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(R)-4-(4-oxo-4,5-dihydro-thiazolo[4,5-d]pyridazin-2-yl)-1-(4-trifluoromethyl-benzenesulfonyl)-piperazine-2-carboxylic acid 4-trifluoromethoxy-benzylamide | 954388-83-1

中文名称
——
中文别名
——
英文名称
(R)-4-(4-oxo-4,5-dihydro-thiazolo[4,5-d]pyridazin-2-yl)-1-(4-trifluoromethyl-benzenesulfonyl)-piperazine-2-carboxylic acid 4-trifluoromethoxy-benzylamide
英文别名
(2R)-4-(4-oxo-5H-[1,3]thiazolo[4,5-d]pyridazin-2-yl)-N-[[4-(trifluoromethoxy)phenyl]methyl]-1-[4-(trifluoromethyl)phenyl]sulfonylpiperazine-2-carboxamide
(R)-4-(4-oxo-4,5-dihydro-thiazolo[4,5-d]pyridazin-2-yl)-1-(4-trifluoromethyl-benzenesulfonyl)-piperazine-2-carboxylic acid 4-trifluoromethoxy-benzylamide化学式
CAS
954388-83-1
化学式
C25H20F6N6O5S2
mdl
——
分子量
662.593
InChiKey
ACFIEVPCXWWMCM-GOSISDBHSA-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):
    4.4
  • 重原子数:
    44
  • 可旋转键数:
    7
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.28
  • 拓扑面积:
    170
  • 氢给体数:
    2
  • 氢受体数:
    16

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

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文献信息

  • Piperazine compound and use thereof as a HCV polymerase inhibitor
    申请人:Japan Tobacco Inc.
    公开号:US08017612B2
    公开(公告)日:2011-09-13
    The present invention relates to a compound represented by the following formula [I] wherein each symbol is as defined in the specification, or a pharmaceutically acceptable salt thereof, or a solvate thereof and an anti-HCV agent and an HCV polymerase inhibitor containing this compound. The compound of the present invention shows an anti-HCV activity based on the HCV polymerase inhibitory activity, and useful as an agent for the prophylaxis or treatment of hepatitis C.
    本发明涉及以下式[I]所表示的化合物,其中每个符号如规范中所定义,或其药学上可接受的盐,或其溶剂化物,以及含有该化合物的抗HCV剂和HCV聚合酶抑制剂。本发明的化合物基于HCV聚合酶抑制活性显示出抗HCV活性,并可用作预防或治疗丙型肝炎的药物。
  • NOVEL PIPERAZINE COMPOUND, AND USE THEREOF AS HCV POLYMERASE INHIBITOR
    申请人:Japan Tobacco, Inc.
    公开号:EP2009004A1
    公开(公告)日:2008-12-31
    The present invention relates to a compound represented by the following formula [I] wherein each symbol is as defined in the specification, or a pharmaceutically acceptable salt thereof, or a solvate thereof and an anti-HCV agent and an HCV polymerase inhibitor containing this compound. The compound of the present invention shows an anti-HCV activity based on the HCV polymerase inhibitory activity, and useful as an agent for the prophylaxis or treatment of hepatitis C.
    本发明涉及下式[I]所代表的化合物 其中各符号如说明书中所定义,或其药学上可接受的盐,或其溶液,以及含有该化合物的抗HCV药剂和HCV聚合酶抑制剂。本发明的化合物具有基于 HCV 聚合酶抑制活性的抗 HCV 活性,可用作丙型肝炎的预防或治疗剂。
  • US8017612B2
    申请人:——
    公开号:US8017612B2
    公开(公告)日:2011-09-13
  • New Piperazine Compound and Use Thereof as a HCV Polymerase Inhibitor
    申请人:Abe Hiroyuki
    公开号:US20080081818A1
    公开(公告)日:2008-04-03
    The present invention relates to a compound represented by the following formula [I] wherein each symbol is as defined in the specification, or a pharmaceutically acceptable salt thereof, or a solvate thereof and an anti-HCV agent and an HCV polymerase inhibitor containing this compound. The compound of the present invention shows an anti-HCV activity based on the HCV polymerase inhibitory activity, and useful as an agent for the prophylaxis or treatment of hepatitis C.
    本发明涉及一种由以下式[I]表示的化合物,其中每个符号如规范中定义,或其药学上可接受的盐,或其溶剂化合物,以及含有该化合物的抗HCV剂和HCV聚合酶抑制剂。本发明的化合物基于HCV聚合酶抑制活性显示出抗HCV活性,并且可用作预防或治疗丙型肝炎的药剂。
  • NEW PIPERAZINE COMPOUND AND USE THEREOF AS A HCV POLYMERASE INHIBITOR
    申请人:Abe Hiroyuki
    公开号:US20120107273A1
    公开(公告)日:2012-05-03
    The present invention relates to a compound represented by the following formula [I] wherein each symbol is as defined in the specification, or a pharmaceutically acceptable salt thereof, or a solvate thereof and an anti-HCV agent and an HCV polymerase inhibitor containing this compound. The compound of the present invention shows an anti-HCV activity based on the HCV polymerase inhibitory activity, and useful as an agent for the prophylaxis or treatment of hepatitis C.
    本发明涉及一种由下式[I]表示的化合物,其中每个符号如规范所定义,或其药学上可接受的盐,或其溶剂化物,以及含有该化合物的抗HCV剂和HCV聚合酶抑制剂。本发明的化合物基于HCV聚合酶抑制活性表现出抗HCV活性,可作为预防或治疗丙型肝炎的药剂。
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