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[[(2R,3S,4R,5R)-5-(4-amino-2-oxopyrimidin-1-yl)-4-cyano-3-hydroxy-4-methyloxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate | 1491023-69-8

中文名称
——
中文别名
——
英文名称
[[(2R,3S,4R,5R)-5-(4-amino-2-oxopyrimidin-1-yl)-4-cyano-3-hydroxy-4-methyloxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate
英文别名
——
[[(2R,3S,4R,5R)-5-(4-amino-2-oxopyrimidin-1-yl)-4-cyano-3-hydroxy-4-methyloxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate化学式
CAS
1491023-69-8
化学式
C11H17N4O13P3
mdl
——
分子量
506.196
InChiKey
FJBRRNQDMWILIB-PNHWDRBUSA-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):
    -5.2
  • 重原子数:
    31
  • 可旋转键数:
    8
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.55
  • 拓扑面积:
    272
  • 氢给体数:
    6
  • 氢受体数:
    14

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

  • [EN] 2 -ALKYNYL SUBSTITUTED NUCLEOSIDE DERIVATIVES FOR TREATING VIRAL DISEASES<br/>[FR] DÉRIVÉS DE NUCLÉOSIDE À SUBSTITUTION ALKYNYLE EN POSITION 2 POUR LE TRAITEMENT DE MALADIES VIRALES
    申请人:MERCK SHARP & DOHME
    公开号:WO2014078463A1
    公开(公告)日:2014-05-22
    The present invention relates to 2'-Alkynyl Substituted Nucleoside Derivatives of Formula (I): and pharmaceutically acceptable salts thereof, wherein B, X, R1, R2, R3 and R4 are as defined herein. The present invention also relates to compositions comprising at least one 2'-Alkynyl Substituted Nucleoside Derivative, and methods of using the 2'-Alkynyl Substituted Nucleoside Derivatives for treating or preventing HCV infection in a patient.
    本发明涉及具有以下结构式(I)的2'-炔基取代核苷衍生物及其药用可接受的盐,其中B、X、R1、R2、R3和R4如本文所定义。本发明还涉及包含至少一种2'-炔基取代核苷衍生物的组合物,以及使用这些2'-炔基取代核苷衍生物治疗或预防患者HCV感染的方法。
  • AMINO ACID PHOSPHORAMIDATE PRONUCLEOTIDES OF 2'-CYANO, AZIDO AND AMINO NUCLEOSIDES FOR THE TREATMENT OF HCV
    申请人:Centre National De La Recherche Scientifique
    公开号:US20160113956A1
    公开(公告)日:2016-04-28
    Provided herein are compounds, compositions and methods for the treatment of Flaviviridae infections, including HCV infections. In certain embodiments, compounds and compositions of nucleoside derivatives are disclosed, which can be administered either alone or in combination with other anti-viral agents. In certain embodiments, the compounds are 2′-cyano, azido or amino nucleosides according to Formula 1001 or 2001: or a pharmaceutically acceptable salt, solvate, stereoisomeric form, tautomeric form, or polymorphic form thereof, wherein Base, W, R 1 and R 2 are as described herein.
    本文提供了治疗黄病毒科感染,包括丙型肝炎(HCV)感染的化合物、组合物和方法。在某些实施例中,揭示了核苷衍生物的化合物和组合物,可以单独或与其他抗病毒药物联合使用。在某些实施例中,所述化合物是根据公式1001或2001的2'-氰基,偶氮基或氨基核苷衍生物,或其药学上可接受的盐,溶剂化合物,立体异构体,互变异构体或多态形式,其中Base,W,R1和R2如本文所述。
  • Amino acid phosphoramidate pronucleotides of 2′-cyano, azido and amino nucleosides for the treatment of HCV
    申请人:Centre National De La Recherche Scientifique
    公开号:US10231986B2
    公开(公告)日:2019-03-19
    Provided herein are compounds, compositions and methods for the treatment of Flaviviridae infections, including HCV infections. In certain embodiments, compounds and compositions of nucleoside derivatives are disclosed, which can be administered either alone or in combination with other anti-viral agents. In certain embodiments, the compounds are 2′-cyano, azido or amino nucleosides according to Formula 1001 or 2001: or a pharmaceutically acceptable salt, solvate, stereoisomeric form, tautomeric form, or polymorphic form thereof, wherein Base, W, R1 and R2 are as described herein.
    本文提供了用于治疗黄病毒科感染(包括 HCV 感染)的化合物、组合物和方法。在某些实施方案中,公开了核苷衍生物的化合物和组合物,可单独使用或与其他抗病毒药物联合使用。在某些实施方案中,化合物是根据式 1001 或 2001 的 2′-氰基、叠氮或氨基核苷: 或其药学上可接受的盐、溶液、立体异构体、同分异构体或多晶型,其中碱、W、R1 和 R2 如本文所述。
  • US20140271547A1
    申请人:——
    公开号:US20140271547A1
    公开(公告)日:2014-09-18
  • 2'-ALKYNYL SUBSTITUTED NUCLEOSIDE DERIVATIVES AND METHODS OF USE THEREOF FOR THE TREATMENT OF VIRAL DISEASES
    申请人:BENNETT Frank
    公开号:US20150299243A1
    公开(公告)日:2015-10-22
    The present invention relates to 2′-Alkynyl Substituted Nucleoside Derivatives of Formula (I): and pharmaceutically acceptable salts thereof, wherein B, X, R1, R2, R3 and R4 are as defined herein. The present invention also relates to compositions comprising at least one 2′-Alkynyl Substituted Nucleoside Derivative, and methods of using the 2′-Alkynyl Substituted Nucleoside Derivatives for treating or preventing HCV infection in a patient.
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