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(2S)-2-amino-2-[1-[(2-amino-6-oxo-1H-purin-9-yl)methoxy]ethyl]-3-methylbutanoic acid

中文名称
——
中文别名
——
英文名称
(2S)-2-amino-2-[1-[(2-amino-6-oxo-1H-purin-9-yl)methoxy]ethyl]-3-methylbutanoic acid
英文别名
——
(2S)-2-amino-2-[1-[(2-amino-6-oxo-1H-purin-9-yl)methoxy]ethyl]-3-methylbutanoic acid化学式
CAS
——
化学式
C13H20N6O4
mdl
——
分子量
324.34
InChiKey
OHBMNVKWVFNEHN-GRSHUZJTSA-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):
    -2.4
  • 重原子数:
    23
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.54
  • 拓扑面积:
    158
  • 氢给体数:
    4
  • 氢受体数:
    6

文献信息

  • SUBSTITUTED METHYLFORMYL REAGENTS AND METHOD OF USING SAME TO MODIFY PHYSICOCHEMICAL AND/OR PHARMACOKINETIC PROPERTIES OF COMPOUNDS
    申请人:Dugar Sundeep
    公开号:US20140121367A1
    公开(公告)日:2014-05-01
    The present invention relates to the synthesis and application of novel chiral/achiral substituted methyl formyl reagents to modify pharmaceutical agents and/or biologically active substances to modify the physicochemical, biological and/or pharmacokinetic properties of the resulting compounds from the unmodified original agent.
    本发明涉及合成和应用新型手性/无手性取代甲基甲酰试剂来修饰药物和/或生物活性物质,以改变未经修饰的原始试剂的物理化学、生物学和/或药代动力学性质,从而得到改性后的化合物。
  • COMBINED SYSTEMIC AND TOPICAL TREATMENT OF DISORDERED TISSUES
    申请人:Quadex Pharmaceuticals, LLC
    公开号:EP2968228A1
    公开(公告)日:2016-01-20
  • TOPICAL APPLICATION FOR AN ANTI-HSV ANTIBODY
    申请人:Heidelberg ImmunoTherapeutics GmbH
    公开号:EP3160997A1
    公开(公告)日:2017-05-03
  • COMBINED SYSTEMIC AND TOPICAL TREATMENT OF DISORDERED AND/OR PRODROMAL STAGE TISSUE
    申请人:QUADEX PHARMACEUTICALS, LLC
    公开号:US20150374704A1
    公开(公告)日:2015-12-31
    Compositions and methods for treating disordered and/or prodromal stage tissue infected with by a virus in a mammal by co-administering a systemic anti-virus drug and topically administered anti-infective composition. The systemic anti-virus drug is internally administered and disrupts or inhibits virus replication systemically within the mammal. Examples include nucleoside analogues, nucleoside analogue precursors, and nucleotide analogues. The topically administered anti-infective composition includes at least one anti-infective agent, such as an organohalide (e.g., benzalkonium chloride), and is formulated to penetrate below the skin surface and allow the anti-infective agent to kill viruses at a treatment site. The topical anti-infective composition enhances efficacy of the systemic anti-virus drug and reduces the time and/or number of dosages otherwise required for the systemic anti-virus drug to treat the viral infection. The topical anti-infective composition can be more beneficial than the systemic anti-virus drug in killing viruses and can reduce or eliminate post-herpetic neuralgia.
  • US9359376B2
    申请人:——
    公开号:US9359376B2
    公开(公告)日:2016-06-07
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