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1-(Oct-1-ylaminocarbonylmethyl)-2-(4-fluorobenzyl)thio-5-(pyrimid-5-ylmethyl)pyrimidin-4-one

中文名称
——
中文别名
——
英文名称
1-(Oct-1-ylaminocarbonylmethyl)-2-(4-fluorobenzyl)thio-5-(pyrimid-5-ylmethyl)pyrimidin-4-one
英文别名
2-[2-(4-Fluoro-benzylsulfanyl)-4-oxo-5-pyrimidin-5-ylmethyl-4H-pyrimidin-1-yl]-N-octyl-acetamide;2-[2-[(4-fluorophenyl)methylsulfanyl]-4-oxo-5-(pyrimidin-5-ylmethyl)pyrimidin-1-yl]-N-octylacetamide
1-(Oct-1-ylaminocarbonylmethyl)-2-(4-fluorobenzyl)thio-5-(pyrimid-5-ylmethyl)pyrimidin-4-one化学式
CAS
——
化学式
C26H32FN5O2S
mdl
——
分子量
497.637
InChiKey
BBBNQDNNKDVNPO-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):
    5
  • 重原子数:
    35
  • 可旋转键数:
    14
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    113
  • 氢给体数:
    1
  • 氢受体数:
    6

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

  • 作为产物:
    描述:
    (Z)-3-Methoxy-2-pyrimidin-5-ylmethyl-acryloyl chloride 在 N,N-二异丙基乙胺 作用下, 以 二氯甲烷N,N-二甲基甲酰胺乙腈 为溶剂, 生成 1-(Oct-1-ylaminocarbonylmethyl)-2-(4-fluorobenzyl)thio-5-(pyrimid-5-ylmethyl)pyrimidin-4-one
    参考文献:
    名称:
    The identification of a potent, water soluble inhibitor of lipoprotein-associated phospholipase A2
    摘要:
    Modification of the pyrimidone 5-substituent in a series of 1-((amidolinked)-alkyl)-pyrimidones, lipophilic inhibitors of lipoprotein-associated phospholipase A(2), has given inhibitors of nanomolar potency and improved physicochemical properties. Compound 23 was identified as a potent, highly water soluble, CNS penetrant inhibitor suitable for intravenous administration. (C) 2001 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(01)00038-5
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文献信息

  • [EN] PYRIMIDINONE COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM<br/>[FR] COMPOSES DE PYRIMIDINONE ET COMPOSITIONS PHARMACEUTIQUES LES RENFERMANT
    申请人:SMITHKLINE BEECHAM PLC
    公开号:WO1999024420A1
    公开(公告)日:1999-05-20
    (EN) A group of novel pyrimidone compounds are inhibitors of the enzyme LDL PLA2 and therefore of use in treating atherosclerosis.(FR) L'invention concerne un groupe de nouveaux composés de pyrimidinone qui sont des inhibiteurs de l'enzyme LDL PLA2 et qui s'utilisent donc pour le traitement de l'athérosclérose.
    一组新型嘧啶酮化合物是LDL PLA2酶的抑制剂,因此可用于治疗动脉粥样硬化。
  • Pyrimidinone compounds and pharmaceutical compositions containing them
    申请人:——
    公开号:US20020120139A1
    公开(公告)日:2002-08-29
    A group of novel pyrimidone compounds are inhibitors of the enzyme LDL PLA2 and therefore of use in treating atherosclerosis.
    一组新型嘧啶酮化合物是LDL PLA2酶的抑制剂,因此可用于治疗动脉粥样硬化。
  • N-1 substituted pyrimidin-4-ones: novel, orally active inhibitors of lipoprotein-associated phospholipase A2
    作者:Helen F. Boyd、Stephen C.M. Fell、Sean T. Flynn、Deirdre M.B. Hickey、Robert J. Ife、Colin A. Leach、Colin H. Macphee、Kevin J. Milliner、Kitty E. Moores、Ivan L. Pinto、Rod A. Porter、D.Anthony Rawlings、Stephen A. Smith、Ian G. Stansfield、David G. Tew、Colin J. Theobald、Caroline M. Whittaker
    DOI:10.1016/s0960-894x(00)00510-2
    日期:2000.11
    From two related series of 2-(alkylthio)-pyrimidones, a novel series of 1-((amidolinked)-alkyl)-pyrimidones has been designed as nanomolar inhibitors of human lipoprotein-associated phopholipase A(2). These compounds show greatly enhanced activity in isolated plasma. Selected derivatives such as compounds 51 and 52 are orally active with a good duration of action. (C) 2000 Elsevier Science Ltd. All rights reserved.
  • PYRIMIDINONE COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
    申请人:SmithKline Beecham plc
    公开号:EP1028955B1
    公开(公告)日:2003-07-16
  • US6417192B1
    申请人:——
    公开号:US6417192B1
    公开(公告)日:2002-07-09
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