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3-Hydroxy-1-imidazol-1-yl-4-methyl-3-[2-thiophen-3-yl-ethyl)-pentan-1-one | 261710-73-0

中文名称
——
中文别名
——
英文名称
3-Hydroxy-1-imidazol-1-yl-4-methyl-3-[2-thiophen-3-yl-ethyl)-pentan-1-one
英文别名
3-Hydroxy-1-imidazol-1-yl-4-methyl-3-(2-thiophen-3-ylethyl)pentan-1-one
3-Hydroxy-1-imidazol-1-yl-4-methyl-3-[2-thiophen-3-yl-ethyl)-pentan-1-one化学式
CAS
261710-73-0
化学式
C15H20N2O2S
mdl
——
分子量
292.402
InChiKey
WBKNXWOTMLKBCX-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):
    2.4
  • 重原子数:
    20
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.47
  • 拓扑面积:
    83.4
  • 氢给体数:
    1
  • 氢受体数:
    4

文献信息

  • HIV protease inhibitors
    申请人:——
    公开号:US20040106606A1
    公开(公告)日:2004-06-03
    The present invention relates to novel dihydropyrones with tethered heterocycles having improved pharmacologic properties which potently inhibit the HIV aspartyl protease blocking HIV infectivity. The dihydropyrones are useful in the development of therapies for the treatment of viral infections and diseases including AIDS. The present invention is also directed to methods of synthesis of the dihydropyrones and intermediates useful in the preparation of the final compounds.
    本发明涉及一种新颖的具有改进药理学性质的带有连接杂环的二喃并具有强烈抑制HIV天冬氨酸蛋白酶以阻止HIV感染性的药物。这些二喃可用于开发治疗病毒感染和疾病,包括艾滋病的治疗方案。本发明还涉及二喃的合成方法以及用于制备最终化合物的中间体
  • HIV PROTEASE INHIBITORS
    申请人:WARNER-LAMBERT COMPANY
    公开号:EP1112269A2
    公开(公告)日:2001-07-04
  • US6528510B1
    申请人:——
    公开号:US6528510B1
    公开(公告)日:2003-03-04
  • [EN] HIV PROTEASE INHIBITORS<br/>[FR] INHIBITEURS DE LA PROTEASE DU VIH
    申请人:WARNER LAMBERT CO
    公开号:WO2000015634A2
    公开(公告)日:2000-03-23
    The present invention relates to novel dihydropyrones with tethered heterocycles having improved pharmacologic properties which potently inhibit the HIV aspartyl protease blocking HIV infectivity. The dihydropyrones are useful in the development of therapies for the treatment of viral infections and diseases, including AIDS. The present invention is also directed to methods of synthesis of the dihydropyrones and intermediates useful in the preparation of the final compounds.
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