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4-[2-(3-Chlorophenyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyridin-3-yl]quinoline

中文名称
——
中文别名
——
英文名称
4-[2-(3-Chlorophenyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyridin-3-yl]quinoline
英文别名
——
4-[2-(3-Chlorophenyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyridin-3-yl]quinoline化学式
CAS
——
化学式
C22H18ClN3
mdl
——
分子量
359.8
InChiKey
SNQKFIWBMLNIBY-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):
    5.1
  • 重原子数:
    26
  • 可旋转键数:
    2
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    30.7
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • Novel pyrrole derivatives as pharmaceutical agents
    申请人:——
    公开号:US20040106604A1
    公开(公告)日:2004-06-03
    Novel pyrrazole derivative compounds and their use as pharmaceutical agents, in particular their use as TGF-beta signal transduction inhibitors. The disclosed invention relates to compounds of the structure (I) wherein (I) is a four, five, or six membered saturated ring and X is C, O or S. 1
    小说吡唑生物化合物及其作为药物代理的使用,特别是其作为TGF-beta信号转导抑制剂的使用。所公开的发明涉及结构(I)的化合物,其中(I)是四、五或六个成员的饱和环,X是C、O或S。1
  • EFFICIENT INDUCTION OF PLURIPOTENT STEM CELLS USING SMALL MOLECULE COMPOUNDS
    申请人:Ichida Justin
    公开号:US20120021519A1
    公开(公告)日:2012-01-26
    The disclosure features a method of producing a reprogrammed cell (e.g. an induced pluripotent stem cell or an undifferentiated cell) from a differentiated (e.g. somatic) cell. In some embodiments, the methods includes contacting a differentiated (e.g. somatic cell) with a TGFBR1 inhibitor or anti-TGF-β-antibody to produce a reprogrammed cell (e.g. pluripotent stem cell or undifferentiated cell). Embodiments of the present invention relate to a reprogrammed cell and methods and compositions for producing a chemically produced reprogrammed cell or populations thereof.
  • TGF-BETA RECEPTOR INHIBITORS TO ENHANCE DIRECT REPROGRAMMING
    申请人:THE GENERAL HOSPITAL CORPORATION
    公开号:US20140120621A1
    公开(公告)日:2014-05-01
    In general, iPS cells are produced by delivery of stem cell-associated genes into adult somatic cells (e.g., fibroblasts). Described herein are methods for enhancing the efficiency and rate of induced pluripotent stem cell production by treating somatic cells with a transforming growth factor-beta receptor (TGFβR) inhibitor. Also described herein are iPS cell compositions made according to the methods described herein and iPS cell compositions comprising an iPS cell in an admixture with a TGFβR inhibitor. Further described herein are kits for producing iPS cells using a TGFβR inhibitor.
  • COMPOSITIONS AND METHODS FOR IMPROVING INDUCED NEURON GENERATION
    申请人:PRESIDENT AND FELLOWS OF HARVARD COLLEGE
    公开号:US20160115447A1
    公开(公告)日:2016-04-28
    The present inventions relate to methods and compositions useful for improving the efficiency of inducing the generation of neurons from non-neuronal cell types, for example, by contacting the cell or cell culture medium with one or more agents which inhibit Activin and/or PLK1 signaling. Also disclosed are methods for promoting neuron survival, for example, by inhibiting Activin and/or PLK1 signaling, and methods for promoting the survival of intermediates in a cell differentiation pathway, for example, by inhibiting Activin and/or PLK1 signaling.
  • US7087626B2
    申请人:——
    公开号:US7087626B2
    公开(公告)日:2006-08-08
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