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2-Hydroxy-3-[(2-methylpropan-2-yl)oxycarbonylamino]hex-5-enoic acid | 274918-47-7

中文名称
——
中文别名
——
英文名称
2-Hydroxy-3-[(2-methylpropan-2-yl)oxycarbonylamino]hex-5-enoic acid
英文别名
——
2-Hydroxy-3-[(2-methylpropan-2-yl)oxycarbonylamino]hex-5-enoic acid化学式
CAS
274918-47-7
化学式
C11H19NO5
mdl
——
分子量
245.276
InChiKey
YCVRIOLIDRSHAB-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
  • 重原子数:
    17
  • 可旋转键数:
    7
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.64
  • 拓扑面积:
    95.9
  • 氢给体数:
    3
  • 氢受体数:
    5

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    2-Hydroxy-3-[(2-methylpropan-2-yl)oxycarbonylamino]hex-5-enoic acid盐酸 、 (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate 、 N,N-二异丙基乙胺 作用下, 以 1,4-二氧六环N,N-二甲基甲酰胺 为溶剂, 生成 tert-butyl (4S)-5-[[(2S)-1-[[(2S)-1-[(2S)-2-[[2-hydroxy-1-oxo-1-(prop-2-enylamino)hex-5-en-3-yl]carbamoyl]pyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]amino]-4-[[(2S)-4-[(2-methylpropan-2-yl)oxy]-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-oxobutanoyl]amino]-5-oxopentanoate
    参考文献:
    名称:
    α-Ketoamides, α-ketoesters and α-diketones as HCV NS3 protease inhibitors
    摘要:
    Peptide-based alpha-ketoamides, alpha-ketoesters and alpha-diketones were designed, synthesized and evaluated against HCV NS3 protease. alpha-Ketoamides have the highest affinity among the three classes, with 8 being the most potent inhibitor with an IC50 Of 340 nM. (C) 2000 DuPont Pharmaceuticals Company. Published by Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(00)00074-3
  • 作为产物:
    描述:
    Nα-(tert-butoxycarbonyl)allylglycine-N-methoxy-N-methylamide 在 lithium aluminium tetrahydride 、 TEA 、 sodium carbonate 作用下, 以 四氢呋喃二氯甲烷 为溶剂, 生成 2-Hydroxy-3-[(2-methylpropan-2-yl)oxycarbonylamino]hex-5-enoic acid
    参考文献:
    名称:
    α-Ketoamides, α-ketoesters and α-diketones as HCV NS3 protease inhibitors
    摘要:
    Peptide-based alpha-ketoamides, alpha-ketoesters and alpha-diketones were designed, synthesized and evaluated against HCV NS3 protease. alpha-Ketoamides have the highest affinity among the three classes, with 8 being the most potent inhibitor with an IC50 Of 340 nM. (C) 2000 DuPont Pharmaceuticals Company. Published by Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(00)00074-3
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文献信息

  • ORGANIC COMPOUNDS AND THEIR USES
    申请人:Brandl Trixl
    公开号:US20100204159A1
    公开(公告)日:2010-08-12
    The present application describes organic compounds that are useful for the treatment, prevention and/or amelioration of human diseases.
    本申请描述了对人类疾病的治疗、预防和/或改善有用的有机化合物。
  • α-Ketoamides, α-ketoesters and α-diketones as HCV NS3 protease inhibitors
    作者:Wei Han、Zilun Hu、Xiangjun Jiang、Carl P. Decicco
    DOI:10.1016/s0960-894x(00)00074-3
    日期:2000.4
    Peptide-based alpha-ketoamides, alpha-ketoesters and alpha-diketones were designed, synthesized and evaluated against HCV NS3 protease. alpha-Ketoamides have the highest affinity among the three classes, with 8 being the most potent inhibitor with an IC50 Of 340 nM. (C) 2000 DuPont Pharmaceuticals Company. Published by Elsevier Science Ltd. All rights reserved.
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