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ethyl 4-(3-iodophenyl)-2,4-dioxobutanoate | 925940-90-5

中文名称
——
中文别名
——
英文名称
ethyl 4-(3-iodophenyl)-2,4-dioxobutanoate
英文别名
4-(3-iodophenyl)-2,4-dioxo-butyric acid ethyl ester
ethyl 4-(3-iodophenyl)-2,4-dioxobutanoate化学式
CAS
925940-90-5
化学式
C12H11IO4
mdl
——
分子量
346.121
InChiKey
JTPUHDGFYQNILA-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):
    2.5
  • 重原子数:
    17
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.25
  • 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:
    ethyl 4-(3-iodophenyl)-2,4-dioxobutanoate 在 sodium dithionite 、 溶剂黄146 作用下, 以 乙醇 为溶剂, 反应 36.0h, 生成 ethyl 3-amino-6-(3-iodophenyl)-2-methylisonicotinate
    参考文献:
    名称:
    [EN] SMALL MOLECULE INHIBITORS OF NF-kB INDUCING KINASE
    [FR] INHIBITEURS À PETITE MOLÉCULE DE KINASE INDUISANT NF-KB
    摘要:
    本发明涉及抑制NIK的化合物,以及包含这些化合物的药物组合物和使用方法。这些化合物和药物组合物预期能用于预防或治疗癌症(如包括白血病、淋巴瘤和多发性骨髓瘤的B细胞恶性肿瘤)、炎症性疾病、自身免疫疾病、免疫皮肤病学疾病(如掌跖脓疱病和化脓性汗腺炎)以及代谢紊乱疾病(如肥胖和糖尿病)。
    公开号:
    WO2020239999A1
  • 作为产物:
    描述:
    3-碘苯乙酮草酸二乙酯sodium methylate 作用下, 以 甲醇 为溶剂, 反应 16.0h, 生成 ethyl 4-(3-iodophenyl)-2,4-dioxobutanoate
    参考文献:
    名称:
    [123I]-Celecoxib Analogues as SPECT Tracers of Cyclooxygenase-2 in Inflammation
    摘要:
    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.
    DOI:
    10.1021/ml100232q
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文献信息

  • MgluR5 modulators
    申请人:Isaac Methvin
    公开号:US20080125436A1
    公开(公告)日:2008-05-29
    The present invention is directed to compounds of formula I: Wherein R 1 to R 5 , X and Z are further defined in the description. The invention also relates to processes for the preparation of the compounds and to intermediates used in the preparation, pharmaceutical compositions containing the compounds, and to the use of the compounds in therapy.
    本发明涉及式I的化合物:其中R1至R5、X和Z在说明书中进一步定义。本发明还涉及制备该化合物的过程,以及用于制备中间体的中间体,含有该化合物的制药组合物,以及在治疗中使用该化合物。
  • US7772235B2
    申请人:——
    公开号:US7772235B2
    公开(公告)日:2010-08-10
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