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(E)-<2-<2-<(2-amino-1,6-dihydro-6-oxo-9H-purin-9-yl)methyl>phenyl>-1-fluoroethenyl>phosphonic acid | 149365-37-7

中文名称
——
中文别名
——
英文名称
(E)-<2-<2-<(2-amino-1,6-dihydro-6-oxo-9H-purin-9-yl)methyl>phenyl>-1-fluoroethenyl>phosphonic acid
英文别名
[(E)-2-[2-[(2-amino-6-oxo-1H-purin-9-yl)methyl]phenyl]-1-fluoroethenyl]phosphonic acid
(E)-<2-<2-<(2-amino-1,6-dihydro-6-oxo-9H-purin-9-yl)methyl>phenyl>-1-fluoroethenyl>phosphonic acid化学式
CAS
149365-37-7
化学式
C14H13FN5O4P
mdl
——
分子量
365.26
InChiKey
AEMSKSDTIXCPHB-BJMVGYQFSA-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):
    -0.4
  • 重原子数:
    25
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    143
  • 氢给体数:
    4
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    (E)-<2-<2-<(2-amino-1,6-dihydro-6-chloro-9H-purin-9-yl)methyl>phenyl>-1-fluoroethenyl>phosphonic acid diethyl ester 在 盐酸三甲基溴硅烷 作用下, 生成 (E)-<2-<2-<(2-amino-1,6-dihydro-6-oxo-9H-purin-9-yl)methyl>phenyl>-1-fluoroethenyl>phosphonic acid
    参考文献:
    名称:
    Fluorophosphonate derivatives of N9-benzylguanine as potent, slow-binding multisubstrate analogue inhibitors of purine nucleoside phosphorylase
    摘要:
    The phosphonate derivatives of N-9-benzylguanine (4a-4h) have ban prepared as purine nucleoside phophorylase inhibitors. Enzyme inhibition studies with PNP from calf spleen or human erythrocyte show that compounds 4b and 4c are among the best PNP inhibitors ever reported, demonstrating further the importance of fluorines in such type of inhibitors.
    DOI:
    10.1016/0040-4020(95)00891-b
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文献信息

  • 9-Purinyl phosphonic acid derivatives
    申请人:MERRELL DOW PHARMACEUTICALS INC.
    公开号:EP0465297B1
    公开(公告)日:1996-01-31
  • US5494912A
    申请人:——
    公开号:US5494912A
    公开(公告)日:1996-02-27
  • US5538978A
    申请人:——
    公开号:US5538978A
    公开(公告)日:1996-07-23
  • US5527803A
    申请人:——
    公开号:US5527803A
    公开(公告)日:1996-06-18
  • Fluorophosphonate derivatives of N9-benzylguanine as potent, slow-binding multisubstrate analogue inhibitors of purine nucleoside phosphorylase
    作者:S. Halazy、A. Ehrhard、A. Eggenspiller、V. Berges-Gross、C. Danzin
    DOI:10.1016/0040-4020(95)00891-b
    日期:1996.1
    The phosphonate derivatives of N-9-benzylguanine (4a-4h) have ban prepared as purine nucleoside phophorylase inhibitors. Enzyme inhibition studies with PNP from calf spleen or human erythrocyte show that compounds 4b and 4c are among the best PNP inhibitors ever reported, demonstrating further the importance of fluorines in such type of inhibitors.
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