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methyl N-[(2S)-1-[(2S,3aS,7aS)-2-[6-[11-[2-[(2S,3aS,7aS)-1-[(2S)-3-cyano-2-(methoxycarbonylamino)propanoyl]-2,3,3a,4,5,6,7,7a-octahydroindol-2-yl]-3H-benzimidazol-5-yl]-5-tricyclo[8.2.2.24,7]hexadeca-1(12),4,6,10,13,15-hexaenyl]-1H-benzimidazol-2-yl]-2,3,3a,4,5,6,7,7a-octahydroindol-1-yl]-3-cyano-1-oxopropan-2-yl]carbamate | 1415120-10-3

中文名称
——
中文别名
——
英文名称
methyl N-[(2S)-1-[(2S,3aS,7aS)-2-[6-[11-[2-[(2S,3aS,7aS)-1-[(2S)-3-cyano-2-(methoxycarbonylamino)propanoyl]-2,3,3a,4,5,6,7,7a-octahydroindol-2-yl]-3H-benzimidazol-5-yl]-5-tricyclo[8.2.2.24,7]hexadeca-1(12),4,6,10,13,15-hexaenyl]-1H-benzimidazol-2-yl]-2,3,3a,4,5,6,7,7a-octahydroindol-1-yl]-3-cyano-1-oxopropan-2-yl]carbamate
英文别名
——
methyl N-[(2S)-1-[(2S,3aS,7aS)-2-[6-[11-[2-[(2S,3aS,7aS)-1-[(2S)-3-cyano-2-(methoxycarbonylamino)propanoyl]-2,3,3a,4,5,6,7,7a-octahydroindol-2-yl]-3H-benzimidazol-5-yl]-5-tricyclo[8.2.2.24,7]hexadeca-1(12),4,6,10,13,15-hexaenyl]-1H-benzimidazol-2-yl]-2,3,3a,4,5,6,7,7a-octahydroindol-1-yl]-3-cyano-1-oxopropan-2-yl]carbamate化学式
CAS
1415120-10-3
化学式
C58H62N10O6
mdl
——
分子量
995.194
InChiKey
GDBPQWFOYZHAJC-YBRUIIEASA-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):
    8.2
  • 重原子数:
    74
  • 可旋转键数:
    12
  • 环数:
    14.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    222
  • 氢给体数:
    4
  • 氢受体数:
    10

文献信息

  • SUBSITUTED ALIPHANES, CYCLOPHANES, HETERAPHANES, HETEROPHANES, HETERO-HETERAPHANES AND METALLOCENES USEFUL FOR TREATING HCV INFECTIONS
    申请人:Wiles Jason Allan
    公开号:US20120302538A1
    公开(公告)日:2012-11-29
    The present disclosure provides substituted aliphanes, cyclophanes, heteraphanes, heterophanes, hetero-heteraphanes and metallocenes, of Formula I D-M-D  (Formula I) useful as antiviral agents. In certain embodiments disclosed herein M is a group —P-A-P— where A is Certain substituted aliphanes, cyclophanes, heteraphanes, heterophanes, hetero-heteraphanes and metallocenes disclosed herein are potent and/or selective inhibitors of viral replication, particularly Hepatitis C virus replication. Pharmaceutical compositions/ and combinations containing one or more substituted aliphanes, cyclophanes, heteraphanes, heterophanes, hetero-heteraphanes and metallocenes and a pharmaceutically acceptable carrier are also provided by this disclosure. Methods for treating viral infections, including Hepatitis C viral infections are provided by the disclosure.
    本公开提供了替代脂环烷、环烷、杂环烷、杂脂环烷、杂杂环烷和属茂的化合物,其化学式为ID-M-D(化学式I),用作抗病毒剂。在本公开的某些实施例中,M是一个基团—P-A-P—,其中A是。本公开披露的某些替代脂环烷、环烷、杂环烷、杂脂环烷、杂杂环烷和属茂是病毒复制的有效和/或选择性抑制剂,特别是对乙型肝炎病毒复制。本公开还提供了含有一种或多种替代脂环烷、环烷、杂环烷、杂脂环烷、杂杂环烷和属茂以及药用载体的药物组合物/和配方。本公开提供了治疗病毒感染,包括乙型肝炎病毒感染的方法。
  • SUBSTITUTED ALIPHANES, CYCLOPHANES, HETERAPHANES, HETEROPHANES, HETERO-HETERAPHANES AND METALLOCENES USEFUL FOR TREATING HCV INFECTIONS
    申请人:Achillion Pharmaceuticals, Inc.
    公开号:US20180055824A1
    公开(公告)日:2018-03-01
    The present disclosure provides substituted aliphanes, cyclophanes, heteraphanes, heterophanes, hetero-heteraphanes and metallocenes, of Formula I D-M-D   (Formula I) useful as antiviral agents. In certain embodiments disclosed herein M is a group —P-A-P— where A is Certain substituted aliphanes, cyclophanes, heteraphanes, heterophanes, hetero-heteraphanes and metallocenes disclosed herein are potent and/or selective inhibitors of viral replication, particularly Hepatitis C virus replication. Pharmaceutical compositions/and combinations containing one or more substituted aliphanes, cyclophanes, heteraphanes, heterophanes, hetero-heteraphanes and metallocenes and a pharmaceutically acceptable carrier are also provided by this disclosure. Methods for treating viral infections, including Hepatitis C viral infections are provided by the disclosure.
    本公开提供了代替脂肪烷,环烷,杂环烷,杂环烷,杂-杂环烷和属茂的化合物,其化学式为ID-M-D(化学式I),可用作抗病毒剂。在本文中披露的某些实施例中,M是一个组- P-A-P-,其中A是某些代替脂肪烷,环烷,杂环烷,杂环烷,杂-杂环烷和属茂,是病毒复制的有效和/或选择性抑制剂,特别是丙型肝炎病毒复制的抑制剂。本公开还提供了含有一个或多个代替脂肪烷,环烷,杂环烷,杂环烷,杂-杂环烷和属茂以及药学上可接受的载体的制药组合物/和组合物。本公开还提供了用于治疗病毒感染,包括丙型肝炎病毒感染的方法。
  • INTERMEDIATES IN THE PREPARATION OF A BIS(BENZIMIDAZOLE)CYCLOPHANE DERIVATIVE
    申请人:Achillion Pharmaceuticals, Inc.
    公开号:EP3059241A1
    公开(公告)日:2016-08-24
    Provided is a compound having a structure selected from the group consisting of: which are intermediates in the preparation of Carbamic acid, N,N'-[tricyclo[8.2.2.24,7]hexadeca-4,6,10,12,13,15-hexaene-5,11-diyl bis [1H-benzimidazole-6,2-diyl[(2S,3aS,7aS)-octahydro-1H-indole-2,1-diyl][(1S)-1-(1-methylethyl)-2-oxo-2,1-ethane diyl]]] bis-, C,C'-dimethyl ester, which is a Hepatitis C virus NS5a (HCV NS5a) protease replication inhibitor
    本发明提供了一种化合物,其结构选自由以下组成的组: 是制备氨基甲酸的中间体、 N,N'-[三环[8.2.2.24,7]hexadeca-4,6,10,12,13,15-hexaene-5,11-diyl bis [1H-benzimidazole-6,2-diyl[(2S,3aS,7aS)-octahydro-1H-indole-2,1-diyl][(1S)-1-(1-methylethyl)-2-oxo-2,1-乙烷二基]]双 C,C'-二甲酯,它是一种丙型肝炎病毒 NS5a(HCV NS5a)蛋白酶复制抑制剂
  • US8809313B2
    申请人:——
    公开号:US8809313B2
    公开(公告)日:2014-08-19
  • US9273082B2
    申请人:——
    公开号:US9273082B2
    公开(公告)日:2016-03-01
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