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2,3,4,6-Tetramethylpyridin-1-ium;perchlorate

中文名称
——
中文别名
——
英文名称
2,3,4,6-Tetramethylpyridin-1-ium;perchlorate
英文别名
2,3,4,6-tetramethylpyridin-1-ium;perchlorate
2,3,4,6-Tetramethylpyridin-1-ium;perchlorate化学式
CAS
——
化学式
C9H14ClNO4
mdl
——
分子量
235.66
InChiKey
BOPGESYEWLJRON-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):
    -1.81
  • 重原子数:
    15
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    84.3
  • 氢给体数:
    1
  • 氢受体数:
    5

文献信息

  • CA IX-SPECIFIC INHIBITORS
    申请人:INSTITUTE OF VIROLOGY
    公开号:EP1569633A2
    公开(公告)日:2005-09-07
  • EP1569633A4
    申请人:——
    公开号:EP1569633A4
    公开(公告)日:2008-03-05
  • [EN] CA IX-SPECIFIC INHIBITORS<br/>[FR] INHIBITEURS SPECIFIQUES DE CA IX
    申请人:BAYER HEALTHCARE
    公开号:WO2004048544A2
    公开(公告)日:2004-06-10
    Therapeutic methods for inhibiting the growth of preneoplastic/ neoplastic vertebrate cells that abnormally express MN protein are disclosed. Screening assays are provided for identifying compounds, preferably membraneimpermeant compounds, which inhibit the enzymatic activity of MN protein/ polypeptides and that are useful for treating patients with preneoplastic/neoplastic disease. Further methods are disclosed for the preparation of positively-charged, membrane-impermeant heterocyclic sulfonamide CA inhibitors with high affinity for the membrane-bound carbonic anhydrase CA IX. Preferred CA IX-specific inhibitors are aromatic and heterocylic sulfonamides, preferably that are membraneimpermeant. Particularly preferred CA IX-specific inhibitors are pyridinium derivatives of such aromatic and heterocyclic sulfonamides. The CA IX-specific inhibitors of the invention can also be used diagnostically/prognostically for preneoplastic/neoplastic disease, and for imaging use, for example, to detect precancerous cells, tumors and/or metastases. The CA IX-specific inhibitors can be labelled or conjugated to radioisotopes for radiotherapy. The CA IX-specific inhibitors may be combined with conventional therapeutic anti­cancer drugs, with other different inhibitors of cancer-related pathways, with bioreductive drugs, or with radiotherapy to enhance the efficiency of each treatment. The CA IX-specific inhibitors may also be combined with CA IX-specific antibodies, preferably monoclonal antibodies or biologically active antibody fragments, more preferably humanized or fully human CA IX monoclonal antibodies or biologically active fragments or such monoclonal antibodies. Still further, the CA IX-specific inhibitors can be used for gene therapy coupled to vectors for targeted delivery to preneoplastic/neoplastic cells expressing CA IX on their surfaces.
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