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化合物HJC0197 | 1383539-73-8

中文名称
化合物HJC0197
中文别名
——
英文名称
4-cyclopentyl-2-(2,5-dimethylbenzylsulfanyl)-6-oxo-1,6-dihydropyrimidine-5-carbonitrile
英文别名
HJC0197;4-Cyclopentyl-2-((2,5-dimethylbenzyl)thio)-6-oxo-1,6-dihydropyrimidine-5-carbonitrile;4-cyclopentyl-2-[(2,5-dimethylphenyl)methylsulfanyl]-6-oxo-1H-pyrimidine-5-carbonitrile
化合物HJC0197化学式
CAS
1383539-73-8
化学式
C19H21N3OS
mdl
——
分子量
339.461
InChiKey
QLLWRTHDHRGHQZ-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):
    4
  • 重原子数:
    24
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    90.6
  • 氢给体数:
    1
  • 氢受体数:
    4

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:
    环戊基甲醛哌啶potassium carbonate 作用下, 以 乙醇丙酮 为溶剂, 反应 7.0h, 生成 化合物HJC0197
    参考文献:
    名称:
    [EN] MODULATORS OF EXCHANGE PROTEINS DIRECTLY ACTIVATED BY CAMP (EPACS)
    [FR] MODULATEURS DE PROTÉINES D'ÉCHANGE DIRECTEMENT ACTIVÉES PAR L'AMPC (EPAC)
    摘要:
    该发明的实施例涉及抑制EPAC蛋白活性的化合物以及使用这些化合物的方法。发明人已经开发了一种敏感且稳健的高通量筛选(HTS)测定方法,用于识别EPAC特异性抑制剂(Tsalkova等人(2012年)PLOS ONE 7(1):e30441)。
    公开号:
    WO2013119931A1
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文献信息

  • [EN] MODULATORS OF EXCHANGE PROTEINS DIRECTLY ACTIVATED BY CAMP (EPACS)<br/>[FR] MODULATEURS DE PROTÉINES D'ÉCHANGE DIRECTEMENT ACTIVÉES PAR L'AMPC (EPAC)
    申请人:UNIV TEXAS
    公开号:WO2013119931A1
    公开(公告)日:2013-08-15
    Embodiments of the invention are directed to compounds that inhibit an activity of EP AC proteins and methods of using the same. The inventors have developed a sensitive and robust high throughput screening (HTS) assay for the purpose of identifying EPAC specific inhibitors (Tsalkova et al. (2012) PLOS ONE 7(1 ):e30441).
    该发明的实施例涉及抑制EPAC蛋白活性的化合物以及使用这些化合物的方法。发明人已经开发了一种敏感且稳健的高通量筛选(HTS)测定方法,用于识别EPAC特异性抑制剂(Tsalkova等人(2012年)PLOS ONE 7(1):e30441)。
  • MODULATORS OF EXCHANGE PROTEINS DIRECTLY ACTIVATED BY CAMP (EPACS)
    申请人:The Board of Regents of the University of Texas System
    公开号:US20150110809A1
    公开(公告)日:2015-04-23
    Embodiments of the invention are directed to compounds that inhibit an activity of EP AC proteins and methods of using the same. The inventors have developed a sensitive and robust high throughput screening (HTS) assay for the purpose of identifying EPAC specific inhibitors (Tsalkova et al. (2012) PLOS ONE 7 (1):e30441).
    本发明的实施例涉及抑制EPAC蛋白活性的化合物及其使用方法。发明人开发了一种灵敏且强大的高通量筛选(HTS)检测方法,以识别EPAC特异性抑制剂(Tsalkova等人(2012)PLOS ONE 7(1):e30441)。
  • METHODS OF TREATING RICKETTSIA USING EXCHANGE PROTEINS DIRECTLY ACTIVATED BY CAMP (EPACS) INHIBITORS
    申请人:Gong Bin
    公开号:US20140348853A1
    公开(公告)日:2014-11-27
    Embodiments of the invention are directed to compounds that inhibit an activity of EPAC proteins and methods of using the same.
  • METHODS OF MODULATING MELANOSOME PH AND MELANIN LEVEL IN CELLS
    申请人:Cornell University
    公开号:US20190256856A1
    公开(公告)日:2019-08-22
    The invention is directed to compositions and methods for increasing the pH of a melanosome in a melanocyte, darkening skin or hair pigmentation, or treating a disease associated with decreased melanin comprising administering a soluble adenylyl cyclase (sAC) inhibitor and/or an exchange protein activated by cyclic AMP (EPAC) inhibitor to the melanocyte. The invention also provides compositions and methods for decreasing the pH of a melanosome in a melanocyte, lightening skin or hair pigmentation, or treating a disease associated with increased melanin comprising administering a sAC activator and/or an EPAC activator to the melanocyte.
  • METHODS AND COMPOSITIONS FOR GENERATING HEMATOPOIETIC CELLS
    申请人:Longboat Amniotics
    公开号:US20200048609A1
    公开(公告)日:2020-02-13
    Maturation signals provided via cyclic adenosine monophosphate (cAMP)/ E xchange p roteins a ctivated by c AMP (Epac) signaling during in vitro generation of blood cells from reprogrammed cells or pluripotent stem cells achieve superior function of hematopoietic cells differentiated from stem cells. The cAMP/Epac signaling enables an increased efficiency of production of precursor to blood and to blood cells. These generated blood cells can be utilized for therapeutics, treatments, disease prevention, drug discovery, personalized medicine, regenerative medicine, cell and tissue generation, universal donor banks and related methods and compositions.
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