| 1220040-70-9

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 大环内酰胺类
• CAS: 1220040-70-9
• 化学式: C₄₃H₅₈N₄O₁₂
• 分子量: 821.942
• InChiKey: JQXXHWHPUNPDRT-VIZBMLMOSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.34
• 重原子数：
  59.0
• 可旋转键数：
  4.0
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.53
• 拓扑面积：
  220.15
• 氢给体数：
  6.0
• 氢受体数：
  15.0

反应信息

• 作为产物：
  描述：

  [11C]methyl iodide 、 N-去甲利福平 在 potassium carbonate 作用下， 以 二甲基亚砜 、 乙腈 为溶剂， 反应 0.17h， 生成
  参考文献：
  名称：

  Radiosynthesis and Bioimaging of the Tuberculosis Chemotherapeutics Isoniazid, Rifampicin and Pyrazinamide in Baboons

  摘要：

  The front-line tuberculosis (TB) chemotherapeutics isoniazid (INH), rifampicin (RIF), and pyrazinamide (PZA) have been labeled with carbon-11 and the biodistribution of each labeled drug has been determined in baboons using positron emission tomography (PET). Each radiosynthesis and formulation has been accomplished in 1 h, using [C-11]CH3I to label RIF and [C-11]HCN to label INH and PZA. Following iv administration, INH, PZA, RIF, and/or their radiolabeled metabolites clear rapidly from many tissues; however, INH, PZA, and/or their radiolabeled metabolites accumulate in the bladder while RIF and/or its radiolabeled metabolites accumulates in the liver and gall bladder, consistent with the known routes of excretion of the drugs. In addition, the biodistribution data demonstrate that the ability of the three drugs and their radiolabeled metabolites to cross the blood brain barrier decreases in the order PZA > INH > RIF, although in all cases the estimated drug concentrations are greater than the minimum inhibitory concentration (MIC) values for inhibiting bacterial growth of Mycobacterium tuberculosis (MTB). The pharmacokinetic (PK) and drug distribution data have important implications for treatment of disseminated TB in the brain and pave the way for imaging the distribution of the pathogen in vivo.

  DOI：

  10.1021/jm901858n