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乙基2-氨基-5-羟基-1-甲基-6-氧代-1,6-二氢-4-嘧啶羧酸酯 | 729608-50-8

中文名称
乙基2-氨基-5-羟基-1-甲基-6-氧代-1,6-二氢-4-嘧啶羧酸酯
中文别名
——
英文名称
Ethyl 2-amino-5-hydroxy-1-methyl-6-oxo-1,6-dihydropyrimidine-4-carboxylate
英文别名
ethyl 2-amino-5-hydroxy-1-methyl-6-oxopyrimidine-4-carboxylate
乙基2-氨基-5-羟基-1-甲基-6-氧代-1,6-二氢-4-嘧啶羧酸酯化学式
CAS
729608-50-8
化学式
C8H11N3O4
mdl
——
分子量
213.19
InChiKey
WBLCUCXNMOHTPO-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):
    -0.3
  • 重原子数:
    15
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    105
  • 氢给体数:
    2
  • 氢受体数:
    5

文献信息

  • HIV integrase inhibitors
    申请人:——
    公开号:US20040204498A1
    公开(公告)日:2004-10-14
    Compounds useful for treating HIV are disclosed having the general formula 1 wherein R 1 , R 2 , and B are as defined in the specification. Compositions containing the compounds and methods for using the compounds to inhibit HIV are also disclosed.
    本发明揭示了用于治疗HIV的化合物,其具有以下一般式1,其中R1,R2和B在说明书中定义。还揭示了含有这些化合物的组合物以及使用这些化合物抑制HIV的方法。
  • THIADIAZOLE DERIVATIVES FOR THE TREATMENT OF NEURODEGENERATIVE DISEASES
    申请人:GRIFFIOEN Gerard
    公开号:US20090054410A1
    公开(公告)日:2009-02-26
    This invention provides specifically substituted 1,2,4-thiadiazole derivatives for use in the treatment of an α-synucleopathy such as Parkinson's disease, diffuse Lewy body disease, traumatic brain injury, amyotrophic lateral sclerosis, Niemann-Pick disease, Hallervorden-Spatz syndrome, Down syndrome, neuroaxonal dystrophy, multiple system atrophy and Alzheimer's disease. This invention also provides various methods for producing such substituted 1,2,4-thiadiazole derivatives.
  • US7135467B2
    申请人:——
    公开号:US7135467B2
    公开(公告)日:2006-11-14
  • US8541406B2
    申请人:——
    公开号:US8541406B2
    公开(公告)日:2013-09-24
  • [EN] HIV INTEGRASE INHIBITORS<br/>[FR] INHIBITEURS D'INTEGRASE HIV
    申请人:BRISTOL MYERS SQUIBB CO
    公开号:WO2004062613A2
    公开(公告)日:2004-07-29
    Compounds useful for treating HIV are disclosed having the general formula (I): wherein R1, R2, and B are as defined in the specification. Compositions containing the compounds and methods for using the compounds to inhibit HIV are also disclosed.
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