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2-(4-{2-[2-cyclopentyl-5-[6-chloro-[1,2,4]triazolo[1,5-a]pyrimidin-2-ylmethyl]-4-hydroxy-6-oxo-3,6-dihydro-2H-pyran-2-yl]-ethyl}-2,6-difluoro-phenyl)-2-methyl-propionitrile | 749931-12-2

分子结构分类

中文名称
——
中文别名
——
英文名称
2-(4-{2-[2-cyclopentyl-5-[6-chloro-[1,2,4]triazolo[1,5-a]pyrimidin-2-ylmethyl]-4-hydroxy-6-oxo-3,6-dihydro-2H-pyran-2-yl]-ethyl}-2,6-difluoro-phenyl)-2-methyl-propionitrile
英文别名
2-[4-[2-[5-[(6-chloro-[1,2,4]triazolo[1,5-a]pyrimidin-2-yl)methyl]-2-cyclopentyl-4-hydroxy-6-oxo-3H-pyran-2-yl]ethyl]-2,6-difluorophenyl]-2-methylpropanenitrile
2-(4-{2-[2-cyclopentyl-5-[6-chloro-[1,2,4]triazolo[1,5-a]pyrimidin-2-ylmethyl]-4-hydroxy-6-oxo-3,6-dihydro-2H-pyran-2-yl]-ethyl}-2,6-difluoro-phenyl)-2-methyl-propionitrile化学式
CAS
749931-12-2
化学式
C28H28ClF2N5O3
mdl
——
分子量
556.012
InChiKey
ACQWOCBAUUSACB-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):
    5.6
  • 重原子数:
    39
  • 可旋转键数:
    7
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.46
  • 拓扑面积:
    113
  • 氢给体数:
    1
  • 氢受体数:
    9

文献信息

  • Inhibitors of hepatitis C virus RNA-dependent RNA polymerase, and compositions and treatments using the same
    申请人:Borchardt Allen
    公开号:US20050176701A1
    公开(公告)日:2005-08-11
    The invention relates to compounds of the formula 1 and to pharmaceutically acceptable salts, solvates, prodrugs and metabolites thereof, wherein W, Z, R 1 and R 2 , are as defined herein. The invention also relates to methods of treating Hepatitis C virus in mammals by administering the compounds of formula 1, and to pharmaceutical compositions for treating such disorders, which contain the compounds of formula 1. The invention also relates to methods of preparing the compounds of formula 1.
    这项发明涉及公式1的化合物,以及其药学上可接受的盐、溶剂化合物、前药和代谢物,其中W、Z、R1和R2如本文所定义。该发明还涉及通过给哺乳动物施用公式1的化合物来治疗丙型肝炎病毒的方法,以及用于治疗这类疾病的含有公式1化合物的药物组合物。该发明还涉及制备公式1化合物的方法。
  • Pharmaceutical compositions and methods for their use
    申请人:Agouron Pharmaceuticals, Inc.
    公开号:US20040224960A1
    公开(公告)日:2004-11-11
    The present invention relates to pharmaceutical compositions and to methods for their use in decreasing cytochrome P450 (CYP450) enzyme activity. The present invention also relates to methods of increasing the bioavailability of a compound in a mammal. Additionally, the present invention relates to methods of decreasing the metabolism of certain compounds in a mammal that are metabolized by the cytochrome P450 enzyme. Furthermore, the present invention relates to pharmaceutical compositions comprising at least one compound metabolized by at least one cytochrome P450 enzyme and a cytochrome P450 enzyme-inhibiting amount of a compound of formula (I).
    本发明涉及制药组合物及其在降低细胞色素P450(CYP450)酶活性方面的使用方法。本发明还涉及一种在哺乳动物中增加化合物生物利用度的方法。此外,本发明还涉及一种在哺乳动物中降低细胞色素P450酶代谢某些化合物的方法。此外,本发明还涉及包含至少一种由至少一种细胞色素P450酶代谢的化合物和公式(I)化合物的细胞色素P450酶抑制量的制药组合物。
  • INHIBITORS OF HEPATITIS C VIRUS RNA-DEPENDENT RNA POLYMERASE, AND COMPOSITIONS AND TREATMENTS USING THE SAME
    申请人:Borchardt Allen
    公开号:US20060189681A1
    公开(公告)日:2006-08-24
    The invention relates to compounds of the formula 1 and to pharmaceutically acceptable salts, solvates, prodrugs and metabolites thereof, wherein W, Z, R 1 and R 2 , are as defined herein. The invention also relates to methods of treating Hepatitis C virus in mammals by administering the compounds of formula 1, and to pharmaceutical compositions for treating such disorders, which contain the compounds of formula 1. The invention also relates to methods of preparing the compounds of formula 1.
    本发明涉及式1的化合物以及其药学上可接受的盐、溶剂合物、前药和代谢物,其中W、Z、R1和R2如本文所定义。本发明还涉及通过给哺乳动物投予式1的化合物来治疗丙型肝炎病毒的方法,以及包含式1的化合物的用于治疗此类疾病的制药组合物。本发明还涉及制备式1的化合物的方法。
  • US7148226B2
    申请人:——
    公开号:US7148226B2
    公开(公告)日:2006-12-12
  • US7473790B2
    申请人:——
    公开号:US7473790B2
    公开(公告)日:2009-01-06
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同类化合物

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