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ethyl 2-diazo-2-(7-hydroxy-2-oxaspiro[3.5]nonan-7-yl)acetate | 1557247-85-4

中文名称
——
中文别名
——
英文名称
ethyl 2-diazo-2-(7-hydroxy-2-oxaspiro[3.5]nonan-7-yl)acetate
英文别名
ethyl (2E)-2-diazo-2-(7-hydroxy-2-oxaspiro[3.5]nonan-7-yl)acetate
ethyl 2-diazo-2-(7-hydroxy-2-oxaspiro[3.5]nonan-7-yl)acetate化学式
CAS
1557247-85-4
化学式
C12H18N2O4
mdl
——
分子量
254.286
InChiKey
WFEYHSYBRHSJRY-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):
    1.4
  • 重原子数:
    18
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.83
  • 拓扑面积:
    57.8
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    ethyl 2-diazo-2-(7-hydroxy-2-oxaspiro[3.5]nonan-7-yl)acetate三乙胺三氟乙酸酐 作用下, 以 二氯甲烷 为溶剂, 反应 0.25h, 生成
    参考文献:
    名称:
    [EN] PYRAZOLE CARBOXAMIDE COMPOUNDS, COMPOSITIONS AND METHODS OF USE
    [FR] COMPOSÉS PYRAZOLE CARBOXAMIDES, COMPOSITIONS ET PROCÉDÉS D'UTILISATION
    摘要:
    本文提供了以下式(AA)的化合物:N N H HN O N N R R 6 A(R a)p,(AA)立体异构体或其药学上可接受的盐,其中A、R a、p、R和R 6在此处有定义,包括这些化合物的组合物以及用于治疗疾病的制备和使用这些化合物的方法。
    公开号:
    WO2014023258A1
  • 作为产物:
    参考文献:
    名称:
    Property- and Structure-Guided Discovery of a Tetrahydroindazole Series of Interleukin-2 Inducible T-Cell Kinase Inhibitors
    摘要:
    Interleukin-2 inducible T-cell kinase (ITK), a member of the Tec family of tyrosine kinases, plays a major role in T-cell signaling downstream of the T-cell receptor (TCR), and considerable efforts have been directed toward discovery of ITK-selective inhibitors as potential treatments of inflammatory disorders such as asthma. Using a previously disclosed indazole series of inhibitors as a starting point, and using X-ray crystallography and solubility forecast index (SFI) as guides, we evolved a series of tetrahydroindazole inhibitors with improved potency, selectivity, and pharmaceutical properties. Highlights include identification of a selectivity pocket above the ligand plane, and identification of appropriate lipophilic substituents to occupy this space. This effort culminated in identification of a potent and selective ITK inhibitor (GNE-9822) with good ADME properties in preclinical species.
    DOI:
    10.1021/jm500550e
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文献信息

  • PYRAZOLE CARBOXAMIDE COMPOUNDS, COMPOSITIONS AND METHODS OF USE
    申请人:Genentech, Inc.
    公开号:US20150158851A1
    公开(公告)日:2015-06-11
    Provided herein are compounds of formula (AA): stereoisomers or a pharmaceutically acceptable salt thereof, wherein A, R a , p, R 5 and R 6 are defined herein, compositions including the compounds and methods of manufacturing and using the compounds for the treatment of diseases.
    本文提供了式(AA)的化合物:其立体异构体或其药学上可接受的盐,其中A、Ra、p、R5和R6在此定义,包括该化合物的组合物以及制造和使用该化合物治疗疾病的方法。
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