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(2,6-Dichlorophenyl)-[2-(2,6-difluorophenoxy)-9-ethyl-9H-purin-8-yl]-amine

中文名称
——
中文别名
——
英文名称
(2,6-Dichlorophenyl)-[2-(2,6-difluorophenoxy)-9-ethyl-9H-purin-8-yl]-amine
英文别名
N-(2,6-dichlorophenyl)-2-(2,6-difluorophenoxy)-9-ethylpurin-8-amine
(2,6-Dichlorophenyl)-[2-(2,6-difluorophenoxy)-9-ethyl-9H-purin-8-yl]-amine化学式
CAS
——
化学式
C19H13Cl2F2N5O
mdl
——
分子量
436.248
InChiKey
ITNVIICTIUQADS-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):
    5.5
  • 重原子数:
    29
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    64.9
  • 氢给体数:
    1
  • 氢受体数:
    7

反应信息

  • 作为产物:
    描述:
    2,6-二氟苯酚 在 palladium on activated charcoal 氢气N,N-二异丙基乙胺三氯氧磷 作用下, 以 四氢呋喃乙醇二氯甲烷 为溶剂, 反应 33.0h, 生成 (2,6-Dichlorophenyl)-[2-(2,6-difluorophenoxy)-9-ethyl-9H-purin-8-yl]-amine
    参考文献:
    名称:
    The development of novel C-2, C-8, and N-9 trisubstituted purines as inhibitors of TNF-α production
    摘要:
    A series of C-2, C-8, and N-9 trisubstituted purine based inhibitors of TNF-alpha production are described. The most potent analogs showed low nanomolar activity against LPS-induced TNF-alpha production in a THP-1 cell based assay. The SAR of the series was optimized with the aid of X-ray co-crystal structures of these inhibitors bound with mutated p38 (mp38).
    DOI:
    10.1016/j.bmcl.2006.05.050
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文献信息

  • US7256196B1
    申请人:——
    公开号:US7256196B1
    公开(公告)日:2007-08-14
  • The development of novel C-2, C-8, and N-9 trisubstituted purines as inhibitors of TNF-α production
    作者:Mark Sabat、John C. VanRens、Michael P. Clark、Todd A. Brugel、Jennifer Maier、Roger G. Bookland、Matthew J. Laufersweiler、Steven K. Laughlin、Adam Golebiowski、Biswanath De、Lily C. Hsieh、Richard L. Walter、Marlene J. Mekel、Michael J. Janusz
    DOI:10.1016/j.bmcl.2006.05.050
    日期:2006.8
    A series of C-2, C-8, and N-9 trisubstituted purine based inhibitors of TNF-alpha production are described. The most potent analogs showed low nanomolar activity against LPS-induced TNF-alpha production in a THP-1 cell based assay. The SAR of the series was optimized with the aid of X-ray co-crystal structures of these inhibitors bound with mutated p38 (mp38).
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