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2,5-dinitro-2,5-bis-(3-oxo-butyl)-adiponitrile | 100971-06-0

中文名称
——
中文别名
——
英文名称
2,5-dinitro-2,5-bis-(3-oxo-butyl)-adiponitrile
英文别名
——
2,5-dinitro-2,5-bis-(3-oxo-butyl)-adiponitrile化学式
CAS
100971-06-0
化学式
C14H18N4O6
mdl
——
分子量
338.32
InChiKey
UKHISVKBVOBTOM-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

反应信息

  • 作为产物:
    描述:
    丁烯酮 、 alkaline earth salt of/the/ methylsulfuric acid 在 盐酸甲醇 作用下, 生成 2,5-dinitro-2,5-bis-(3-oxo-butyl)-adiponitrile
    参考文献:
    名称:
    Quantification of Skeletal Kinetic Indices in Paget's Disease Using Dynamic18F-Fluoride Positron Emission Tomography
    摘要:
    The purpose of this study was to quantify indices of regional bone metabolism in Paget's disease and to compare these indices with normal bone using dynamic18F‐fluoride positron emission tomography (PET). Seven patients with vertebral Paget's disease had 1 h dynamic18F‐fluoride PET scans performed. The scans included a diseased vertebra and an adjacent normal vertebra. Arterial plasma input functions were also measured. A three‐compartment, four‐parameter model was used with nonlinear regression analysis to estimate bone kinetic variables. Compared with normal bone, pagetic bone demonstrated higher values of plasma clearance to bone mineral (Ki; 1.03 × 10−1 vs. 0.36 × 10−1 ml/min per milliliter; p = 0.018) and clearance to total bone tissue (K1; 2.38 × 10−1 vs. 1.25 × 10−1 ml/min per milliliter; p = 0.018), reflecting increased mineralization and blood flow, respectively. Release of18F‐fluoride from bone mineral (k4) was lower in pagetic bone (p = 0.022), suggesting tighter binding of18F‐fluoride to bone mineral. The notional volume of the extravascular bone compartment (K1/k2) was greater in pagetic bone (p = 0.018). Although the unidirectional extraction efficiency from the extravascular space to bone mineral (Ki/K1) was greater in pagetic bone (p = 0.018), a lower pagetic value of k2 (p = 0.028), describing the rate of transfer from the bone extravascular compartment to plasma, suggests that the18F‐fluoride that enters the relatively fibrotic marrow space of pagetic bone may be less accessible for return to plasma. These findings confirm some of the known pathophysiology of Paget's disease, introduce some new observations, and show how dynamic18F‐fluoride PET may be of value in the measurement of regional metabolic parameters in focal bone disorders.
    DOI:
    10.1359/jbmr.2002.17.5.854
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