descarboxymoxifloxacin | 1322062-62-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 喹啉及其衍生物
• 英文名称: descarboxymoxifloxacin
• 英文别名: Descarboxyulifloxacin；6-fluoro-1-methyl-7-piperazin-1-yl-1H-[1,3]thiazeto[3,2-a]quinolin-4-one
• CAS: 1322062-62-3
• 化学式: C₁₅H₁₆FN₃OS
• 分子量: 305.376
• InChiKey: FUNGBOLAQYFHTK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.3
• 重原子数：
  21
• 可旋转键数：
  1
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  60.9
• 氢给体数：
  1
• 氢受体数：
  6

反应信息

• 作为产物：
  描述：

  6-氟-7-哌嗪-1-甲基-4-氧-[1,3]硫氮杂环[3,2-a]-喹啉-3-羧酸 在 硫酸 、 水 作用下， 反应 144.0h， 以40%的产率得到descarboxymoxifloxacin
  参考文献：
  名称：

  Synthesis and evaluation of 1-cyclopropyl-2-thioalkyl-8-methoxy fluoroquinolones

  摘要：

  Novel fluoroquinolone derivatives substituted with a 2-thioalkyl moiety, with and without a concomitant 3-carboxylate group, were synthesized to evaluate the effect of C-2 thioalkyl substituents on gyrase binding and inhibition. The presence of a 2-thioalkyl group universally decreased activity as compared to parent fluoroquinolones. However, with derivatives of moxifloxacin the presence of either a 2-thioalkyl group or a 3-carboxylate moiety increased activity over the 2,3-unsubstituted derivative. Energy minimization of structures provides an explanation for relative activities of fluoroquinolones having a C-2 thio moiety. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2011.05.112

文献信息

• Synthesis and evaluation of 1-cyclopropyl-2-thioalkyl-8-methoxy fluoroquinolones
  作者：Kevin R. Marks、Muhammad Malik、Arkady Mustaev、Hiroshi Hiasa、Karl Drlica、Robert J. Kerns

  DOI：10.1016/j.bmcl.2011.05.112

  日期：2011.8

  Novel fluoroquinolone derivatives substituted with a 2-thioalkyl moiety, with and without a concomitant 3-carboxylate group, were synthesized to evaluate the effect of C-2 thioalkyl substituents on gyrase binding and inhibition. The presence of a 2-thioalkyl group universally decreased activity as compared to parent fluoroquinolones. However, with derivatives of moxifloxacin the presence of either a 2-thioalkyl group or a 3-carboxylate moiety increased activity over the 2,3-unsubstituted derivative. Energy minimization of structures provides an explanation for relative activities of fluoroquinolones having a C-2 thio moiety. (C) 2011 Elsevier Ltd. All rights reserved.