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1-(4-ethylphenyl)-6,7-dihydro-5H-pyrrolo[2,3-c]azepine-4,8-dione | 1323444-35-4

中文名称
——
中文别名
——
英文名称
1-(4-ethylphenyl)-6,7-dihydro-5H-pyrrolo[2,3-c]azepine-4,8-dione
英文别名
——
1-(4-ethylphenyl)-6,7-dihydro-5H-pyrrolo[2,3-c]azepine-4,8-dione化学式
CAS
1323444-35-4
化学式
C16H16N2O2
mdl
——
分子量
268.315
InChiKey
QIRIMPJZXKXFAO-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):
    2.2
  • 重原子数:
    20
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    51.1
  • 氢给体数:
    1
  • 氢受体数:
    2

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:
    2-(三氯乙酰)吡咯吡啶四磷十氧化物 、 copper(II) acetate monohydrate 、 三乙胺 、 sodium hydroxide 作用下, 以 二氯甲烷乙腈 为溶剂, 生成 1-(4-ethylphenyl)-6,7-dihydro-5H-pyrrolo[2,3-c]azepine-4,8-dione
    参考文献:
    名称:
    Pyrrolo[2,3-c]azepine derivatives: A new class of potent protein tyrosine phosphatase 1B inhibitors
    摘要:
    A series of pyrrolo[2,3-c] azepine derivatives was designed, synthesized, and evaluated as a new class of inhibitors against protein tyrosine phosphatase 1B (PTP1B) in vitro. The results demonstrated that compounds bearing a biphenyl moiety were proved to markedly influence the potency of these inhibitors. Particularly, compounds 29, 35 and 36 showed interesting inhibition with IC50 value of 16.36, 14.93 and 13.92 mu M, respectively. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2011.05.052
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文献信息

  • Pyrrolo[2,3-c]azepine derivatives: A new class of potent protein tyrosine phosphatase 1B inhibitors
    作者:Jianwei Xie、Jinying Tian、Li Su、Manna Huang、Xinhai Zhu、Fei Ye、Yiqian Wan
    DOI:10.1016/j.bmcl.2011.05.052
    日期:2011.7
    A series of pyrrolo[2,3-c] azepine derivatives was designed, synthesized, and evaluated as a new class of inhibitors against protein tyrosine phosphatase 1B (PTP1B) in vitro. The results demonstrated that compounds bearing a biphenyl moiety were proved to markedly influence the potency of these inhibitors. Particularly, compounds 29, 35 and 36 showed interesting inhibition with IC50 value of 16.36, 14.93 and 13.92 mu M, respectively. (C) 2011 Elsevier Ltd. All rights reserved.
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