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2,2'-二氨基-2'-脱氧腺苷 | 215943-79-6

中文名称
2,2'-二氨基-2'-脱氧腺苷
中文别名
——
英文名称
2,2'-Diamino-2'-deoxyadenosine
英文别名
(2R,3S,4R,5R)-4-amino-5-(2,6-diaminopurin-9-yl)-2-(hydroxymethyl)oxolan-3-ol
2,2'-二氨基-2'-脱氧腺苷化学式
CAS
215943-79-6
化学式
C10H15N7O3
mdl
——
分子量
281.27
InChiKey
DIFJLWYUVQLAHS-DXTOWSMRSA-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:
    2.26
  • 溶解度:
    DMSO(稍微加热)

计算性质

  • 辛醇/水分配系数(LogP):
    -1.8
  • 重原子数:
    20
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    171
  • 氢给体数:
    5
  • 氢受体数:
    9

文献信息

  • 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
  • [EN] AMINO ACID PHOSPHORAMIDATE PRONUCLEOTIDES OF 2'-CYANO, AZIDO AND AMINO NUCLEOSIDES FOR THE TREATMENT OF HCV<br/>[FR] PRONUCLÉOTIDES DE PHOSPHORAMIDATE D'ACIDE AMINÉ DE 2'-CYANO, AZIDO ET AMINO NUCLÉOSIDES POUR LE TRAITEMENT DU VIRUS DE L'HÉPATITE C (VHC)
    申请人:IDENIX PHARMACEUTICALS INC
    公开号:WO2014160484A1
    公开(公告)日:2014-10-02
    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 or a pharmaceutically acceptable salt, solvate, stereoisomeric form, tautomeric form, or polymorphic form thereof, wherein Base, W, R1, R2, R10, and R11 are as described herein.
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