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4-(3-Iodo-phenyl)-2,4-dioxo-butyric acid methyl ester | 956267-47-3

中文名称
——
中文别名
——
英文名称
4-(3-Iodo-phenyl)-2,4-dioxo-butyric acid methyl ester
英文别名
Methyl 4-(3-iodophenyl)-2,4-dioxobutanoate
4-(3-Iodo-phenyl)-2,4-dioxo-butyric acid methyl ester化学式
CAS
956267-47-3
化学式
C11H9IO4
mdl
——
分子量
332.095
InChiKey
IXWBIPAWSJATDB-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

物化性质

  • 沸点:
    420.0±30.0 °C(Predicted)
  • 密度:
    1.719±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.2
  • 重原子数:
    16
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    60.4
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    4-(3-Iodo-phenyl)-2,4-dioxo-butyric acid methyl ester盐酸羟胺 作用下, 以 甲醇 为溶剂, 反应 4.0h, 以72%的产率得到5-(3-iodo-phenyl)-isoxazole-3-carboxylic acid methyl ester
    参考文献:
    名称:
    MGluR5 modulators V
    摘要:
    本发明涉及新化合物,以及用于它们制备的方法,它们在治疗中的应用以及包含这些新化合物的药物组合物。
    公开号:
    US20070259860A1
  • 作为产物:
    描述:
    草酸二甲酯3-碘苯乙酮 在 sodium hydride 、 盐酸 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 2.0h, 以71.3%的产率得到4-(3-Iodo-phenyl)-2,4-dioxo-butyric acid methyl ester
    参考文献:
    名称:
    MGluR5 modulators V
    摘要:
    本发明涉及新化合物,以及用于它们制备的方法,它们在治疗中的应用以及包含这些新化合物的药物组合物。
    公开号:
    US20070259860A1
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文献信息

  • Substituted piperazines as metabotropic glutamate receptor antagonists
    申请人:Edwards Louise
    公开号:US20070037820A1
    公开(公告)日:2007-02-15
    The invention relates to compounds of formula I or pharmaceutically acceptable salts or solvates thereof: where Ar 1 , Ar 2 , Hy, L, R 1 , m and n are as defined in the description. The invention also includes pharmaceutical compositions and uses thereof, processes for making the compounds, as well as methods for the medical treatment of mGluR5-mediated disorders.
    这项发明涉及公式I的化合物或其药用可接受的盐或溶剂: 其中Ar1,Ar2,Hy,L,R1,m和n如描述中所定义。该发明还包括药物组合物及其用途,制备这些化合物的方法,以及治疗mGluR5介导的疾病的方法。
  • MGluR5 modulators VI
    申请人:Isaac Methvin
    公开号:US20070259895A1
    公开(公告)日:2007-11-08
    The present invention is directed to novel compounds, to a process for their preparation, their use in therapy and pharmaceutical compositions comprising the novel compounds.
    本发明涉及新化合物,以及用于它们制备的方法,它们在治疗中的应用以及包含这些新化合物的药物组合物。
  • [<sup>123</sup>I]-Celecoxib Analogues as SPECT Tracers of Cyclooxygenase-2 in Inflammation
    作者:Md. Jashim Uddin、Brenda C. Crews、Kebreab Ghebreselasie、Mohammed N. Tantawy、Lawrence J. Marnett
    DOI:10.1021/ml100232q
    日期:2011.2.10
    We report the synthesis and evaluation of a series of iodinated celecoxib analogues as cyclooxygenase-2 (COX-2)-targeted single photon emission computerized tomography (SPECT)-imaging agents for the detection of inflammation. The structure-activity relationship identified 5-(4-iodophenyl)-1-4-(methylsulfonyl)-phenyl}-3-(trifuloromethyl)-1H-pyrazole (8) as a promising compound with IC50 values of 0.05 mu M against purified COX-2 and 0.03 mu M against COX-2 in activated macrophages. The arylstannane of 8-undergoes facile radio-[I-123]-iodination upon treatment with (NaI)-I-123/NaI and chloramine T using an EtOAc/H2O two-phase system. The [I-123]-8 was produced in a radiochemical yield of 85% and a radiochemical purity of 99%. In vivo SPECT imaging demonstrated that the radiotracer was taken up by inflamed rat paws with an average 1.7-fold enrichment over contralateral noninflamed paws. This study suggests that conversion of celecoxib into its isomeric iodo [I-123]-analogues is a useful approach for generating novel and efficacious agents for COX-2-targeted SPECT imaging of inflammation.
  • [EN] MGLUR5 MODULATORS VI<br/>[FR] MODULATEURS DES RÉCEPTEURS MGLUR5 VI
    申请人:ASTRAZENECA AB
    公开号:WO2007130825A2
    公开(公告)日:2007-11-15
    [EN] The present invention is directed to novel compounds, to a process for their preparation, their use in therapy and pharmaceutical compositions comprising the novel compounds.
    [FR] la présente invention concerne des nouveaux composés, un processus de préparation de ceux-ci, leur utilisation thérapeutique et des compositions pharmaceutiques comprenant ces nouveaux composés.
  • [EN] MGLUR5 MODULATORS V<br/>[FR] MODULATEURS MGLUR5 V
    申请人:ASTRAZENECA AB
    公开号:WO2007130824A2
    公开(公告)日:2007-11-15
    [EN] The present invention is directed to novel compounds, to a process for their preparation, their use in therapy and pharmaceutical compositions comprising the novel compounds.
    [FR] L'invention concerne de nouveaux composés, un procédé de préparation de ces derniers, leur utilisation en thérapie et des compositions pharmaceutiques renfermant les nouveaux composés précités.
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