5-(2-bromoethylthio)selenophene-2-carbonitrile | 1297906-72-9

• 分子结构分类: 有机化合物 - 有机硫化合物 - 硫醚类
• 英文名称: 5-(2-bromoethylthio)selenophene-2-carbonitrile
• 英文别名: 5-(2-Bromoethylsulfanyl)selenophene-2-carbonitrile
• CAS: 1297906-72-9
• 化学式: C₇H₆BrNSSe
• 分子量: 295.061
• InChiKey: XCEPYFYAMIRCTI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.1
• 重原子数：
  11
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.29
• 拓扑面积：
  49.1
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  5-(2-bromoethylthio)selenophene-2-carbonitrile 在 sodium tetrahydroborate 、 potassium carbonate 、 potassium iodide 作用下， 以 四氢呋喃 、 甲醇 、 N,N-二甲基甲酰胺 为溶剂， 生成 (3R,4R)-methyl 1-(2-(5-cyanoselenophen-2-ylthio)ethyl)-4-(3-hydroxy-3-(6-methoxyquinolin-4-yl)propyl)piperidine-3-carboxylate
  参考文献：
  名称：

  Selenophene-Containing Inhibitors of Type IIA Bacterial Topoisomerases

  摘要：

  We investigated compounds related to the previously reported anti-staphyloccocal agent AVE6971 in an effort to attenuate inhibition of hERG potassium channel current that has been noted for this and related antibacterial drug classes. While most modifications of the original thiophene group compromised antibacterial activity, one selenophene analogue displayed (i) improved activity against the primary target enzyme DNA gyrase, (ii) similar activities against a panel of MRSA clinical isolates, and (iii) reduced hERG channel inhibition.

  DOI：

  10.1021/jm2002124
• 作为产物：
  描述：

  (2-bromoethyl)(selenophen-2-yl)sulfane 在 ammonium hydroxide 、 碘 、 三氯氧磷 作用下， 以 四氢呋喃 、 水 为溶剂， 反应 2.0h， 生成 5-(2-bromoethylthio)selenophene-2-carbonitrile
  参考文献：
  名称：

  Selenophene-Containing Inhibitors of Type IIA Bacterial Topoisomerases

  摘要：

  We investigated compounds related to the previously reported anti-staphyloccocal agent AVE6971 in an effort to attenuate inhibition of hERG potassium channel current that has been noted for this and related antibacterial drug classes. While most modifications of the original thiophene group compromised antibacterial activity, one selenophene analogue displayed (i) improved activity against the primary target enzyme DNA gyrase, (ii) similar activities against a panel of MRSA clinical isolates, and (iii) reduced hERG channel inhibition.

  DOI：

  10.1021/jm2002124

文献信息

• Selenophene-Containing Inhibitors of Type IIA Bacterial Topoisomerases
  作者：Jason A. Wiles、Avinash S. Phadke、Barton J. Bradbury、Michael J. Pucci、Jane A. Thanassi、Milind Deshpande

  DOI：10.1021/jm2002124

  日期：2011.5.12

  We investigated compounds related to the previously reported anti-staphyloccocal agent AVE6971 in an effort to attenuate inhibition of hERG potassium channel current that has been noted for this and related antibacterial drug classes. While most modifications of the original thiophene group compromised antibacterial activity, one selenophene analogue displayed (i) improved activity against the primary target enzyme DNA gyrase, (ii) similar activities against a panel of MRSA clinical isolates, and (iii) reduced hERG channel inhibition.