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N-(4-fluorobenzyl)-5,6-dihydroxy-2-(pyridin-2-yl)pyrimidine-4-carboxamide

中文名称
——
中文别名
——
英文名称
N-(4-fluorobenzyl)-5,6-dihydroxy-2-(pyridin-2-yl)pyrimidine-4-carboxamide
英文别名
N-[(4-fluorophenyl)methyl]-5,6-dihydroxy-2-(2-pyridyl)pyrimidine-4-carboxamide;N-[(4-fluorophenyl)methyl]-5-hydroxy-6-oxo-2-pyridin-2-yl-1H-pyrimidine-4-carboxamide
N-(4-fluorobenzyl)-5,6-dihydroxy-2-(pyridin-2-yl)pyrimidine-4-carboxamide化学式
CAS
——
化学式
C17H13FN4O3
mdl
——
分子量
340.314
InChiKey
WRKSGPVYRPHZKM-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):
    1.7
  • 重原子数:
    25
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    104
  • 氢给体数:
    3
  • 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:
    dimethyl 2-((picolinimidamido)oxy)but-2-enedioate 以 N,N-二甲基甲酰胺 、 xylene 为溶剂, 反应 3.0h, 生成 N-(4-fluorobenzyl)-5,6-dihydroxy-2-(pyridin-2-yl)pyrimidine-4-carboxamide
    参考文献:
    名称:
    Dihydroxypyrimidine-4-carboxamides作为新型有效和选择性的HIV整合酶抑制剂。
    摘要:
    人类免疫缺陷病毒1型(HIV-1)整合酶是复制所需的三种组成型病毒酶之一,是化学疗法干预AIDS的合理靶标,最近在临床环境中也得到了证实。我们在这里报告的N-苄基5,6-二羟基嘧啶-4-羧酰胺的设计和合成作为一类药物,对HIV整合酶催化的链转移过程具有有效的抑制作用。在当前的研究中,对这些分子进行了结构修饰,以检查其对HIV整合酶抑制效能的影响。该系列中最有趣的化合物之一是2- [1-(二甲基氨基)-1-甲基乙基] -N-(4-氟苄基)-5,6-二羟基嘧啶-4-羧酰胺38,CIC95为78 nM。在血清蛋白存在下进行基于细胞的测定。
    DOI:
    10.1021/jm070027u
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文献信息

  • [EN] PYRIMIDINONE COMPOUNDS AND METHODS FOR PREVENTING AND TREATING INFLUENZA<br/>[FR] COMPOSÉS DE PYRIMIDINONE ET MÉTHODES DE PRÉVENTION ET DE TRAITEMENT DE LA GRIPPE
    申请人:ST JUDE CHILDRENS RES HOSPITAL
    公开号:WO2012151567A1
    公开(公告)日:2012-11-08
    In one aspect, the invention relates to novel, broad-spectrum anti-viral, pyrimidinone compounds, methods of use, compositions and kits useful in treating and/or preventing influenza. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.
    在一个方面,该发明涉及新颖的、广谱抗病毒的嘧啶酮化合物,以及用于治疗和/或预防流感的方法、组合物和工具包。本摘要旨在作为在特定领域进行搜索的扫描工具,并不意味着对本发明的限制。
  • Dihydroxypyrimidine carboxamide inhibitors of hiv integrase
    申请人:Di Francesco E. Maria
    公开号:US20050075356A1
    公开(公告)日:2005-04-07
    4,5-Dihydroxypyrimidine-6-carboxamides of formula (I); are described as inhibitors of HIV integrase and inhibitors of HIV replication, wherein R 1 , R 2 , R 3 and R 4 are defined herein. These compounds are useful in the prevention and treatment of infection by HIV and in the prevention, delay in the onset, and treatment of AIDS. The compounds are employed against HIV infection and AIDS as compounds per se or in the form of pharmaceutically acceptable salts. The compounds and their salts can be employed as ingredients in pharmaceutical compositions, optionally in combination with other antivirals, immunomodulators, antibiotics or vaccines. Methods of preventing, treating or delaying the onset of AIDS and methods of preventing or treating infection by HIV are also described.
    本文描述了式(I)的4,5-二羟基嘧啶-6-羧酰胺类化合物作为HIV整合酶抑制剂和HIV复制抑制剂,其中R1,R2,R3和R4在此定义。这些化合物在预防和治疗HIV感染以及预防,延迟发病和治疗艾滋病方面非常有用。这些化合物可作为化合物本身或作为药物可接受的盐的形式用于对抗HIV感染和艾滋病。这些化合物及其盐可作为药物组合物中的成分,可选择与其他抗病毒药物,免疫调节剂,抗生素或疫苗组合使用。还描述了预防,治疗或延迟艾滋病发病的方法以及预防或治疗HIV感染的方法。
  • Dihydroxypyrimidine carboxamide inhibitors of HIV integrase
    申请人:Di Francesco E. Maria
    公开号:US20070083045A1
    公开(公告)日:2007-04-12
    4,5-Dihydroxypyrimidine-6-carboxamides of formula: are described as inhibitors of HIV integrase and inhibitors of HIV replication, wherein R 1 , R 2 , R 3 and R 4 are defined herein. These compounds are useful in the prevention and treatment of infection by HIV and in the prevention, delay in the onset, and treatment of AIDS. The compounds are employed against HIV infection and AIDS as compounds per se or in the form of pharmaceutically acceptable salts. The compounds and their salts can be employed as ingredients in pharmaceutical compositions, optionally in combination with other antivirals, immunomodulators, antibiotics or vaccines. Methods of preventing, treating or delaying the onset of AIDS and methods of preventing or treating infection by HIV are also described.
    本文描述了式子中R1,R2,R3和R4被定义的4,5-二羟基嘧啶-6-羧酰胺化合物,其作为HIV整合酶抑制剂和HIV复制抑制剂。这些化合物对于预防和治疗HIV感染以及预防、延迟AIDS发病和治疗AIDS非常有用。这些化合物可以作为化合物本身或药物可接受的盐形式用于对抗HIV感染和AIDS。这些化合物及其盐可以与其他抗病毒药物、免疫调节剂、抗生素或疫苗组合使用,作为制药组合物的成分。本文还描述了预防、治疗或延迟AIDS发病以及预防或治疗HIV感染的方法。
  • DIHYDROXYPYRIMIDINE CARBOXAMIDE INHIBITORS OF HIV INTEGRASE
    申请人:Istituto di Richerche di Biologia Molecolare P. Angeletti S.p.A.
    公开号:EP1441734B1
    公开(公告)日:2007-02-28
  • PYRIMIDINONE COMPOUNDS AND METHODS FOR PREVENTING AND TREATING INFLUENZA
    申请人:Webb Thomas R.
    公开号:US20140079666A1
    公开(公告)日:2014-03-20
    In one aspect, the invention relates to novel, broad-spectrum anti-viral, pyrimidinone compounds, methods of use, compositions and kits useful in treating and/or preventing influenza. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.
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