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[(3R,5S)-5-hydroxyoxan-3-yl]carbamic acid

中文名称
——
中文别名
——
英文名称
[(3R,5S)-5-hydroxyoxan-3-yl]carbamic acid
英文别名
——
[(3R,5S)-5-hydroxyoxan-3-yl]carbamic acid化学式
CAS
——
化学式
C6H11NO4
mdl
——
分子量
161.16
InChiKey
DZJBZDLDHRVLBK-UHNVWZDZSA-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):
    -0.9
  • 重原子数:
    11
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.83
  • 拓扑面积:
    78.8
  • 氢给体数:
    3
  • 氢受体数:
    4

文献信息

  • POLYCYCLIC-CARBAMOYLPYRIDONE COMPOUNDS AND THEIR PHARMACEUTICAL USE
    申请人:Gilead Sciences, Inc.
    公开号:US20140221356A1
    公开(公告)日:2014-08-07
    Compounds for use in the treatment of human immunodeficiency virus (HIV) infection are disclosed. The compounds have the following Formula (I): including stereoisomers and pharmaceutically acceptable salts thereof, wherein R 1 , X, W, Y 1 , Y 2 , Z 1 , and Z 4 are as defined herein. Methods associated with preparation and use of such compounds, as well as pharmaceutical compositions comprising such compounds, are also disclosed.
    本发明揭示了用于治疗人类免疫缺陷病毒(HIV)感染的化合物。这些化合物具有以下式子(I):包括立体异构体和其药学上可接受的盐,其中R1、X、W、Y1、Y2、Z1和Z4的定义如本文所述。本发明还揭示了与制备和使用这些化合物相关的方法,以及包含这些化合物的制药组合物。
  • SUBSTITUTED 1,2,3,4,6,8,12,12a-OCTAHYDRO-1,4-METHANODIPYRIDO[1,2-a:1',2'-d]PYRAZINES AND METHODS FOR TREATING VIRAL INFECTIONS
    申请人:Gilead Sciences, Inc.
    公开号:US20160176885A1
    公开(公告)日:2016-06-23
    Compounds for use in the treatment of human immunodeficiency virus (HIV) infection are disclosed. The compounds have the following Formula (I): including stereoisomers and pharmaceutically acceptable salts thereof, wherein R 1 , X, W, Y 1 , Y 2 , Z 1 , and Z 4 are as defined herein. Methods associated with preparation and use of such compounds, as well as pharmaceutical compositions comprising such compounds, are also disclosed.
    本发明揭示了用于治疗人类免疫缺陷病毒(HIV)感染的化合物。这些化合物具有以下式(I):包括立体异构体和其药学上可接受的盐,其中R1、X、W、Y1、Y2、Z1和Z4如本文所定义。本发明还揭示了与制备和使用这些化合物相关的方法,以及包含这些化合物的制药组合物。
  • Substituted 2,3,4,5,7,9,13,13a-octahydro-1,5-methanopyrido[1′,2′:4,5]pyrazino[1,2-a][1,3]diazepines and methods for treating viral infections
    申请人:Gilead Sciences, Inc.
    公开号:US10035809B2
    公开(公告)日:2018-07-31
    Compounds for use in the treatment of human immunodeficiency virus (HIV) infection are disclosed. The compounds have the following Formula (I): including stereoisomers and pharmaceutically acceptable salts thereof, wherein R1, X, W, Y1, Y2, Z1, and Z4 are as defined herein. Methods associated with preparation and use of such compounds, as well as pharmaceutical compositions comprising such compounds, are also disclosed.
    本研究公开了用于治疗人类免疫缺陷病毒(HIV)感染的化合物。这些化合物具有下式 (I): 包括其立体异构体和药学上可接受的盐类,其中 R1、X、W、Y1、Y2、Z1 和 Z4 如本文所定义。此外,还公开了与制备和使用此类化合物相关的方法,以及包含此类化合物的药物组合物。
  • Substituted 3,4,5,6,8,10,14,14a-octahydro-2h-2,6-methanopyrido[1′,2′:4,5]pyrazino[2,1-b][1,3]oxazocines and methods for treating viral infections
    申请人:Gilead Sciences, Inc.
    公开号:US10689399B2
    公开(公告)日:2020-06-23
    Compounds for use in the treatment of human immunodeficiency virus (HIV) infection are disclosed. The compounds have the following Formula (I): including stereoisomers and pharmaceutically acceptable salts thereof, wherein R1, X, W, Y1, Y2, Z1, and Z4 are as defined herein. Methods associated with preparation and use of such compounds, as well as pharmaceutical compositions comprising such compounds, are also disclosed.
    本研究公开了用于治疗人类免疫缺陷病毒(HIV)感染的化合物。这些化合物具有下式 (I): 包括其立体异构体和药学上可接受的盐类,其中 R1、X、W、Y1、Y2、Z1 和 Z4 如本文所定义。此外,还公开了与制备和使用此类化合物相关的方法,以及包含此类化合物的药物组合物。
  • SUBSTITUTED 2,3,4,5,7,9,13,13A-OCTAHYDRO-1,5-METHANOPYRIDO[1',2':4,5]PYRAZINO[1,3]DIAZEPINES AND METHODS FOR TREATING VIRAL INFECTIONS
    申请人:Gilead Sciences, Inc.
    公开号:US20190092787A1
    公开(公告)日:2019-03-28
    Compounds for use in the treatment of human immunodeficiency virus (HIV) infection are disclosed. The compounds have the following Formula (I): including stereoisomers and pharmaceutically acceptable salts thereof, wherein R 1 , X, W, Y 1 , Y 2 , Z 1 , and Z 4 are as defined herein. Methods associated with preparation and use of such compounds, as well as pharmaceutical compositions comprising such compounds, are also disclosed.
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