。
  • Treating diseases mediated by blockade of the epithelial sodium channel with pyrazine-2-carboxamide derivatives
    申请人:Bhalay Gurpid
    公开号:US20110237572A1
    公开(公告)日:2011-09-29
    A compound of Formula I in free or salt or solvate form, where R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 and R 11 have the meanings as indicated in the specification, is useful for treating diseases which respond to the blockade of the epithelial sodium channel. Pharmaceutical compositions that contain the compounds and processes for preparing the compounds are also described.
    公式I的化合物以自由形式、盐形式或溶剂形式存在,其中R1、R2、R3、R4、R5、R6、R7、R8、R9、R10和R11的含义如说明书所示,可用于治疗对上皮钠通道阻滞有反应的疾病。还描述了包含该化合物的制药组合物和制备该化合物的过程。
  • Pyrazine-2-carboxamide derivatives to treat diseases mediated by blockade of the epithelial sodium channel
    申请人:Novartis AG
    公开号:US08039472B2
    公开(公告)日:2011-10-18
    A compound of Formula I in free or salt or solvate form, where R1, R2, R3, R4, R5, R6, R7, R8, R9, R10 and R11 have the meanings as indicated in the specification, is useful for treating diseases which respond to the blockade of the epithelial sodium channel. Pharmaceutical compositions that contain the compounds and processes for preparing the compounds are also described.
    公式I的化合物以自由形式、盐形式或溶剂化合物形式存在,其中R1、R2、R3、R4、R5、R6、R7、R8、R9、R10和R11的含义如规范中所示,可用于治疗对上皮钠通道阻滞有反应的疾病。还描述了含有这些化合物的制药组合物和制备这些化合物的方法。
  • ORGANIC COMPOUNDS
    申请人:BHALAY Gurdip
    公开号:US20130012500A1
    公开(公告)日:2013-01-10
    A compound of Formula I in free or salt or solvate form, where R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 and R 11 have the meanings as indicated in the specification, is useful for treating diseases which respond to the blockade of the epithelial sodium channel. Pharmaceutical compositions that contain the compounds and processes for preparing the compounds are also described.
    公式I的化合物以自由或盐或溶剂形式存在,其中R1、R2、R3、R4、R5、R6、R7、R8、R9、R10和R11的含义如规范中所示,可用于治疗对上皮钠通道阻滞作出反应的疾病。还描述了含有这些化合物的药物组合物和制备这些化合物的过程。
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