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1-(3-硝基苯磺酰基)氮丙啶 | 99055-45-5

中文名称
1-(3-硝基苯磺酰基)氮丙啶
中文别名
——
英文名称
1-<3-Nitro-benzolsulfonyl>-aziridin
英文别名
N-<3-Nitro-benzolsulfonyl>-aziridin;1-(3-nitro-benzenesulfonyl)-aziridine;1-((3-Nitrophenyl)sulfonyl)aziridine;1-(3-nitrophenyl)sulfonylaziridine
1-(3-硝基苯磺酰基)氮丙啶化学式
CAS
99055-45-5
化学式
C8H8N2O4S
mdl
——
分子量
228.229
InChiKey
VCUCDKQRUFADOG-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):
    0.2
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    91.4
  • 氢给体数:
    0
  • 氢受体数:
    5

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

  • 作为反应物:
    描述:
    1-(3-硝基苯磺酰基)氮丙啶 在 sodium carbonate 、 三氟乙酸 作用下, 以 二氯甲烷乙腈 为溶剂, 反应 8.0h, 生成 1-[2-(3-aminophenylsulfonylamino)ethyl]-4,7,10-tris(carboxymethyl)-1,4,7,10-tetraazacyclododecane
    参考文献:
    名称:
    Development of hypoxia-sensitive Gd3+-based MRI contrast agents
    摘要:
    Hypoxia occurs in various diseases, including cancer, ischemia, and acute and chronic vascular diseases. Here we describe the design and synthesis of the first hypoxia-sensitive MRI contrast agents, SAGds. SAGds showed a pH-dependent r(1) relaxivity change associated with intramolecular chelation of the nitrogen atom of the sulfonamide moiety to the Gd3+ center. There was a correlation between the pK(a) of the r(1) relaxivity change and the sum of the Hammett sigma constants of substituents on the aromatic ring. Among the synthesized compounds, 4NO(2)2MeOSAGd was selectively reduced to the amine by rat liver microsomes under hypoxic conditions, resulting in a 1.8-fold increment of the r(1) relaxivity owing to the change in pK(a) of the arylsulfonamide moiety. This enhancement of the r(1) relaxivity could be clearly detected in T-1-weighted MR images. Thus, 4NO(2)2MeOSAGd is a 'smart' MRI contrast agent for the detection of hypoxia under physiological conditions. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2012.02.071
  • 作为产物:
    描述:
    N-(2-羟基乙基)-3-硝基苯磺酰胺三乙胺 、 potassium hydroxide 作用下, 以 二氯甲烷甲苯 为溶剂, 反应 0.5h, 生成 1-(3-硝基苯磺酰基)氮丙啶
    参考文献:
    名称:
    Development of hypoxia-sensitive Gd3+-based MRI contrast agents
    摘要:
    Hypoxia occurs in various diseases, including cancer, ischemia, and acute and chronic vascular diseases. Here we describe the design and synthesis of the first hypoxia-sensitive MRI contrast agents, SAGds. SAGds showed a pH-dependent r(1) relaxivity change associated with intramolecular chelation of the nitrogen atom of the sulfonamide moiety to the Gd3+ center. There was a correlation between the pK(a) of the r(1) relaxivity change and the sum of the Hammett sigma constants of substituents on the aromatic ring. Among the synthesized compounds, 4NO(2)2MeOSAGd was selectively reduced to the amine by rat liver microsomes under hypoxic conditions, resulting in a 1.8-fold increment of the r(1) relaxivity owing to the change in pK(a) of the arylsulfonamide moiety. This enhancement of the r(1) relaxivity could be clearly detected in T-1-weighted MR images. Thus, 4NO(2)2MeOSAGd is a 'smart' MRI contrast agent for the detection of hypoxia under physiological conditions. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2012.02.071
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文献信息

  • Development of hypoxia-sensitive Gd3+-based MRI contrast agents
    作者:Shimpei Iwaki、Kenjiro Hanaoka、Wen Piao、Toru Komatsu、Tasuku Ueno、Takuya Terai、Tetsuo Nagano
    DOI:10.1016/j.bmcl.2012.02.071
    日期:2012.4
    Hypoxia occurs in various diseases, including cancer, ischemia, and acute and chronic vascular diseases. Here we describe the design and synthesis of the first hypoxia-sensitive MRI contrast agents, SAGds. SAGds showed a pH-dependent r(1) relaxivity change associated with intramolecular chelation of the nitrogen atom of the sulfonamide moiety to the Gd3+ center. There was a correlation between the pK(a) of the r(1) relaxivity change and the sum of the Hammett sigma constants of substituents on the aromatic ring. Among the synthesized compounds, 4NO(2)2MeOSAGd was selectively reduced to the amine by rat liver microsomes under hypoxic conditions, resulting in a 1.8-fold increment of the r(1) relaxivity owing to the change in pK(a) of the arylsulfonamide moiety. This enhancement of the r(1) relaxivity could be clearly detected in T-1-weighted MR images. Thus, 4NO(2)2MeOSAGd is a 'smart' MRI contrast agent for the detection of hypoxia under physiological conditions. (C) 2012 Elsevier Ltd. All rights reserved.
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