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Pyrazole and thiophene derivative 1

中文名称
——
中文别名
——
英文名称
Pyrazole and thiophene derivative 1
英文别名
6-(2-oxopiperidin-1-yl)-1-phenylpyrazolo[4,3-e][1,3]oxazin-4-one
Pyrazole and thiophene derivative 1化学式
CAS
——
化学式
C16H14N4O3
mdl
——
分子量
310.31
InChiKey
GHCGOVANSHYUTA-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):
    1.8
  • 重原子数:
    23
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    76.8
  • 氢给体数:
    0
  • 氢受体数:
    4

文献信息

  • Novel Heterocyclic Compound Classes for Signaling Modulation
    申请人:SignalRx Pharmaceuticals, Inc.
    公开号:US20150315207A1
    公开(公告)日:2015-11-05
    The invention relates to compounds of Formulas I-VII (or pharmaceutically acceptable salts thereof) as defined herein, pharmaceutical compositions thereof, and their use in manufactures and methods for modulating cellular signaling pathways and biological processes associated therewith including inhibition of kinase activity such as PI-3 kinase or inhibition of bromodomain proteins or both at the same time as well as to therapeutic methods for treating a disease associated with aberrant PI3K and/or bromodomain proteins.
    本发明涉及公式I-VII化合物(或其药学上可接受的盐),药物组合物以及它们在制造和调节细胞信号通路和与之相关的生物过程方面的用途,包括抑制激酶活性,如PI-3激酶或抑制域蛋白或同时抑制两者,以及治疗与异常PI3K和/或域蛋白相关的疾病的治疗方法。
  • Heterocyclic compound classes for signaling modulation
    申请人:SignalRx Pharmaceuticals, Inc.
    公开号:US10174032B2
    公开(公告)日:2019-01-08
    The invention relates to compounds of Formulas I-VII (or pharmaceutically acceptable salts thereof) as defined herein, pharmaceutical compositions thereof, and their use in manufactures and methods for modulating cellular signaling pathways and biological processes associated therewith including inhibition of kinase activity such as PI-3 kinase or inhibition of bromodomain proteins or both at the same time as well as to therapeutic methods for treating a disease associated with aberrant PI3K and/or bromodomain proteins.
    本发明涉及本文定义的式 I-VII 的化合物(或其药学上可接受的盐)、其药物组合物及其在制造和方法中的用途,用于调节细胞信号通路和与之相关的生物过程,包括抑制激酶活性(如 PI-3 激酶)或抑制链蛋白或同时抑制二者,以及用于治疗与异常 PI3K 和/或链蛋白相关疾病的治疗方法。
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