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Isopropyl-(1-hydroxy-pentyl)-keton | 22612-64-2

中文名称
——
中文别名
——
英文名称
Isopropyl-(1-hydroxy-pentyl)-keton
英文别名
1-(1-hydroxy-cyclopentyl)-2-methyl-propan-1-one;1-(1-Hydroxy-cyclopentyl)-2-methyl-propan-1-on;1-(1-Hydroxycyclopentyl)-2-methylpropan-1-one
Isopropyl-(1-hydroxy-pentyl)-keton化学式
CAS
22612-64-2
化学式
C9H16O2
mdl
——
分子量
156.225
InChiKey
UQKVPLZXMYDNEO-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):
    1.4
  • 重原子数:
    11
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.89
  • 拓扑面积:
    37.3
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    Isopropyl-(1-hydroxy-pentyl)-keton氢氧化钾乙醚 作用下, 生成 2-hydroxy-2-isopropyl-cyclohexanone
    参考文献:
    名称:
    Elphimoff-Felkin et al., Bulletin de la Societe Chimique de France, 1958, p. 522,530
    摘要:
    DOI:
  • 作为产物:
    描述:
    alkaline earth salt of/the/ methylsulfuric acid 在 作用下, 生成 Isopropyl-(1-hydroxy-pentyl)-keton
    参考文献:
    名称:
    Elphimoff-Felkin et al., Bulletin de la Societe Chimique de France, 1958, p. 522,530
    摘要:
    DOI:
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文献信息

  • Hepatitis C Virus Inhibitors
    申请人:Bristol-Myers Squibb Company
    公开号:US20130183269A1
    公开(公告)日:2013-07-18
    The present disclosure is generally directed to antiviral compounds, and more specifically directed to combinations of compounds which can inhibit the function of the NS5A protein encoded by Hepatitis C virus (HCV), compositions comprising such combinations, and methods for inhibiting the function of the NS5A protein.
    本公开涉及抗病毒化合物,更具体地涉及能够抑制丙型肝炎病毒(HCV)编码的NS5A蛋白功能的化合物组合,包括这种组合的组成物,以及抑制NS5A蛋白功能的方法。
  • ANTIBACTERIAL AMINOGLYCOSIDE ANALOGS
    申请人:Aggen James Bradley
    公开号:US20110275586A1
    公开(公告)日:2011-11-10
    Compounds having antibacterial activity are disclosed. The compounds have the following structure (I): including stereoisomers, pharmaceutically acceptable salts and prodrugs thereof, wherein Q 1 , Q 2 , Z 1 , Z 2 , Z 3 , Z 4 , R 1 , R 2 and R 3 are as defined herein. Methods associated with preparation and use of such compounds, as well as pharmaceutical compositions comprising such compounds, are also disclosed.
    本文披露了具有抗菌活性的化合物。该化合物具有以下结构(I):包括立体异构体、药学上可接受的盐和前药,其中Q1、Q2、Z1、Z2、Z3、Z4、R1、R2和R3的定义如本文所述。本文还披露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制药组合物。
  • AMINOGLYCOSIDE DOSING REGIMENS
    申请人:Bruss Jon B.
    公开号:US20120208781A1
    公开(公告)日:2012-08-16
    The present invention provides new aminoglycoside dosing regimens associated with enhanced microbicidal activity and reduced nephrotoxicity, as well as methods of using these dosing regimens to treat various bacterial infections.
    本发明提供了新的氨基糖苷类药物给药方案,与增强微生物杀灭活性和降低肾毒性有关,并提供了使用这些给药方案治疗各种细菌感染的方法。
  • HEPATITIS C VIRUS INHIBITORS
    申请人:BRISTOL-MAYERS SQUIBB COMPANY
    公开号:US20160199355A1
    公开(公告)日:2016-07-14
    The present disclosure is generally directed to antiviral compounds, and more specifically directed to combinations of compounds which can inhibit the function of the NS5A protein encoded by Hepatitis C virus (HCV), compositions comprising such combinations, and methods for inhibiting the function of the NS5A protein.
    本公开涉及抗病毒化合物,更具体地涉及能够抑制丙型肝炎病毒(HCV)编码的NS5A蛋白功能的化合物组合、包含这种组合的组合物,以及抑制NS5A蛋白功能的方法。
  • Combinations of Hepatitis C Virus Inhibitors
    申请人:BRISTOL-MYERS SQUIBB COMPANY
    公开号:US20160158200A1
    公开(公告)日:2016-06-09
    The present disclosure is generally directed to antiviral compounds, and more specifically directed to combinations of compounds which can inhibit the function of the NS5A protein encoded by Hepatitis C virus (HCV), compositions comprising such combinations, and methods for inhibiting the function of the NS5A protein.
    本公开涉及抗病毒化合物,更具体地涉及能够抑制丙型肝炎病毒(HCV)编码的NS5A蛋白功能的化合物组合,包含这种组合的组合物,以及抑制NS5A蛋白功能的方法。
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